He won the 1958 Chemistry Prize for determining theamino acid sequence ofinsulin and numerous other proteins, demonstrating in the process that each had a unique, definite structure; this was a foundational discovery for thecentral dogma of molecular biology.
At the newly constructedLaboratory of Molecular Biology in Cambridge, he developed and subsequently refined thefirst-ever DNA sequencing technique, which vastly expanded the number of feasible experiments in molecular biology and remains in widespread use today. The breakthrough earned him the 1980 Nobel Prize in Chemistry, which he shared withWalter Gilbert andPaul Berg.
He is one of only three people to have won multiple Nobel Prizes in the same category (the others beingJohn Bardeen in physics andKarl Barry Sharpless in chemistry),[5] and one of five persons withtwo Nobel Prizes.
Frederick Sanger was born on 13 August 1918 inRendcomb, a small village inGloucestershire, England, the second son of Frederick Sanger, ageneral practitioner, and his wife, Cicely Sanger (née Crewdson).[6] He was one of three children. His brother, Theodore, was only a year older, while his sister May (Mary) was five years younger.[7] His father had worked as an Anglican medical missionary in China but returned to England because of ill health. He was 40 in 1916 when he married Cicely, who was four years younger. Sanger's father converted toQuakerism soon after his two sons were born and brought up the children as Quakers. Sanger's mother was the daughter of an affluent cotton manufacturer and had a Quaker background, but was not a Quaker.[7]
When Sanger was around five years old the family moved to the small village ofTanworth-in-Arden in Warwickshire. The family was reasonably wealthy and employed a governess to teach the children. In 1927, at the age of nine, he was sent to theDowns School, a residential preparatory school run by Quakers nearMalvern. His brother Theo was a year ahead of him at the same school. In 1932, at the age of 14, he was sent to the recently establishedBryanston School in Dorset. This used theDalton system and had a more liberal regime which Sanger much preferred. At the school he liked his teachers and particularly enjoyed scientific subjects.[7] Able to complete hisSchool Certificate a year early, for which he was awarded seven credits, Sanger was able to spend most of his last year of school experimenting in the laboratory alongside his chemistry master, Geoffrey Ordish, who had originally studied at Cambridge University and been a researcher in theCavendish Laboratory. Working with Ordish made a refreshing change from sitting and studying books and awakened Sanger's desire to pursue a scientific career.[8] In 1935, prior to heading off to college, Sanger was sent toSchule Schloss Salem in southern Germany on an exchange program. The school placed a heavy emphasis on athletics, which caused Sanger to be much further ahead in the course material compared to the other students. He was shocked to learn that each day was started with readings from Hitler'sMein Kampf, followed by aSieg Heil salute.[9]
In 1936 Sanger went toSt John's College, Cambridge, to study natural sciences. His father had attended the same college. For Part I of hisTripos he took courses in physics, chemistry, biochemistry and mathematics but struggled with physics and mathematics. Many of the other students had studied more mathematics at school. In his second year he replaced physics with physiology. He took three years to obtain his Part I. For his Part II he studied biochemistry and obtained a 1st Class Honours. Biochemistry was a relatively new department founded byGowland Hopkins with enthusiastic lecturers who includedMalcolm Dixon,Joseph Needham andErnest Baldwin.[7]
Both his parents died from cancer during his first two years at Cambridge. His father was 60 and his mother was 58. As an undergraduate Sanger's beliefs were strongly influenced by his Quaker upbringing. He was a pacifist and a member of thePeace Pledge Union. It was through his involvement with theCambridge Scientists' Anti-War Group that he met his future wife, Joan Howe, who was studying economics atNewnham College. They courted while he was studying for his Part II exams and married after he had graduated in December 1940. Sanger, although brought up and influenced by his religious upbringing, later began to lose sight of his Quaker related ways. He began to see the world through a more scientific lens, and with the growth of his research and scientific development he slowly drifted farther from the faith he grew up with. He had nothing but respect for the religious and states he took two things from it, truth and respect for all life.[10] Under theMilitary Training Act 1939 he was provisionally registered as aconscientious objector, and again under theNational Service (Armed Forces) Act 1939, before being granted unconditional exemption from military service by a tribunal. In the meantime he undertook training in social relief work at the Quaker centre, Spicelands, Devon and served briefly as a hospital orderly.[7]
Sanger began studying for aPhD in October 1940 underN.W. "Bill" Pirie. His project was to investigate whether edible protein could be obtained from grass. After little more than a month Pirie left the department andAlbert Neuberger became his adviser.[7] Sanger changed his research project to study the metabolism oflysine[11] and a more practical problem concerning the nitrogen of potatoes.[12] His thesis had the title, "The metabolism of the amino acid lysine in the animal body". He was examined byCharles Harington andAlbert Charles Chibnall and awarded his doctorate in 1943.[7]
Neuberger moved to theNational Institute for Medical Research in London, but Sanger stayed in Cambridge and in 1943 joined the group ofCharles Chibnall, a protein chemist who had recently taken up the chair in the Department of Biochemistry.[13] Chibnall had already done some work on the amino acid composition of bovineinsulin[14] and suggested that Sanger look at the amino groups in the protein. Insulin could be purchased from thepharmacy chainBoots and was one of the very few proteins that were available in a pure form. Up to this time Sanger had been funding himself. In Chibnall's group he was initially supported by theMedical Research Council and then from 1944 until 1951 by aBeit Memorial Fellowship for Medical Research.[6]
Sanger's first triumph was to determine the completeamino acidsequence of the two polypeptide chains of bovine insulin, A and B, in 1952 and 1951, respectively.[15][16] Prior to this it was widely assumed that proteins were somewhat amorphous. In determining these sequences, Sanger proved thatproteins have a defined chemical composition.[7]
To get to this point, Sanger refined a partition chromatography method first developed byRichard Laurence Millington Synge andArcher John Porter Martin to determine the composition of amino acids in wool. Sanger used a chemical reagent1-fluoro-2,4-dinitrobenzene (now, also known asSanger's reagent, fluorodinitrobenzene, FDNB or DNFB), sourced frompoisonous gas research by Bernard Charles Saunders at the Chemistry Department at Cambridge University. Sanger's reagent proved effective at labelling the N-terminal amino group at one end of the polypeptide chain.[17] He then partially hydrolysed the insulin into short peptides, either with hydrochloric acid or using an enzyme such astrypsin. The mixture of peptides was fractionated in two dimensions on a sheet of filter paper, first byelectrophoresis in one dimension and then, perpendicular to that, bychromatography in the other. The different peptide fragments of insulin, detected withninhydrin, moved to different positions on the paper, creating a distinct pattern that Sanger called "fingerprints". The peptide from the N-terminus could be recognised by the yellow colour imparted by the FDNB label and the identity of the labelled amino acid at the end of the peptide determined by complete acid hydrolysis and discovering which dinitrophenyl-amino acid was there.[7]
By repeating this type of procedure Sanger was able to determine the sequences of the many peptides generated using different methods for the initial partial hydrolysis. These could then be assembled into the longersequences to deduce the complete structure of insulin. Finally, because the A and B chains are physiologically inactive without the three linkingdisulfide bonds (two interchain, one intrachain on A), Sanger and coworkers determined their assignments in 1955.[18][19] Sanger's principal conclusion was that the two polypeptide chains of the protein insulin had precise amino acid sequences and, by extension, that every protein had a unique sequence. It was this achievement that earned him his firstNobel prize in Chemistry in 1958.[20] This discovery was crucial to the latersequence hypothesis ofFrancis Crick for developing ideas of how DNA codes for proteins.[21]
From 1951 Sanger was a member of the external staff of theMedical Research Council[6] and when they opened theLaboratory of Molecular Biology in 1962, he moved from his laboratories in the Biochemistry Department of the university to the top floor of the new building. He became head of the Protein Chemistry division.[7]
Prior to his move, Sanger began exploring the possibility of sequencing RNA molecules and began developing methods for separating ribonucleotide fragments generated with specific nucleases. This work he did while trying to refine the sequencing techniques he had developed during his work on insulin.[21]
The key challenge in the work was finding a pure piece of RNA to sequence. In the course of the work he discovered in 1964, with Kjeld Marcker, theformylmethionine tRNA which initiates protein synthesis in bacteria.[22] He was beaten in the race to be the first to sequence atRNA molecule by a group led byRobert Holley fromCornell University, who published the sequence of the 77 ribonucleotides ofalanine tRNA fromSaccharomyces cerevisiae in 1965.[23] By 1967 Sanger's group had determined the nucleotide sequence of the5S ribosomal RNA fromEscherichia coli, a small RNA of 120 nucleotides.[24]
Sanger then turned to sequencing DNA, which would require an entirely different approach. He looked at different ways of usingDNA polymerase I fromE. coli to copy single-stranded DNA.[25] In 1975, together withAlan Coulson, he published a sequencing procedure using DNA polymerase with radiolabelled nucleotides that he called the "Plus and Minus" technique.[26][27] This involved two closely related methods that generated short oligonucleotides with defined 3' termini. These could be fractionated byelectrophoresis on apolyacrylamide gel and visualised usingautoradiography. The procedure could sequence up to 80 nucleotides in one go and was a big improvement on what had gone before, but was still very laborious. Nevertheless, his group were able to sequence most of the 5,386 nucleotides of the single-strandedbacteriophageφX174.[28] This was the first fully sequenced DNA-based genome. To their surprise they discovered that thecoding regions of some of the genes overlapped with one another.[2]
In 1977 Sanger and colleagues introduced the "dideoxy" chain-termination method for sequencing DNA molecules, also known as the "Sanger method".[27][29] This was a major breakthrough and allowed long stretches of DNA to be rapidly and accurately sequenced. It earned him his second Nobel prize in Chemistry in 1980, which he shared withWalter Gilbert andPaul Berg.[30] The new method was used by Sanger and colleagues to sequence human mitochondrial DNA (16,569 base pairs)[31] and bacteriophage λ (48,502 base pairs).[32] The dideoxy method was eventually used to sequence the entirehuman genome.[33]
Sanger married Margaret Joan Howe (not to be confused withMargaret Sanger, the American pioneer of birth control) in 1940. She died in 2012. They had three children—Robin, born in 1943, Peter born in 1946 and Sally Joan born in 1960.[6] He said that his wife had "contributed more to his work than anyone else by providing a peaceful and happy home."[43]
Sanger retired in 1983, aged 65, to his home, "Far Leys", inSwaffham Bulbeck outside Cambridge.[2]
In 1992, theWellcome Trust and the Medical Research Council founded the Sanger Centre (now theSanger Institute), named after him.[44] The institute is on theWellcome Trust Genome Campus nearHinxton, only a few miles from Sanger's home. He agreed to having the Centre named after him when asked byJohn Sulston, the founding director, but warned, "It had better be good."[44] It was opened by Sanger in person on 4 October 1993, with a staff of fewer than 50 people, and went on to take a leading role in thesequencing of the human genome.[44] The Institute had about 900 people in 2020 and is one of the world's largestgenomic research centres.
Sanger said he found no evidence for a God so he became an agnostic.[45] In an interview published in theTimes newspaper in 2000 Sanger is quoted as saying: "My father was a committed Quaker and I was brought up as a Quaker, and for them truth is very important. I drifted away from those beliefs – one is obviously looking for truth, but one needs some evidence for it. Even if I wanted to believe in God I would find it very difficult. I would need to see proof."[46]
He declined the offer of aknighthood, as he did not wish to be addressed as "Sir". He is quoted as saying, "A knighthood makes you different, doesn't it, and I don't want to be different." In 1986 he accepted admission to theOrder of Merit, which can have only 24 living members.[43][45][46]
In 2007 the BritishBiochemical Society was given a grant by theWellcome Trust to catalogue and preserve the 35 laboratory notebooks in which Sanger recorded his research from 1944 to 1983. In reporting this matter,Science noted that Sanger, "the most self-effacing person you could hope to meet", was spending his time gardening at hisCambridgeshire home.[47]
Sanger died in his sleep atAddenbrooke's Hospital inCambridge on 19 November 2013.[43][48] As noted in his obituary, he had described himself as "just a chap who messed about in a lab",[49] and "academically not brilliant".[50]
Sanger, F.; Tuppy, H. (1951a), "The amino-acid sequence in the phenylalanyl chain of insulin. 1. The identification of lower peptides from partial hydrolysates",Biochemical Journal,49 (4):463–481,doi:10.1042/bj0490463,PMC1197535,PMID14886310.
Sanger, F.; Tuppy, H. (1951b), "The amino-acid sequence in the phenylalanyl chain of insulin. 2. The investigation of peptides from enzymic hydrolysates",Biochemical Journal,49 (4):481–490,doi:10.1042/bj0490481,PMC1197536,PMID14886311.
Sanger, F.; Thompson, E.O.P. (1953a), "The amino-acid sequence in the glycyl chain of insulin. 1. The identification of lower peptides from partial hydrolysates",Biochemical Journal,53 (3):353–366,doi:10.1042/bj0530353,PMC1198157,PMID13032078.
Sanger, F.; Thompson, E.O.P. (1953b), "The amino-acid sequence in the glycyl chain of insulin. 2. The investigation of peptides from enzymic hydrolysates",Biochemical Journal,53 (3):366–374,doi:10.1042/bj0530366,PMC1198158,PMID13032079.
Milstein, C.; Sanger, F. (1961), "An amino acid sequence in the active centre of phosphoglucomutase",Biochemical Journal,79 (3):456–469,doi:10.1042/bj0790456,PMC1205670,PMID13771000.
Brownlee, G.G.; Sanger, F. (1967), "Nucleotide sequences from the low molecular weight ribosomal RNA ofEscherichia coli",Journal of Molecular Biology,23 (3):337–353,doi:10.1016/S0022-2836(67)80109-8,PMID4291728.
Brownlee, G.G.; Sanger, F.; Barrell, B.G. (1968), "The sequence of 5S ribosomal ribonucleic acid",Journal of Molecular Biology,34 (3):379–412,doi:10.1016/0022-2836(68)90168-X,PMID4938553.
Jeppesen, P.G.; Barrell, B.G.; Sanger, F.; Coulson, A.R. (1972), "Nucleotide sequences of two fragments from the coat-protein cistron of bacteriophage R17 ribonucleic acid",Biochemical Journal,128 (5):993–1006,doi:10.1042/bj1280993h,PMC1173988,PMID4566195.
Sanger, F.; Donelson, J.E.; Coulson, A.R.; Kössel, H.; Fischer, D. (1973), "Use of DNA Polymerase I Primed by a Synthetic Oligonucleotide to Determine a Nucleotide Sequence in Phage f1 DNA",Proceedings of the National Academy of Sciences USA,70 (4):1209–1213,Bibcode:1973PNAS...70.1209S,doi:10.1073/pnas.70.4.1209,PMC433459,PMID4577794.
Sanger, F.; Coulson, A.R. (1975), "A rapid method for determining sequences in DNA by primed synthesis with DNA polymerase",Journal of Molecular Biology,94 (3):441–448,doi:10.1016/0022-2836(75)90213-2,PMID1100841.
Sanger, F.; Coulson, A.R.; Barrell, B.G.; Smith, A.J.; Roe, B.A. (1980), "Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing",Journal of Molecular Biology,143 (2):161–178,doi:10.1016/0022-2836(80)90196-5,PMID6260957.
Anderson, S.; Bankier, A.T.; Barrell, B.G.; De Bruijn, M.H.; Coulson, A.R.; Drouin, J.; Eperon, I.C.; Nierlich, D.P.; Roe, B.A.; Sanger, F.; Schreier, P.H.; Smith, A.J.; Staden, R.; Young, I.G. (1981), "Sequence and organization of the human mitochondrial genome",Nature,290 (5806):457–465,Bibcode:1981Natur.290..457A,doi:10.1038/290457a0,PMID7219534,S2CID4355527.
Anderson, S.; De Bruijn, M.H.; Coulson, A.R.; Eperon, I.C.; Sanger, F.; Young, I.G. (1982), "Complete sequence of bovine mitochondrial DNA. Conserved features of the mammalian mitochondrial genome",Journal of Molecular Biology,156 (4):683–717,doi:10.1016/0022-2836(82)90137-1,PMID7120390.
^Marks, Lara."Sequencing proteins: Insulin".The path to DNA sequencing: The life and work of Fred Sanger. What is Biotechnology. Retrieved1 September 2015.
^abMarks, Lara."The path to sequencing nucleic acids".The path to DNA sequencing: The life and work of Fred Sanger. What is Biotechnology. Retrieved1 September 2015.
^"Summit Overview Photo".Awards Council member and Nobel Prize laureate Dr. Charles H. Townes presenting the American Academy of Achievement's Golden Plate Award to British biochemist Dr. Frederick Sanger, recipient of two Nobel Prizes in Chemistry, at the 2000 Summit in Hampton Court.
^"2016 Awardees".American Chemical Society, Division of the History of Chemistry. University of Illinois at Urbana-Champaign School of Chemical Sciences. 2016. Archived fromthe original on 6 May 2017. Retrieved14 June 2017.
^"Citation for Chemical Breakthrough Award"(PDF).American Chemical Society, Division of the History of Chemistry. University of Illinois at Urbana-Champaign School of Chemical Sciences. 2016. Archived fromthe original(PDF) on 6 May 2017. Retrieved14 June 2017.
^abc"Frederick Sanger, OM".The Telegraph. 20 November 2013.Archived from the original on 12 January 2022. Retrieved20 November 2013.
^abHargittai, István (April 1999). "Interview: Frederick Sanger".The Chemical Intelligencer.4 (2). New York: Springer-Verlag:6–11.. This interview, which took place on 16 September 1997, was republished inHargittai, István (2002). "Chapter 5: Frederick Sanger".Candid science II: conversations with famous biomedical scientists. London: Imperial College Press. pp. 73–83.ISBN978-1-86094-288-4.
^"Frederick Sanger: Unassuming British biochemist whose pivotal and far-reaching discoveries made him one of a handful of double Nobel prizewinners".The Times. London. 21 November 2013. p. 63.
Brownlee, George G. (2014).Fred Sanger, double Nobel laureate: a biography. Cambridge, UK: Cambridge University Press.ISBN978-1-107-08334-9. Chapters 4-6 contain the 1992 interview that the author conducted with Sanger.
Finch, John (2008),A Nobel Fellow on every floor: a history of the Medical Research Council Laboratory of Molecular Biology, Cambridge: Medical Research Council,ISBN978-1-84046-940-0.
