US20070148761A1 - Instrument for monitoring polymerase chain reaction of DNA - Google Patents

Abstract

An optical instrument monitors PCR replication of DNA in a reaction apparatus having vials of reaction ingredients. A beam splitter passes an excitation beam to the vials. An emission beam from the reaction ingredients can be passed by the beam splitter to a detector from which a processor can compute DNA concentration. A reference strip with a plurality of reference emitters can be provided which emits reference beams of different intensity, from which the processor can select an optimum emitter for compensating for drift. Exposure time can be automatically adjusted for keeping within optimum dynamic ranges of the detector and processor. A module of the beam splitter and associated optical filters can be associated with a selected dye, and can be replaceable for different dyes.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS
• The present application is a continuation of U.S. patent application Ser. No. 10/370,846, filed Feb. 20, 2003, which in turn is a continuation of U.S. patent application Ser. No. 09/700,536, filed Nov. 29, 2001, which is a National Phase Application Under 35 U.S.C. §371 of PCT International Application No. PCT/US99/11088, filed on May 17, 1999, which claims priority from U.S. Patent Provisional Application No. 60/085,765, filed May 16, 1998, and U.S. Provisional Patent Application No. 60/092,784, filed Jul. 14, 1998. U.S. patent application Ser. No. 10/216,620, filed Aug. 9, 2002 is a related application. All of the above-identified applications are hereby incorporated herein in their entireties by reference.
• This invention relates to biochemical analyses, and particularly to quantitative monitoring of DNA during a polymerase chain reaction (PCR) process.
BACKGROUND
• Polymerase chain reaction (PCR) is a process for amplifying or multiplying quantities of double-stranded deoxyribonucleic acid (DNA). In a PCR apparatus, a thermal cycler block has one or more wells for holding vials containing a suspension of ingredients for a reaction to produce more DNA starting with “seed” samples of the DNA. The starting ingredients in an aqueous suspension, in addition to the a seed sample, include selected DNA primer strands, DNA elements, enzymes and other chemicals. The temperature of the block is cycled between a lower temperature extension phase of the PCR reaction at about 60° C., which is the phase where all of the DNA strands have recombined into double strands, and a high temperature denaturing phase at about 95° C., during which the DNA is denatured or split into single strands. Such a temperature program essentially doubles the DNA in each cycle, thus providing a method for replicating significant amounts of the DNA from a small starting quantity. The PCR process is taught, for example, in U.S. Pat. No. 4,683,202.
• Quantitative measurements have been made on the DNA production during the PCR process, to provide measures of the starting amount and the amount produced. Measurements and computation techniques are taught in U.S. Pat. No. 5,766,889 (Atwood), as well as in an article “Kinetic PCR Analysis: Real-time Monitoring of DNA Amplification Reactions” by Russel Higuchi, et al., Bio/Technology vol. 11, pp. 1026-1030 (September 1993), and an article “Product Differentiation by Analysis of DNA Melting Curves during the Polymerase Chain Reaction” by Kirk M. Ririe, et al., Analytical Biochemistry vol. 245, pp. 154-160 (1997).
• Prior measuring techniques have utilized microvolume fluorometers (spectrofluorometers) and a simple arrangement of a video camera with illumination lamps. Such apparatus utilize dyes that fluoresce in the presence of double-stranded DNA. These techniques and instruments are not particularly adapted to PCR apparatus for routine monitoring of the reaction. There also is a need for greater precision during the monitoring and measurements. Previous instruments that allow real time acquisition and analysis of PCR data have been very basic devices without the required dynamic range, do not have built-in calibration means, do not allow operation with sample well caps, or are very expensive.
• An object of the present invention is to provide a novel optical instrument for quantitative monitoring of DNA replication in a PCR apparatus. Other objects are to provide such an instrument with improved dynamic range, automatic selection of exposure time to extend dynamic range, automatic adjustment for drift, simplified operation, relatively low cost, and easy changing of optics to accommodate different fluorescent dyes.
SUMMARY
• The foregoing and other objects are achieved, at least in part, by an optical instrument as described herein for monitoring polymerase chain reaction replication of DNA. The replication is in a reaction apparatus that includes a thermal cycler block for holding at least one vial containing a suspension of ingredients for the reaction. The ingredients include a fluorescent dye that fluoresces proportionately in presence of DNA.
• The instrument includes a light source, means for directing light beams, a light detector, and means for processing data signals. The light source emits a source beam having at least a primary excitation frequency that causes the dye to fluoresce at an emission frequency. A first means is disposed to be receptive of the source beam to effect an excitation beam having the excitation frequency. A primary focusing means is disposed to focus the excitation beam into each suspension such that the primary dye emits an emission beam having the emission frequency and an intensity representative of concentration of DNA in each suspension. The focusing means is receptive of and passes the emission beam. A second means is disposed to be receptive of the emission beam from the focusing means so as to further pass the emission beam at the emission frequency to another focusing means that focuses the emission beam onto a detector. The detector generates primary data signals representative of the emission beam and thereby a corresponding concentration of DNA in each vial. A processor is receptive of the primary data signals for computing and displaying the concentration of DNA.
• In a preferred embodiment, the first means and the second means together comprise a beam splitter that is receptive of the source beam to effect the excitation beam, and receptive of the emission beam to pass the emission beam to the detector. The block is configured to hold a plurality of vials, and the focusing means comprises a corresponding plurality of vial lenses each disposed over a vial such that the emission beam comprises individual beams each associated with a vial. The focusing means may further comprise a field lens such as a Fresnel lens disposed cooperatively with the vial lenses to effect focusing of the excitation beam into each suspension, and to pass the individual beams to the second means (beam splitter). The detector preferably comprises an array of photoreceptors receptive of the individual beams to generate corresponding data signals such that the processing means computes concentration of DNA in each vial.
• The instrument should also include an excitation filter between the light source and the beam splitter, and an emission filter between the beam splitter and the detector. The splitter and filters are associated with a selected primary dye in the suspension. In a further embodiment, a filter module contains the splitter and filters, and the module is removable from the housing for replacement with another module associated with another selected primary dye.
• For a reference, a fluorescent reference member emits reference light in response to the excitation beam. The reference is disposed to be receptive of a portion of the excitation beam from the first means. A portion of the reference light is passed by the second means as a reference beam to the detector, so as to generate reference signals for utilization in the computing of the concentration of DNA. Preferably the reference member comprises a plurality of reference emitters, each emitting a reference beam of different intensity in response to the excitation beam, to allow selection by the processor of a reference set having the highest data signals that are less than a predetermined maximum that is less than the saturation limit.
• The detector is operatively connected to the processing means for the detector to integrate emission beam input over a preselected exposure time for generating each set of data signals, and the processing means or the detector or a combination thereof have a saturation limit for the data signals. In a further aspect of the invention, the processing means comprises adjustment means for automatically effecting adjustments in exposure time to maintain the primary data within a predetermined operating range for maintaining corresponding data signals less than the saturation limit, and means for correcting the primary data in proportion to the adjustments in exposure time. Preferably, the processor computes photoreceptor data from the data signals for each photoreceptor, and the adjustment means ascertains highest photoreceptor data, determines whether the highest photoreceptor data are less than, within or higher than the predetermined operating range and, based on such determination, the exposure time is increased, retained or reduced so as to effect a subsequent exposure time for maintaining subsequent photoreceptor data within the predetermined operating range.
BRIEF DESCRIPTION OF THE DRAWINGS
• FIG. 1 is a schematic of an optical train for an optical instrument according to the invention, associated with a polymerase chain reaction (PCR) reaction apparatus.
• FIG. 2 is a perspective of the instrument ofFIG. 1 with a side panel removed.
• FIG. 3 is an exploded perspective of a module shown inFIG. 2.
• FIG. 4 is a perspective of a reference member in the optical train ofFIG. 1.
• FIG. 5 is a flow chart for computing DNA concentration from data obtained with the instrument ofFIG. 1.
• FIG. 6 is a flow chart for determining exposure time for data acquisition in operation of the instrument ofFIG. 1 and for computations in the flow chart ofFIG. 5.
• FIG. 7 is a graph of extension phase data of fluorescence vs. cycles from operation of the instrument ofFIG. 1 with a PCR apparatus.
• FIG. 8 is a flow chart for computing secondary data for computations in the flow chart ofFIG. 5.
• FIG. 9 is a flow chart for computing ratios between the plurality of reference emitter segments of the reference member ofFIG. 4.
DETAILED DESCRIPTION
• An optical instrument A of the invention is utilized with or incorporated into a reaction apparatus B that replicates (“amplifies”) selected portions of DNA by polymerase chain reaction (“PCR”). The reaction apparatus is conventional and should function without interference from the instrument which monitors the amount of DNA in real time during replication. Suitable reaction apparatus are described in U.S. Pat. Nos. 5,475,610 and 5,656,493.
• The reaction apparatus (FIG. 1) is conventional and has two main components, namely athermal cycler block1 with wells1afor holding at least onevial1bcontaining a suspension of ingredients for the reaction, and a thermal cycle controller1cfor cycling the temperature of the block through a specified temperature program. The starting ingredients of the aqueous suspension of sample materials include a “seed” sample of DNA, selected DNA primer strands, DNA elements, enzymes and other chemicals. The block, typically aluminum, is heated and cooled in a prescribed cycle by electrical means, liquid or air coolant, or a combination of these, or other means to achieve the cycling.
• The suspensions in the vials are thereby cycled between two temperature phases so as to effect the polymerase chain reaction. These phases are a lower temperature extension phase of the PCR reaction at about 60° C., which is the phase where all of the DNA strands have recombined into double strands, and a high temperature denaturing phase at about 95° C., during which the DNA is denatured or split into single strands.
• For the present purpose the sample also contains a fluorescent dye that fluoresces proportionately and more strongly in the presence of double stranded DNA to which the dye binds, for example SYBR Green dye (available from Molecular Probes, Inc., Eugene, Oreg.) that fluoresces in the presence of double stranded DNA. Another type of fluorescent dye labeled “probes”, which are DNA-like structures with complimentary sequences to selected DNA strand portions, may also be used. Other dyes that have similar characteristics may be utilized. As used herein and in the claims, the term “marker dye” refers to the type that binds to double stranded DNA, or to the probe type, or to any other type of dye that attaches to DNA so as to fluoresce in proportion to the quantity of DNA. Samples may also contain an additional, passive dye (independent of the DNA) to serve as a reference as described below. Under incidence of light having a correct excitation frequency, generally a dye fluoresces to emit light at an emission frequency that is lower than that of the excitation light.
• The vials typically are formed conically in a plastic unitary tray containing a plurality of vials, for example 96 in an array of 12 by 8. The tray preferably is removable from the block for preparations. A plastic unitary cover withcaps1dfor the vials may rest or attach over the vials to prevent contamination and evaporation loss. Other means may be used for this function, such as oil on the sample surface, in which case caps are not needed. If used, the caps are transparent to light utilized in the instrument, and may be convex facing upwardly.
• The monitoring instrument is mounted over the block containing the vials. The instrument is removable or swings away for access to the vials. In the bottom of the instrument, aplaten2 rests over the vial caps or, if none, directly over the vials. The platen, advantageously aluminum, has an array of holes2atherethrough aligned with the vials, each hole having a diameter about the same as the vial top diameter. If there are caps, the platen should have its temperature maintained by a film heater or other means for heating the platen sufficiently to prevent condensation under the caps without interfering with DNA replication in the vials, for example holding the platen at slightly higher temperature than the highest sample temperature that the thermal cycler reaches.
• Above each of the vials is alens2bpositioned for its focal point to be approximately centered in the suspension in the vial. Above these lenses is afield lens3 to provide a telecentric optical system. Advantageously the field lens is an aspherically corrected Fresnel lens for minimal distortion. A neutral density pattern (not shown) to correct nonuniformities in illumination and imaging may be mounted on or in proximity to the field lens, for example to attenuate light in the center of the image field. A folding optical mirror is optionally mounted at 45° for convenient packaging. This may be omitted, or other such folding optics may be used. Also the field lens, and/or the vial lenses, each may be comprised of two or more lenses that effect the required focusing, the word “lens” herein including such multiplicities.
• Alight source11 for asource beam20 of light is provided, for example a 100 watt halogen lamp. Preferably this is mounted at a focal distance of an ellipsoid reflector11awhich produces a relatively uniform pattern over the desired area. Also, advantageously, the reflector should be dichroic, i.e. substantially reflecting visible light and transmitting infrared light, to restrict infrared from the other optical components and from overheating the instrument. This is further aided by aheat reflecting mirror13 in the optical path. A mechanical orelectronic shutter12 allows blockage of the light source for obtaining dark data. The type of light source is not critical, and other types may be used such as a projection lamp or a laser, with appropriate optical elements.
• Abeam splitter6 is disposed to receive thesource beam20. In the present embodiment this is a dichroic reflector such that, positioned at 45°, it reflects light having an excitation frequency that causes the marker dye to fluoresce at an emission frequency, and passes light having the emission frequency. Such a conventional optical device typically utilizes optical interference layers to provide the specific frequency response.
• The beam splitter is positioned to reflect the source beam to the folding mirror. The source beam is reflected from the splitter as aexcitation beam22 having substantially the excitation frequency. The excitation beam is focused by thefield lens3 and then as separatedbeams24 by the vial (well)lenses2b into the center of the vials. The marker dye is thereby caused to emit light at the emission frequency. This light is passed upwardly as an emission beam in the form ofindividual beams26 that are reflected from thefolding mirror5 to thebeam splitter6 which passes the emission beam through to adetector10.
• Together thevial lenses2band thefield lens3 constitute a primary focusing means for focusing both the excitation beam and the emission beam. In an alternative aspect, the field lens may be omitted so that the focusing means consists only of thevial lenses2b. Alternatively, the vial lenses may be omitted so that the focusing means consists only of an objective lens in the field lens position to focus the individual emission beams on the detector.
• Also, alternatively, thebeam splitter6 may pass the source beam as an excitation beam and reflect the emission beam, with appropriate rearrangement of the lamp and the detector. Moreover, other angles than 45° could be used if more suitable for the beam splitter, such as a more perpendicular reflection and pass through. More broadly, the beam splitter splits the optical paths for the excitation beam and the emission beam, and other variations that achieve this may be suitable It is desirable to minimize source light reaching the detector, which the dichroic device helps achieve. A non-dichroic beam splitter may be used but would be less efficient as significant source light may reach the detector, or may be reflected or transmitted in the wrong direction and lost
• To further filter the source light, anexcitation filter7 is disposed between thelight source11 and thebeam splitter6. This passes light having the excitation frequency and substantially blocks light having the emission frequency. Similarly, anemission filter8 is disposed between the beam splitter and the detector, in this case between the splitter and adetector lens9 in front of the detector. This filter passes light having the emission frequency and substantially blocks light having the excitation frequency. Although a detector lens is preferred, a focusing reflector may be substituted for the detector lens. Such an emission focusing means (detector lens or reflector) may be located after (as shown) or before the beam splitter and on either side of the emission filter, and alternatively may be integrated into the primary focusing means. For example, the field lens may be an objective lens that focuses the emission beam onto the detector.
• Suitable filters are conventional optical bandpass filters utilizing optical interference films, each having a bandpass at a frequency optimum either for excitation of the fluorescent dye or its emission. Each filter should have very high attenuation for the other (non-bandpass) frequency, in order to prevent “ghost” images from reflected and stray light. For SYBR Green dye, for example, the excitation filter bandpass should center around 485 nm wavelength, and the emission filter bandpass should center around 555 nm. The beam splitter should transition from reflection to transmission between these two, e.g. about 510 nm, so that light less than this wavelength is reflected and higher wavelength light is passed through.
• More broadly, the excitation filter and the beam splitter together constitute a first means disposed to be receptive of the source beam to effect an excitation beam having the excitation frequency, and the emission filter and the beam splitter together constitute a second means disposed to be receptive of the emission beam from the focusing means so as to pass the emission beam at the emission frequency to the detector. Also, as mentioned above, the beam splitter alternatively may pass the source beam as an excitation beam and reflect the emission beam to the detector. In another aspect, the fillers may be omitted, and the first means is represented by the beam splitter effecting the exitation beam from the source beam, and the second means is represented by the beam splitter passing the emission beam to the detector.
• In another arrangement, the beam splitter may be omitted, and the first means may constitute an excitation filter for the excitation frequency, the second means may constitute an emission filter for the emission frequency, with the light source and the detector being side by side so that the excitation and emission beams are on slightly different optical paths angularly. The source and detecton need not actually be side by side with one or more folding mirrors. Thus any such arrangement for achieving the effects described herein should be deemed equivalent. However, use of the beam splitter is preferred so that the excitation and emission beams through the field lens will have the same optical path.
• Advantageously thebeam splitter6, theexcitation filter7 and theemission filter8 are affixed in a module30 (FIG. 2) that is associated with a selected primary dye for the suspension. The module is removable from thehousing32 of the instrument A for replacement with another module containing different beam splitter and filters associated with another selected primary dye. The instrument includes alamp subhousing33 and acamera subhousing35.
• In an example (FIG. 3), each module includes a mountingblock34 with aflange36 that is affixable to the housing with asingle screw38. Thebeam splitter6 is held at 45° in the block with aframe40 and screws42. Theemission filter8 mounts (e.g. with glue) into the block. Theexcitation filter7 mounts similarly into a mountingmember44 that is held byscrews46 to the block. With the module in place, the instrument is closed up with aside plate47 that is screwed on. Positioning pins (not shown) ensure repeatable alignment. The replacement module may have the same mounting block and associated components, with the beam splitter and filters replaced.
• The detector lens9 (FIG. 1) is cooperative with thevial lenses2band thefield lens3 to focus the individual beams on thedetector10. The lens should be large aperture, low distortion and minimum vignetting.
• The detector preferably is an array detector, for example a charge injection device (CID) or, preferably, a charge coupled device (CCD). A conventional video camera containing a CCD detector, the detector lens and associated electronics for the detector should be suitable, such as an Electrim model 1000L which has751 active pixels horizontal and242 (non-interlaced) active pixels vertical. This camera includes a circuit board that directly interfaces to a computer ISA bus. No framegrabber circuitry is required with this camera. Essentially any other digital imaging device or subsystem may be used or adapted that is capable of taking still or freeze-frame images for post processing in a computer.
• A detector with a multiplicity of photoreceptors (pixels)78 is preferable if there are a plurality of vials, to provide separate monitoring of each. Alternatively a scanning device may be used with a single photodetector, for example by scanning the folding mirror and using a small aperture to the detector. Also, a simple device such as a photomultipier may be used if there is only one vial. A CCD receives light for a selected integration period and, after analog/digital conversion, reads out digital signal data at a level accumulated in this period. The integration is effectively controlled by an electronic shutter, and a frame transfer circuit is desirable. Signal data are generated for each pixel, including those receiving the individual beams of emitted light from the vials.
• The instrument preferably includes afluorescent reference member4 that emits reference light in response to the excitation beam. Advantageously the reference member is formed of a plurality of reference emitters, e.g. 6, each emitting a reference beam of different intensity in response to the excitation beam. The range of these intensities should approximate the range of intensities expected from the marker dye in the vials; for example each segment may be separated in brightness by about a factor of 2.5. The reference member is disposed to receive a portion of the excitation beam from the beam splitter. A good location is adjacent to the field lens, so that the optical paths associated with the member approximate those of the vials. Most of the reference light passes back through the beam splitter as a reference beam to the detector. The detector pixels receive the emission beam to generate reference signals for utilization along with the data signals in the computing of the concentration of DNA.
• Advantageously the reference member4 (FIG. 4) comprises a plasticfluorescent strip4aand aneutral density filter4bmounted over the fluorescent strip, optionally with anair space4hbetween, such that a portion of the excitation beam and the reference beam are attenuated by the neutral density filter. The neutral density filter has a series of densities4cto effect the plurality of reference emitters (segments) each emitting a reference beam of different intensity. A heating strip4dand an aluminum strip4gto smooth the heating are mounted in atrough4eon the bottom thereof, and the fluorescent strip is mounted on the aluminum strip over the heating strip. To prevent heat loss, this assembly preferably is covered by a transparent plexiglass window (not shown, so as to display the varying density filter). To help maintain constant fluorescence, the heating strip is controlled to maintain the fluorescent strip at a constant temperature against the thermal cycles of the cycler block and other effects. This is done because most fluorescent materials change in fluorescence inversely with temperature.
• The computer processor14 (FIG. 1) may be a conventional PC. The computer programming is conventional such as with “C”. Adaptations of the programming for the present invention will be readily recognized and achieved by those skilled in the art. The processor selectively processes signals from pixels receiving light from the vials and the reference emitters, ignoring surrounding light. The programming therefore advantageously includes masking to define the pixel regions of interest (ROI), e.g. as disclosed in copending provisional patent application Ser. No. 60/092,785 filed Jul. 14, 1998 of the present assignee. Mechanical alignment of the optics may be necessary to cooperatively focus the beams into the programmed regions of interest. The analog data signals are fed to the processor through an analog/digital (A/D)device15 which, for the present purpose, is considered to be pain of the processor A saturation level is proscribed by either the detector or the A/D or, preferably, the CCD dynamic range is matched to the A/D dynamic range. A suitable range is 8 bits of precision (256 levels), and the CCD amplifier offset is set so that the dark signal output of the CCD (with theshutter12 closed) is within the A/D range. The processor instructs the detector with selected exposure time to maintain the output within the dynamic range.
• In a typical operation, fluorescence data are taken from the plurality of vials (e.g. 96 regions of interest) and from the reference emitter segments, for each cycle in a DNA reaction replication sequence of thermal cycles, typically 40 to 50. Two data sets are taken (FIG. 5) for each thermal cycle during the extension phase of the PCR reaction at about 60° C., which is the phase where all of the DNA strands have recombined into double strands. One set is normal primary data50 (along with reference data described below) and the other isdark signal data51 with the mechanical shutter closed. Both digital data sets50,51 are converted by the A/D15 from respective analog data signals48,49 from the detector. The dark are subtracted55 from the normal, to yield dark-correcteddata57. In a simple procedure, the subtraction is pixel by pixel. Alternatively, total dark for each region of interest are subtracted from corresponding total fluorescence data. In another alternative, in order to increase effective dynamic range, it is advantageous to collect multiple exposures during each exposure period, e.g. 4 or 8 exposures. This is done by collecting multiple normal exposures and dark signal data for each pixel, subtracting each respective dark image from the normal data, then adding the subtracted data together to yield the primary data. This improves the statistical validity of the image data and increases its effective dynamic range.
• Data are taken simultaneously from the reference strip which has, for example, 6 segments together with the 96 vials for a total of 102 regions of interest. Preferably the processing means provides for automatic adjustment of the exposure time to maintain the data signals within a predetermined operating range that is less than the saturation limit during the DNA replication sequence, for example 35% to 70% of saturation. Computations for DNA concentration include corrections in proportion to adjustments in exposure time (FIG. 6).Signal data50,51 from eachexposure52,53 are obtained during a previously determinedexposure time54 by totaling the pixel counts within each region of interest (ROI).
• To provide the time adjustments, thehighest signal data56, which is data from one or more highest pixel readings, such as the three highest-reading contiguous pixels, is searched out58 from the corresponding data signals50. From acomparison62 it is determined whether the highest signal data are less than, within or higher than the selectedoperating range60. Based on such determination, the exposure time is adjusted64, i.e. increased, retained or reduced, to obtain thesubsequent exposure time66. A reference time68 (FIG. 5) also is selected which may be, for example, an initial time or a fixed standard time such as 1024 ms. The dark-correcteddata57 is time-corrected69 to yield correctedprimary data71, dividing by ratio of actual exposure time to the reference time. The first several cycles may be out of range, and thereafter a useful fluorescence curve should be obtained (FIG. 7).
• For the reference emitter, from the pixels receiving light from the reference strip4 (FIGS. 1 and 4) reference data signals73 are generated and converted by the A/D15 toreference data72. Selectedreference data74 from a specific reference segment4c(FIG. 4) are selected76 as that data having the highest signal strength that is less than a predetermined maximum77 that, in turn, is less than the saturation limit, e.g. 70%. A next dimmer segment is also selected75, and the selectedreference data74 include the data from that segment. Thedark data51 are subtracted78 from thereference data74, and the dark-correcteddata80 are adjusted84 forexposure time54 to yield adjustedreference data82.
• Thedata82 includes dark correcteddata82′ for the highest segment and dark correcteddata82″ for the next dimmer segment (FIG. 9). The ratios of brightness between each segment are computed89 and built up over the course of data collection. Each time data is collected, the ratio between the highest and next dimmer segment is calculated. As different optimum segments are selected on succeeding data collections, a table ofratios85 is assembled. Alternatively, these rations may be collected and calculated in advance.
• Thisadjusted reference data82′ (fromdata82,FIG. 5) are utilized for computing normalizedreference data88 which are normalized86 in real time as a ratio toreference data90 from an initial or other selected previous cycle in the DNA replication (PCR) sequence by working back with theratios85. The normalized reference data are utilized on the correctedprimary data71 in anormalization computation92 to provide drift normalizedprimary data94 by dividing the primary data by the normalized reference data. This corrects for instrument drift during the monitoring.DNA concentration96 may then be computed98 from a storedcalibration factors99, determined by running standard known DNA concentrations to determine the slope and intercept of a line relating starting concentration to the starting cycle of the growth curve (FIG. 7) as taught in the aforementioned article by Higuchi and U.S. Pat. No. 5,766,889. (Further normalization118,120 and baseline correction122-130 are discussed below.)
• Extension phase data for a typical PCR sequence would look likeFIG. 7, plotted for each PCR cycle. If desired, the data may be corrected for dye bleaching or other sample chemical effects by normalizing to sample vials containing samples with the same dye and with DNA amplification prevented chemically.
• The sample additionally may contain one or more types of dye molecules that serve as a “passive” reference having some fluorescence in the same wavelength range as the DNA binding dye. This reference dye is made up, for example, of a nucleic acid sequence labeled with Rhodamine and Fluorescein dye derivatives. A suitable reference is Rox dye from Perkin-Elmer Applied Biosystems. These passive dye molecules do not take part in the PCR reaction, so that their fluorescence is substantially without influence from DNA and remains constant during the reaction. This fluorescence can be used to normalize the fluorescence from the DNA binding dye with a standard concentration of passive dye included in the ingredients of at least one vial, preferably in every vial.
• The source beam includes a secondary excitation frequency that causes the passive dye to fluoresce at a secondary frequency and thereby emit a secondary beam directed to the detector to generate corresponding secondary data signals. The processor is receptive of the secondary data signals for computing secondary data representative of standard concentration. These data are used to normalize the primary data, so that the concentration of DNA is normalized to the standard concentration of passive dye after correcting computations of concentration of DNA in proportion to adjustments in exposure time, and in conjunction with the normalization for drift. Advantageously, and in the present example, the secondary excitation frequency is identical to the primary excitation frequency, and the passive dye fluoresces such that the emitted secondary beam is substantially at the emission frequency. The primary data signals are generated during each extension phase of cycling of the thermal cycler block when DNA is recombined and correspondingly primary dye emission is maximized. The secondary data signals are generated during each denature phase of cycling of the thermal cycler block when DNA is denatured and correspondingly primary dye emission is minimized. Thus data signals for the primary phase are substantially representative of DNA concentration, and data signals for the secondary phase are substantially representative of the standard concentration of passive dye.
• The dark and normal data are taken for the vial samples and the reference strip, and the dark is subtracted from the normal fluorescence data. This dark and normal data set is taken during the extension phase of the PCR reaction at about 60° C., which is the phase where all of the DNA strands have recombined into double strands. During this phase, the fluorescence from the DNA binding dye is maximized, and the fluorescence from the passive reference molecules is superimposed but much smaller. A separate dark and normal data set is taken during the high temperature (about 95° C.) denaturing phase, during which the DNA is denatured or split into single strands. During this phase, the fluorescence of the DNA binding dye is minimized, and almost non-existent, because the DNA is not double stranded and the fluorescence of the dyes used have a large decrease in fluorescence with increased temperature. Therefore the denaturing phase images substantially contain reference fluorescence from the passive reference molecules. The dark-corrected reference (denaturing) data set, after correction for measured temperature dependence, may be subtracted from the dark-corrected DNA binding dye data set, or may be deemed insignificant for the normal data set.
• Alternatively, it may be desirable to image the passive reference dye labeled molecules by taking the additional images, for each PCR cycle, using a separate optical bandpass filter that rejects wavelengths emitted by the DNA binding dye while accepting wavelengths from the passive reference dye. This data would be functionally equivalent to the denature data.
• Illustrating operation for the denature phase (FIG. 8), respective normal and dark data signals102,104 are obtained in the same manner as for the primary data, withnormal exposure52′ andclosed shutter53′.Exposure time106 may be the same as for an adjacent extension phase in the sequence, or determined from a previous denature phase run (as described with respect toFIG. 7), or may be a suitable time predetermined for all denature phases in the sequence. The A/D15 converts the signals tosecondary data108 anddark data110. The dark is subtracted55′ from the secondary to yield dark-correcteddata112 which is further corrected69′ with areference time114 and theactual exposure time106 to yield correctedsecondary data116.
• The extension cycle, drift normalizedprimary data94 then are normalized118 by dividing by the average of a selected number (e.g. 10) of cycles for the denature phase correctedsecondary data116 to produce further normalized fluorescence data or further normalizeddata120, which removes sample well to well non-uniformity effects. Cycle by cycle division may be used in place of an average. Alternatively the secondary data may be applied to the correctedprimary data71 before or after drift normalization. Baseline samples may be selected122 and averaged124 to producebaseline data126. The further normalizeddata120 are then divided128 by the baseline data to yield baseline correcteddata130. These baseline samples are selected so as to be before the PCR growth exceeds the nearly horizontal base line portion of the curve inFIG. 7. Selected baseline cycles may be, for example, cycles6 through15. Afterfurther normalization118, the further normalizeddata118 are used to compute98DNA concentration96
• The trend (e.g. least squares regression line) of these same baseline samples is subtracted from the normalized extension cycle data, to produce data that has a flat base line at zero. This data set may then be processed using established or other desired PCR methods to calculate the amount of starting copies of DNA. A simple procedure is to extrapolate for the inflection point at the transition from flat to rising. A more sophisticated procedure is described in the aforementioned U.S. Pat. No. 5,766,889.
• The data may be used for various purposes, for example quantitative monitoring of the reaction or determination of replicated DNA concentration, or determination of the starting amount. The instrument also may be used (with or without normalizations and other corrections) simply to display whether replication is taking place during a sequence, or has taken place.
• While the invention has been described above in detail with reference to specific embodiments, various changes and modifications which fall within the spirit of the invention and scope of the appended claims will become apparent to those skilled in this art. Therefore, the invention is intended only to be limited by the appended claims or their equivalents.

Claims (20)

1. An instrument comprising:

a plurality of spaced-apart vials;

a light source adapted to direct an excitation beam along an excitation beam path simultaneously toward each of the plurality of vials;

a beam splitter disposed along the excitation beam path between the light source and the plurality of vials;

a lens disposed along the excitation beam path between the light source and the plurality of vials; and

a detector disposed along an emission beam path and arranged to receive emission beams emitted from the plurality of vials and through the lens;

wherein the lens and the beam splitter are disposed along an emission beam path between the plurality of vials and the detector, and the beam splitter is arranged to split apart the excitation beam path and the emission beam path.

2. The instrument ofclaim 1, wherein the detector generates primary data signals representative of the emission beams.

3. The instrument ofclaim 2, further comprising a processor to receive the primary data signals and compute corresponding concentrations in the respective vials.

4. The instrument ofclaim 1, further comprising a detector lens disposed along an emission beam path, between the lens and the detector.

5. The instrument ofclaim 1, further comprising an excitation beam filter disposed along an excitation beam path between the light source and the lens.

6. The instrument ofclaim 1, further comprising an emission beam filter disposed along an emission beam path between the lens and the detector.

7. The instrument ofclaim 1, further comprising a fold mirror disposed along the excitation beam path, between the light source and the plurality of vials.

8. The instrument ofclaim 1, further comprising a plurality of focusing lenses disposed along excitation beam paths between the lens and the plurality of vials.

9. The instrument ofclaim 1, wherein the instrument is adapted to simultaneously direct a plurality of excitation beams respectively toward the plurality of vials.

10. The instrument ofclaim 1, further comprising reaction ingredients disposed in each of the plurality of vials.

11. The instrument ofclaim 10, wherein the reaction ingredients include a concentration of a marker dye that emits emission beams when illuminated with an excitation beam.

12. The instrument ofclaim 10, wherein the reaction ingredients include components for polymerase chain reaction.

13. The instrument ofclaim 1, wherein the plurality of vials comprises96 vials.

14. The instrument ofclaim 1, wherein the plurality of vials comprises a plastic unitary tray.

15. The instrument ofclaim 1, wherein the plurality of vials comprises96 vials in a plastic unitary tray.

16. A method comprising:

directing an excitation beam along an excitation beam path toward each of a plurality of vials, simultaneously;

splitting the excitation beam into light that is reflected and light that is passed;

directing light that is reflected from the beam splitter through a lens disposed along the excitation beam path between the light source and the plurality of vials, and simultaneously into each of the plurality of vials, to cause the plurality of vials to emit emission beams;

directing the emission beams from the plurality of vials through the beam splitter and to a detector; and

detecting the emission beams emitted from the plurality of vials.

17. The method ofclaim 16, wherein the wells contain different respective samples.

18. The method ofclaim 16, wherein the different respective samples each include a concentration of a marker dye that emits emission beams in response to being illuminated by the excitation beam, and wherein the method further includes generating primary data signals representative of the detected emission beams.

19. The method ofclaim 18, further comprising processing the primary data signals to compute corresponding concentrations of marker dye in the respective wells.

20. The method ofclaim 16, wherein the directing the emission beams from the plurality of vials through the beam splitter and to a detector, comprises directing the emission beams through a lens disposed along an emission beam path between the plurality of vials and the beam splitter.

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