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Leonard Lerman

From Wikipedia, the free encyclopedia
American scientist (1925–2012)
Leonard Lerman
Born
Leonard Solomon Lerman

(1925-06-27)June 27, 1925
Pittsburgh, Pennsylvania
DiedSeptember 19, 2012(2012-09-19) (aged 87)
Cambridge, Massachusetts[1]
Alma materCalifornia Institute of Technology
Known forCell cloning, human karyotype
Scientific career
FieldsGenetics
InstitutionsVanderbilt University Nashville;University of Colorado Health Sciences Center, Denver;SUNY Albany
Thesis Studies on the reaction of antibody with simple substances. The slow contraction of frog muscle. The hemodynamics of aortic occlusion. (1949@)
Doctoral advisorLinus Pauling
Doctoral studentsSidney Altman,Tom Maniatis

Leonard Solomon Lerman (June 27, 1925 – September 19, 2012) was an American scientist most noted for his work on DNA.[1]

Life and career

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Lerman was born and raised in Pittsburgh, the son of Freamah and Meyer Lerman, Jewish immigrants from Ukraine.[1] His father was a department store buyer. Lerman began attendingthe Carnegie Institute of Technology before graduating from high school and received his BS in five semesters.[1] As a graduate student withLinus Pauling at theCalifornia Institute of Technology, Lerman discovered thatantibodies have two binding sites. Later, perhaps his most important discovery was that certain molecules bind toDNA byintercalation.[2][3][4] This discovery has shaped much of science's understanding about how drugs andmutagens interact with DNA.

Later, during a sabbatical at theUniversity of Cambridge, Lerman had a chance to work with later Nobel prize winnersSydney Brenner andFrancis Crick.[5]

Lerman led a productive research program atVanderbilt University inNashville, theUniversity of Colorado Health Sciences Center inDenver andSUNY Albany, the State University of New York at Albany. Lerman's lab crew included at least one Nobel prize winner,Sidney Altman, and another,Tom Maniatis, who also became one of the leading molecular biologists of his time.

Lerman's last major effort, begun with Stuart Fischer atSUNY, was the invention ofdenaturing gradient gel electrophoresis (DGGE),[6][7][8] a technique used to separate DNA molecules. DGGE is widely used by scientists who wish to ascertain biodiversity in microbial communities.

Dr. Lerman was also a senior member of one of the firstbiotechnology companies, theGenetics Institute, co-founded by one of his students,Tom Maniatis.[5] Dr. Lerman was a member of theNational Academy of Sciences, USA.[5]

References

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  1. ^abcdKaufman, Leslie (30 September 2012)."Leonard Lerman, a Pioneer in DNA Study, Is Dead at 87".The New York Times.
  2. ^Lerman, L. S. (1961). "Structural considerations in the interactions of deoxyribonucleic acid and acridines".Journal of Molecular Biology.3:18–30.doi:10.1016/s0022-2836(61)80004-1.PMID 13761054.
  3. ^Luzzati, V.; Masson, F.; Lerman, L. S. (1961). "Interaction of DNA and proflavine: a small-angle x-ray scattering study".J. Mol. Biol.3 (5):634–639.doi:10.1016/s0022-2836(61)80026-0.PMID 14467543.
  4. ^Lerman, L. S. (1963)."The structure of the DNA-acridine complex".Proc. Natl. Acad. Sci. USA.49 (1):94–102.Bibcode:1963PNAS...49...94L.doi:10.1073/pnas.49.1.94.PMC 300634.PMID 13929834.
  5. ^abcLeonard Lerman, former senior lecturer at MIT, dies at 87. MIT News, September 28, 2012.
  6. ^Fischer, Stuart G.; Lerman, Leonard S. (January 1979). "Length-independent separation of DNA restriction fragments in two-dimensional gel electrophoresis".Cell.16 (1):191–200.doi:10.1016/0092-8674(79)90200-9.PMID 369706.S2CID 9369012.
  7. ^Fischer, S. G.; Lerman, L. S. (1980)."Separation of random fragments of DNA according to properties of their sequences".Proc. Natl. Acad. Sci. USA.77 (8):4420–4424.Bibcode:1980PNAS...77.4420F.doi:10.1073/pnas.77.8.4420.PMC 349855.PMID 6254023.
  8. ^Fischer, S. G.; Lerman, L. S. (1983)."DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: Correspondence with melting theory".Proc. Natl. Acad. Sci. USA.80 (6):1579–1583.Bibcode:1983PNAS...80.1579F.doi:10.1073/pnas.80.6.1579.PMC 393645.PMID 6220406.

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