Jump to content

Frances Arnold

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Biochemlife (talk | contribs) at 09:50, 4 October 2018 (→‎Research: links). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Frances Arnold
Born
Frances Hamilton Arnold

(1956-07-25) July 25, 1956 (age 67)
Edgewood, Allegheny County, Pennsylvania
CitizenshipAmerican
Alma materPrinceton University (B.S. Mechanical and aerospace engineering, 1979), University of California, Berkeley (PhD Chemical engineering, 1985)
Known fordirected evolution of enzymes
AwardsGarvan–Olin Medal (2005)
FASEB Excellence in Science Award (2007)
Draper Prize (2011)
National Medal of Technology and Innovation (2013)
Raymond and Beverly Sackler Prize in Convergence Research (2017)
Millennium Technology Prize
NAE Member
NAS Member
FREng
Nobel Prize in Chemistry (2018)
Scientific career
FieldsChemical Engineering
InstitutionsCaltech
Doctoral advisorHarvey Warren Blanch
Notable studentsChristopher Voigt, Huimin Zhao

Frances Hamilton Arnold (born July 25, 1956) is an American chemical engineer and recipient of the 2018 Nobel Prize in Chemistry for pioneering the use of directed evolution to create enzymes (biochemical molecules - often proteins - that catalyze, or speed up, chemical reactions) with improved and/or novel functions.[1] The directed evolution strategy involves iterative rounds of randomly mutating proteins' genes and screening for proteins with improved functions and it has been used create useful biological systems, including enzymes, metabolic pathways, genetic regulatory circuits, and organisms. Arnold is especially interested in its applications in green energy production and environmentally-friendly chemical synthesis. Arnold earned a B.S. in Mechanical and Aerospace Engineering from Princeton University in 1979 and a Ph.D. in Chemical Engineering from the University of California, Berkeley where she also did postdoctoral work in biophysical chemistry. She moved to the California Institute of Technology (Caltech) in 1986 and is currently Caltech's Linus Pauling Professor of Chemical Engineering, Bioengineering, and Biochemistry. She continues to study directed evolution and its applications in science, medicine, chemicals and energy.

Early life and education

Arnold is the daughter of Josephine Inman (Routheau) and nuclear physicist William Howard Arnold, and the granddaughter of Lieutenant General William Howard Arnold.[2] She grew up in the suburbs of Pittsburgh, including Edgewood, Shadyside and Squirrel Hill, graduating from Allderdice High School in 1974.[3] As a high schooler, she hitchhiked to Washington, D.C. to protest the Vietnam War and lived on her own working as a cocktail waitress at a local jazz club and a cab driver.[4]

Arnold studied mechanical and aerospace engineering at Princeton University, graduating in 1979 and went on to earn a PhD in chemical engineering from the University of California, Berkeley in 1985.[5] Her thesis work, carried out in the lab of Harvey Blanch, investigated affinity chromatography techniques.[6] After graduating, she performed postdoctoral research at UC Berkeley and Caltech.[7]

Career

Arnold is a member of the Advisory Board of the DOE-funded Joint BioEnergy Institute and the Packard Fellowships in Science and Engineering, and she serves on the President's Advisory Council of the King Abdullah University of Science and Technology (KAUST). She is currently serving as a judge for The Queen Elizabeth Prize for Engineering. She worked with the National Academy of Science's Science & Entertainment Exchange to help Hollywood screenwriters accurately portray science topics.[8]

She is co-inventor on over 40 US patents.[9] She co-founded Gevo, Inc., a company to make fuels and chemicals from renewable resources in 2005 and Provivi, a company to develop crop protection technology, in 2013.[10]

Research

Arnold pioneered the use of directed evolution to design enzymes (molecules that catalyze, or speed up, chemical reactions) that perform novel functions and/or work more effectively or efficiently than natural enzymes.[1] In nature, evolution by natural selection can lead to proteins (including enzymes) well-suited to carry out biological tasks, but natural selection can only act on existing sequence variations (mutations) and typically occurs over long time periods.[11] Arnold speeds up the process by introducing mutations in the underlying sequences of proteins; she then tests these mutations’ effects. If a mutation improves the proteins’ function she can keep iterating the process to optimize it further. This strategy has broad implications because it can be used to design proteins for a wide variety of applications.[12] For example, she has used directed evolution to design enzymes that can be used to produce renewable fuels and pharmaceutical compounds with less harm to the environment.[1]

One advantage of directed evolution is that the mutations don't have to be completely random; instead they can be random enough to discover unexplored potential, but not so random as to be inefficient. The number of possible mutation combinations is astronomical, but instead of just randomly trying to test as many as possible, Arnold integrates her knowledge of biochemistry to narrow down the options, focusing on introducing mutations in areas of the protein that are likely to have the most positive effect on activity and avoiding areas in which mutations would likely be, at best, neutral and at worst, detrimental (such as disrupting proper protein folding).[1]

Arnold was the first person to apply directed evolution to the optimization of enzymes;[1] her seminal work, published in 1993, used the method to engineer a version of subtilisin E that was active in a highly unnatural environment, namely in the organic solvent DMF.[13] She carried out the work using four sequential rounds of mutagenesis of the enzyme's gene, expressed by bacteria, through error-prone PCR. After each round she screened the enzymes for their ability to hydrolyze the milk protein casein in the presence of DMF by growing the bacteria on agar plates containing casein and DMF. The bacteria secreted the enzyme and, if it were functional, it would hydrolyze the casein and produce a visible halo. She selected the bacteria that had the biggest halos and isolated their DNA for further rounds of mutagenesis.[1] Using this method, she designed an enzyme that had 256 times more activity in DMF than the original.[14]

Following her seminal work, Arnold has further developed her methods and applied them under different selection criteria in order to optimize enzymes for different functions. She showed that, whereas naturally evolved enzymes tend to function well at a narrow temperature range, enzymes could be produced using directed evolution that could function at both high and low temperatures.[1] In addition to improving the existing functions of natural enzymes, Arnold has designed enzymes that perform functions for which no previous specific enzyme existed, such as when she evolved cytochrome P450 to carry out cyclopropanation[15] and carbene and nitrene transfer reactions.[1][16]

In addition to evolving individual molecules, Arnold has used directed evolution to co-evolve enzymes in biosynthetic pathways, such as those involved in the production of carotenoids[17] and L-methionine[18] in Escherichia coli (which has the potential to be used as a whole-cell biocatalyst).[1] Arnold has applied these methods to biofuel production. For example, she evolved bacteria to produce the biofuel isobutanol; it can be produced in E. coli bacteria, but the production pathway requires the cofactor NADPH, whereas E. coli makes the cofactor NADH. To circumvent this problem, Arnold evolved the enzymes in the pathway to use NADH instead of NADPH, allowing for the production of isobutanol.[1][19]

Arnold has also used directed evolution to design highly specific and efficient enzymes that can be used as environmentally-friendly alternatives to some industrial chemical synthesis procedures.[1] She, and others using her methods, has engineered enzymes that can carry out synthesis reactions more quickly, with fewer by-products, and in some cases eliminating the need for hazardous heavy metals.[14]

Arnold also uses structure-guided protein recombination to combine parts of different proteins to form protein chimeras with unique functions. She developed computational methods, such as SCHEMA, to predict how the parts can be combined without disrupting their parental structure, so that the chimeras will fold properly, and then applies directed evolution to further mutate the chimeras to optimize their functions.[20][21]

At Caltech, Arnold runs a laboratory that continues to research green chemistry and alternative energy, including the development of highly active enzymes (cellulolytic and biosynthetic enzymes) and microorganisms to convert renewable biomass to fuels and chemicals.

Personal life

Arnold lives in La Cañada Flintridge, California. She was married to James E. Bailey and they had one son, James. She was later remarried to Andrew E. Lange and they had two sons, William and Joseph.[22][23] She was diagnosed with breast cancer in 2005 and is a breast cancer survivor.[24]

Honors and awards

Arnold's work has been recognized by many awards, including the 2018 Nobel Prize in Chemistry, the 2011 Draper Prize and a 2013 National Medal of Technology and Innovation. She was elected to the American Academy of Arts and Sciences in 2011 and has the rare honor of being elected to all three National Academies in the United States[25] - The National Academy of Sciences, The National Academy of Engineering, and the Institute of Medicine. Arnold is a Fellow of the American Association for the Advancement of Science, the American Academy of Arts and Sciences, the American Academy of Microbiology, the American Institute for Medical and Biological Engineering and an International Fellow of the Royal Academy of Engineering in the UK.[citation needed]

In 2016 she became the first woman to win the Millennium Technology Prize, which she won for pioneering directed evolution.[26] In 2017, Arnold was awarded the Raymond and Beverly Sackler Prize in Convergence Research by the National Academy of Sciences, which recognizes extraordinary contributions to convergence research.[27]

In 2018 she was awarded the Nobel Prize in Chemistry for her work in directed evolution, making her the fifth woman to receive the award in its 117 years of existence.[28] She received a one-half share of the award, with the other half jointly awarded to George Smith and Gregory Winter "for the phage display of peptides and antibodies."[1]

References

  1. ^ a b c d e f g h i j k l "The Nobel Prize in Chemistry 2018" (PDF). The Royal Swedish Academy of Sciences. Retrieved October 3, 2018.
  2. ^ https://www.nap.edu/read/24773/chapter/4
  3. ^ Guarino, Ben (October 3, 2018). "'Her work is incredible': Pittsburgh native Frances Arnold shares Nobel Prize in chemistry". Pittsburgh Post-Gazette.
  4. ^ Kharif, Olga (March 15, 2012). "Frances Arnold's Directed Evolution". Bloomberg Businessweek. Retrieved September 1, 2012.
  5. ^ "Frances H. Arnold". NAE Website. Retrieved October 3, 2018.
  6. ^ "A to G | Harvey W. Blanch". stage.cchem.berkeley.edu. Retrieved October 3, 2018.
  7. ^ "Interview with Frances H. Arnold — Design by Evolution :: ChemViews Magazine :: ChemistryViews". www.chemistryviews.org. Retrieved October 3, 2018.
  8. ^ "Frances Arnold's directed evolution". American Association for the Advancement of Science. Retrieved October 3, 2018.
  9. ^ "Frances H. Arnold". NAE Website. Retrieved October 3, 2018.
  10. ^ "Frances H. Arnold". NAE Website. Retrieved October 3, 2018.
  11. ^ Cirino, Patrick C.; Arnold, Frances H., "Exploring the Diversity of Heme Enzymes through Directed Evolution", Directed Molecular Evolution of Proteins, Wiley-VCH Verlag GmbH & Co. KGaA, pp. 215–243, ISBN 3527304231, retrieved October 3, 2018
  12. ^ "Scientific Background on the Nobel Prize in Chemistry 2018" (PDF). Royal Swedish Academy of Sciences. October 3, 2018.
  13. ^ Chen, K.; Arnold, F. H. (June 15, 1993). "Tuning the activity of an enzyme for unusual environments: sequential random mutagenesis of subtilisin E for catalysis in dimethylformamide". Proceedings of the National Academy of Sciences. 90 (12): 5618–5622. doi:10.1073/pnas.90.12.5618. ISSN 0027-8424.
  14. ^ a b Fernholm, Ann (October 3, 2018). "A (r)evolution in chemistry" (PDF). The Nobel Prize in Chemistry 2018: Popular Science Background.
  15. ^ Coelho, Pedro S.; Brustad, Eric M.; Kannan, Arvind; Arnold, Frances H. (January 18, 2013). "Olefin cyclopropanation via carbene transfer catalyzed by engineered cytochrome P450 enzymes". Science (New York, N.Y.). 339 (6117): 307–310. doi:10.1126/science.1231434. ISSN 1095-9203. PMID 23258409.
  16. ^ Prier, Christopher K.; Hyster, Todd K.; Farwell, Christopher C.; Huang, Audrey; Arnold, Frances H. (April 4, 2016). "Asymmetric Enzymatic Synthesis of Allylic Amines: A Sigmatropic Rearrangement Strategy". Angewandte Chemie (International Ed. in English). 55 (15): 4711–4715. doi:10.1002/anie.201601056. ISSN 1521-3773. PMC 4818679. PMID 26970325.{{cite journal}}: CS1 maint: PMC format (link)
  17. ^ Schmidt-Dannert, C.; Umeno, D.; Arnold, F. H. (July 1, 2000). "Molecular breeding of carotenoid biosynthetic pathways". Nature Biotechnology. 18 (7): 750–753. doi:10.1038/77319. ISSN 1087-0156. PMID 10888843.
  18. ^ May, O.; Nguyen, P. T.; Arnold, F. H. (March 1, 2000). "Inverting enantioselectivity by directed evolution of hydantoinase for improved production of L-methionine". Nature Biotechnology. 18 (3): 317–320. doi:10.1038/73773. ISSN 1087-0156. PMID 10700149.
  19. ^ Bastian, Sabine; Liu, Xiang; Meyerowitz, Joseph T.; Snow, Christopher D.; Chen, Mike M. Y.; Arnold, Frances H. (May 2011). "Engineered ketol-acid reductoisomerase and alcohol dehydrogenase enable anaerobic 2-methylpropan-1-ol production at theoretical yield in Escherichia coli". Metabolic Engineering. 13 (3): 345–352. doi:10.1016/j.ymben.2011.02.004. ISSN 1096-7184. PMID 21515217.
  20. ^ "Structure-guided protein recombination". The Frances H. Arnold Research Group. Retrieved October 3, 2018. {{cite web}}: Cite has empty unknown parameter: |dead-url= (help)
  21. ^ Meyer, Michelle M.; Hochrein, Lisa; Arnold, Frances H. (November 6, 2006). "Structure-guided SCHEMA recombination of distantly related β-lactamases". Protein Engineering, Design and Selection. 19 (12): 563–570. doi:10.1093/protein/gzl045. ISSN 1741-0134.
  22. ^ "Andrew E. Lange '80". Princeton Alumni Weekly. Retrieved October 3, 2018.
  23. ^ "Andrew Lange, Scholar of the Cosmos, Dies at 52". NYT. Retrieved October 3, 2018.
  24. ^ Hamilton, Walter (July 3, 2011). "Frances Arnold: Career path of a Caltech scientist". Los Angeles Times. Retrieved September 1, 2012.
  25. ^ "Caltech Professor Frances H. Arnold Elected to the National Academy of Sciences". Caltech. May 5, 2008.
  26. ^ "Evolutionary engineer Frances Arnold wins €1m tech prize - BBC News". Bbc.com. Retrieved May 25, 2016.
  27. ^ "2017 Raymond and Beverly Sackler Prize in Convergence Research". National Academy of Sciencces. Retrieved March 11, 2017.
  28. ^ "Nobel Prize In Chemistry Honors Work That Demonstrates 'The Power Of Evolution'". NPR.org. Retrieved October 4, 2018.
  29. ^ "50 engineering leaders become Fellows of the Royal Academy of Engineering". Retrieved September 21, 2018.
  30. ^ "Pioneer of "Directed Evolution" Wins Lifetime Achievement Award | Caltech". The California Institute of Technology. Retrieved August 31, 2017.
  31. ^ "Frances Arnold (Doctor of Science)". Dartmouth College. June 11, 2017. Retrieved June 11, 2017.
  32. ^ "Evolutionary engineer Francis Arnold wins €1m tech prize". May 25, 2016. Retrieved May 25, 2016.
  33. ^ "Doing the right things". ETH Zurich. November 21, 2015. Retrieved November 23, 2015.
  34. ^ "Spotlight | National Inventors Hall of Fame". Invent.org. November 21, 2013. Retrieved May 28, 2016.
  35. ^ a b "PRESS RELEASE: President Obama Honors Nation's Top Scientists and Innovators". whitehouse.gov. December 21, 2012. Retrieved May 25, 2016.
  36. ^ "Eni Award 2013 Edition". Eni. Retrieved October 3, 2018.
  37. ^ "Recipients of the Charles Stark Draper Prize for Engineering". nae.edu. National Academy of Engineering. Retrieved October 3, 2018.
  38. ^ "Frances H. Arnold, Enzyme Engineering Award for 2007". www.engconf.org. Retrieved June 21, 2018.
Wikimedia Commons has media related to Frances Arnold.
Scholia has an author profile for Frances Arnold.
Retrieved from "https://en.wikipedia.org/w/index.php?title=Frances_Arnold&oldid=862431252"