Steven D. Schwartz
Professor of Chemistry and Biochemistry
and of Applied Mathematics

address:  Department of Chemistry and Biochemistry
               1306 East University Blvd
               University of Arizona
               Tucson, AZ 85721
office:      Old Chemistry 202
phone:     (520) 621-6363
email:      sschwartz@email.arizona.edu
               Google Scholar

 
RESEARCH SUMMARY

1. Theoretical and computational biochemistry
We work on identifying computationally atomic details of enzymatic catalysis.
The microscopic mechanism of enzyme catalysis remains a hotly debated topic.
We have proposed that in certain enzymes, motions in the body of the protein
are an integral part of the chemical mechanism.
This was controversial because these motions are much faster than the
turnover rate, but work by us and other groups have verified this effect.
There are 2 practical difficulties in computer simulations of enzymes:
the accessible simulation times are much shorter than biologically important timescales,
and the enzymatic reaction coordinate is unknown.
We use tools like Transition Path Sampling that can overcome these obstacles
and can provide unbiased estimates of atomic details of the mechanism.
Also, we work on incorporating these insights into methodologies of enzyme design.

Recent results include:
● I. Zoi, D. Antoniou and S.D. Schwartz: Incorporating fast protein dynamics into enzyme design:
   a proposed mutant aromatic amine dehydrogenase,
J. Phys. Chem. B 121, 7290 (2017)

● R. Harijan, I. Zoi, D. Antoniou, S.D. Schwartz and V.L. Schramm: Catalytic-site design for inverse
   heavy-enzyme isotope effects in human PNP,
  PNAS 114, 6456 (2017)

● M. Varga, M. Dzierlnga and S.D. Schwartz: Structurally linked dynamics in lactate dehydrogenases of
   evolutionarily distinct species,
Biochemistry 56, 2488 (2017)

● M. Dzierlenga and S.D. Schwartz: Targeting a rate-promoting vibration with an allosteric mediator
   in LDH,
J. Phys. Chem. Lett. 7, 2591 (2016)

● X. Pan and S.D. Schwartz, Conformational heterogeneity in the Michaelis complex of LDH:
    an analysis of vibrational spectroscopy using Markov and hidden Markov models,
  
J. Phys. Chem.  B 120, 6612 (2016)

● I. Zoi, D. Antoniou, V.L. Schramm, S.D. Schwartz et al., Modulating enzyme catalysis through
   mutations
designed to alter rapid protein dynamics, JACS 138, 3403 (2016)
● M. Varga and S.D. Schwartz, Enzymatic kinetic isotope effects from first principles path sampling
   calculations
, J. Chem. Th. Comp. 12, 2047 (2016)

● M. Dzierlenga and S.D. Schwartz, Another look at the mechanisms of hydride transfer enzymes
   with
quantum and classical transition path sampling, J. Phys. Chem. Lett. 6, 1177 (2015)

● X. Pan  and S.D. Schwartz, Free energy surface of the Michaelis complex of LDH: a network analysis
   of
microsecond simulations, J. Phys. Chem. B 119, 5430 (2015)
● I. Zoi, M. Motley, D. Antoniou, V.L. Schramm and S.D. Schwartz: Enzyme homologues have distinct
   reaction paths through their transition states,
J. Phys. Chem. B 119, 3662 (2015)

S.D. Schwartz and V. Schramm, Enzymatic transition states and dynamic motion in barrier crossing,
    Nature Chem. Biol. 5, 551 (2009)

2. Mechanisms of genetic cardiac disease
We work on computational studies of point mutations in cardiac thin filament. Calcium binding and dissociation
within the cardiac thin filament is a fundamental regulator of normal contraction and relaxation.
Mutations that disrupt this allosterically mediated process have long been implicated in cardiomyopathy,
but atomic details of the mechanism remain elusive, preventing the design of new targeted therapies.
We built the first computer model of the thin filament of cardiac muscle and our simulations pinpointed how
mutations in one protein of a complex indirectly affect a second protein via structural and dynamic changes
in a third protein,resulting in a pathogenic change in thin filament function.
This atom-level insight is potentially highly actionable in drug design.
● M. McConnell, M. Williams, M. Lynn, B. Schwartz, S.D. Schwartz and J. Tardiff:
   Clinically divergent mutation effects on the structure and function of the
   human cardiac tropomyosin overlap, Biochemistry 56, 3403 (2017)

M. Williams, S. Lehman, J. Tardiff and S.D. Schwartz, Atomic resolution probe for allostery In the
  regulatory thin filament, PNAS 113, 3257 (2016)

3. Micelle formation
Development of novel surfactants is a topic of urgent studies because currently available surfactants have
deleterious environmental side-effects.
We study the formation and dynamics of micelles created from ramnolipids.
● R. Eismin, E. Munusamy, L. Kegel, D. Hogan, S.D. Schwartz and J. Pemberton: Evolution of  aggregate
   structure in solutions of anionic monorhamnolipids: experimental and computational results,
  
Langmuir 33, 7412 (2017)
● E. Munusamy, C. Luft, J. Pemberton and S.D. Schwartz: Structural properties of nonionic
   monorhamnolipid aggregates in water studied by classical molecular dynamics simulations,
  J. Phys. Chem. B 121, 5781 (2017)