Sharon Hammes-Schiffer

Last updated

Sharon Hammes-Schiffer
Born
Sharon Hammes-Schiffer

May 27, 1966 (1966-05-27) (age 57)
Nationality American
Alma mater Princeton University
Stanford
Known for Computational chemistry
Awards National Academy of Sciences (2013) Willard Gibbs Award (2021)
Scientific career
Fields Chemistry Biophysical Chemistry Physical Chemistry Materials Chemistry
Institutions Yale University
Website http://www.hammes-schiffer-group.org/

Sharon Hammes-Schiffer (born May 27, 1966) is a physical chemist who has contributed to theoretical and computational chemistry. She is currently a Sterling Professor of Chemistry at Yale University. [1] She has served as senior editor and deputy editor of the Journal of Physical Chemistry [2] and advisory editor for Theoretical Chemistry Accounts. [3] As of 1 January 2015 she is editor-in-chief of Chemical Reviews . [2]

Contents

Hammes-Schiffer studies "chemical reactions in solution, in proteins and at electrochemical interfaces, particularly the transfer of charged particles driving many chemical and biological processes." [4] Her research draws upon the areas of chemistry, physics, biology, and computer science and is significant for the fields of biochemistry, inorganic chemistry, physical chemistry and physical organic chemistry. A theoretician who works with computational models, Hammes-Schiffer blends classical molecular dynamics and quantum mechanics into theories that have direct relevance to a variety of experimental areas. In studying proton, electron and proton coupled electron transfer, Hammes-Schiffer has formulated a general theory of proton-coupled electron transfer reactions that explains the behavior of protons in energy conversion processes. [2] [5] [6] Her research has enhanced the understanding of hydrogen tunneling and protein motion in enzyme catalysis. [3] [7] Her research group has also developed a nuclear-electronic orbital approach that allows scientists to incorporate nuclear quantum effects into electronic structure calculations. [7] Her work has application to a variety of experimental results and has implications for areas such as protein engineering, drug design, [8] catalyst of solar cells, and enzymatic reactions. [4]

Early life and education

Hammes-Schiffer completed her B.A. in chemistry at Princeton University in 1988. She completed her Ph.D. in chemistry at Stanford University in 1993 after working with Hans C. Andersen. [9] [2] [3] She then worked with John C. Tully at AT&T Bell Laboratories as a postdoctoral research scientist. [3]

Career

Hammes-Schiffer held positions on the faculty at the University of Notre Dame as Clare Boothe Luce Assistant Professor of Chemistry and Biochemistry (1995-2000) and at Pennsylvania State University (2000-2012). [3] [10] In 2012 she joined the University of Illinois at Urbana-Champaign as Swanlund Professor of Chemistry, [8] where she remained until 2017. [11] Since then, she has led the Hammes-Schiffer Research Group at Yale University, where she was named John Gamble Kirkwood Professor of Chemistry in 2018, and Sterling Professor of Chemistry in 2021. [12] Starting January 2024, she will join the faculty at Princeton University. [13] Hammes-Schiffer is an author or co-author on nearly 200 papers, and has given more than 200 invited talks. [14]

Research

Hammes-Schiffer's work delves primarily into three separate areas of chemistry: Proton-coupled electron transfer (PCET), Enzymatic Processes, and the Nuclear-Electronic Orbital method. [15] A sect of this research engages in the study of the Kinetic isotope effect, a difference in the reaction rate of a chemical based on what isotope is present.

Proton-coupled electron transfer (PCET)

The application of her work in PCET has elucidated the nature of various chemical mechanisms and led to her temperature dependence model of PCET rates. [16] [17] One such process, Quinol Oxidation, studied the Kinetic isotope effect on Ubiquinol and Plastoquinol with regards to temperature, finding that the free energy of activation is greater for hydrogen than for deuterium, meaning the reaction is slower for hydrogen and therefore irreversible, if specific conditions are satisfied. [18] This finding has since been used by other investigators to reinforce the notion that reactions may or may not be unidirectional by influencing reaction rates with the kinetic isotope effect. [19] Additionally, her study of PCET in Iron Bi-imidazoline complexes has refined common comprehension of PCET, having proven her theory that electron transfer rate increases under the kinetic isotope effect as "the proton transfer distance increases and the electron transfer distance decreases." [20] These mechanisms have helped support the research of other PCET studies, with her main PCET paper, "Theoretical Studies of Proton-Coupled Electron Transfer Reactions", [16] having been cited over 90 times by papers ranging from studying protein motion to enzyme dynamics. [21]

Enzymatic processes

Hammes-Schiffer studies the effects of quantum tunnelling and hydrogen bonding on enzymatic reactions. Her work on Soybean Lipoxygenase-1 changed common perception of a previously proposed tunneling region diagram, [22] finding that the temperature dependence of KIEs are inversely proportional to each other and that active environmental dynamics leads to less of the KIE and promotes catalysis. [23] This finding should be applicable to any other enzymes which can transfer a proton due to the fact that there aren't as many enzymatic options for non-ionic transfer of a proton and therefore tunneling must be used throughout the process. [23]

Nuclear-electronic orbital method (NEO)

Hammes-Schiffer has also pioneered work in what she calls the Nuclear-electronic orbital method (NEO) which allows for a more accurate estimate of nuclear properties such as density, geometry, frequencies, electronic coupling, and nuclear motions. [24] As described in her paper, "Incorporation of Nuclear Quantum effects in electronic structure," Radial basis function kernel, a gaussian algorithm used to support vector machines, is applied to determine electronic and molecular orbitals. The NEO approach is specifically applicable in determining the exact mechanisms of hydrogen transfer reactions while accounting for other variables such as quantum tunneling and zero point energy. Hammes-Schiffer claims that the NEO approach is significantly advantageous over other methods that incorporate nuclear quantum effects because of the method's ability to calculate vibrational states, its avoidance of Born–Oppenheimer approximation and its apparent and inherent incorporation of quantum effects. [25]

In her study, published in September 2016, Hammes-Schiffer contributed towards discovering the effects of the active site of the magnesium ion in the Scissile Phosphate cofactor complex. She discovered that rather than the magnesium ion lying in the center of the complex, the ion lies in a separate site, termed the Hoogsteen Face, where it lowers the pKa of the complex in order to facilitate a deprotonation reaction necessary for a self-cleavage reaction. [26]

Honors and awards

Hammes-Schiffer is a Fellow of the American Physical Society (2010), the American Chemical Society (2011), the American Academy of Arts and Sciences (2012), the American Association for the Advancement of Science (2013), the National Academy of Sciences (2013), and the Biophysical Society (2015). [9] She was elected as a member of the International Academy of Quantum Molecular Science in 2014. [4] [6] [7]

Hammes-Schiffer has received a number of awards, including the following:

Related Research Articles

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An atom is a particle that consists of a nucleus of protons and neutrons surrounded by an electromagnetically-bound cloud of electrons. The atom is the basic particle of the chemical elements, and the chemical elements are distinguished from each other by the number of protons that are in their atoms. For example, any atom that contains 11 protons is sodium, and any atom that contains 29 protons is copper. The number of neutrons defines the isotope of the element.

<span class="mw-page-title-main">Hydrogen</span> Chemical element, symbol H and atomic number 1

Hydrogen is the chemical element with the symbol H and atomic number 1. Hydrogen is the lightest element. At standard conditions hydrogen is a gas of diatomic molecules having the formula H2. It is colorless, odorless, tasteless, non-toxic, and highly combustible. Hydrogen is the most abundant chemical substance in the universe, constituting roughly 75% of all normal matter. Stars such as the Sun are mainly composed of hydrogen in the plasma state. Most of the hydrogen on Earth exists in molecular forms such as water and organic compounds. For the most common isotope of hydrogen each atom has one proton, one electron, and no neutrons.

Tennessine is a synthetic chemical element with the symbol Ts and atomic number 117. It is the second-heaviest known element and the penultimate element of the 7th period of the periodic table.

In physical organic chemistry, a kinetic isotope effect (KIE) is the change in the reaction rate of a chemical reaction when one of the atoms in the reactants is replaced by one of its isotopes. Formally, it is the ratio of rate constants for the reactions involving the light (kL) and the heavy (kH) isotopically substituted reactants (isotopologues):

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References

  1. "Hammes-Schiffer named Sterling Professor of Chemistry". YaleNews. Yale University. October 26, 2021. Retrieved November 16, 2021.
  2. 1 2 3 4 "Sharon Hammes-Schiffer joins Chemical Reviews as new editor-in-chief". ACS Chemistry for Life. American Chemical Society. December 2, 2014.
  3. 1 2 3 4 5 6 "2005 Iota Sigma Pi Agnes Fay Morgan Research Award" (PDF). Iota Sigma Pi: National Honor Society for Women in Chemistry. Retrieved June 15, 2015.
  4. 1 2 3 "Sharon Hammes-Schiffer and So Hirata Elected Members of IAQMS". Chemistry at Illinois. University of Illinois at Urbana-Champaign. Retrieved June 15, 2015.
  5. Hammes-Schiffer, Sharon (December 21, 2009). "Theory of Proton-Coupled Electron Transfer in Energy Conversion Processes". Accounts of Chemical Research. 42 (12): 1881–1889. doi:10.1021/ar9001284. PMC   2841513 . PMID   19807148.
  6. 1 2 "Sharon Hammes-Schiffer Elected International Academy of Quantum Molecular Science Member". PNNL. Pacific Northwest National Laboratory. 2014. Retrieved June 15, 2015.
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  9. 1 2 "Sharon Hammes-Schiffer named the inaugural Kirkwood Professor of Chemistry". Hammes-Schiffer Research Group. Yale University. August 24, 2017. Retrieved February 15, 2018.
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  12. "The Hammes-Schiffer Research Group" . Retrieved November 20, 2021.
  13. "Board approves 16 faculty appointments". Inside Princeton. Retrieved July 12, 2023.
  14. Hammes-Schiffer, Sharon. "Curriculum Vitae" (PDF). University of Illinois at Urbana-Champaign. Retrieved June 15, 2015.
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  18. Ludlow, Michelle K.; Soudackov, Alexander V.; Hammes-Schiffer, Sharon (May 27, 2009). "Theoretical Analysis of the Unusual Temperature Dependence of the Kinetic Isotope Effect in Quinol Oxidation". Journal of the American Chemical Society. 131 (20): 7094–7102. doi:10.1021/ja9001184. ISSN   0002-7863. PMC   2710000 . PMID   19351186.
  19. Liu, Yi; Roth, Justine P. (January 8, 2016). "A Revised Mechanism for Human Cyclooxygenase-2". Journal of Biological Chemistry. 291 (2): 948–958. doi: 10.1074/jbc.M115.668038 . ISSN   0021-9258. PMC   4705412 . PMID   26565028.
  20. Iordanova, Nedialka; Decornez, Hélène; Hammes-Schiffer, Sharon (April 1, 2001). "Theoretical Study of Electron, Proton, and Proton-Coupled Electron Transfer in Iron Bi-imidazoline Complexes". Journal of the American Chemical Society. 123 (16): 3723–3733. doi:10.1021/ja0100524. ISSN   0002-7863. PMID   11457104.
  21. pubmeddev. "Cited In for PubMed (Select 11942823) - PubMed - NCBI". www.ncbi.nlm.nih.gov. Retrieved November 7, 2016.
  22. Jonsson, Thorlakur; Glickman, Michael H.; Sun, Shujun; Klinman, Judith P. (January 1, 1996). "Experimental Evidence for Extensive Tunneling of Hydrogen in the Lipoxygenase Reaction: Implications for Enzyme Catalysis". Journal of the American Chemical Society. 118 (42): 10319–10320. doi:10.1021/ja961827p. ISSN   0002-7863.
  23. 1 2 Knapp, Michael J.; Rickert, Keith; Klinman, Judith P. (April 1, 2002). "Temperature-Dependent Isotope Effects in Soybean Lipoxygenase-1: Correlating Hydrogen Tunneling with Protein Dynamics". Journal of the American Chemical Society. 124 (15): 3865–3874. doi:10.1021/ja012205t. ISSN   0002-7863. PMID   11942823.
  24. "Nuclear Electronic Orbital Method – Hammes-Schiffer Research Group". hammes-schiffer-group.org. Retrieved November 8, 2016.
  25. Webb, Simon P.; Iordanov, Tzvetelin; Hammes-Schiffer, Sharon (September 1, 2002). "Multiconfigurational nuclear-electronic orbital approach: Incorporation of nuclear quantum effects in electronic structure calculations". The Journal of Chemical Physics. 117 (9): 4106–4118. Bibcode:2002JChPh.117.4106W. doi:10.1063/1.1494980. ISSN   0021-9606. S2CID   32064618.
  26. Zhang, Sixue; Stevens, David R.; Goyal, Puja; Bingaman, Jamie L.; Bevilacqua, Philip C.; Hammes-Schiffer, Sharon (October 6, 2016). "Assessing the Potential Effects of Active Site Mg Ions in the Ribozyme–Cofactor Complex". The Journal of Physical Chemistry Letters. 7 (19): 3984–3988. doi:10.1021/acs.jpclett.6b01854. PMC   5117136 . PMID   27677922.
  27. "NSF logoFaculty Early Career Development (CAREER) Awards". National Science Foundation. Archived from the original on March 3, 2016. Retrieved June 15, 2015.
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Further reading