Fast (microsecond) experiments and molecular dynamics simulation are finally working hand-in-hand to provide validated atomistic pictures of protein folding dynamics. Larger proteins and millisecond folders are around the corner, although empirical force fields need more improvement before mechanistic predictions become as reliable as average rate coefficients or native structures. It is time to extend this simulation experiment interplay to misfolding, aggregation and binding processes. The problem is that such processes are usually slow - seconds to days. In order to compare experiment and simulation directly during the next 4 years, when simulations will not reach far beyond the 1 ms regime yet, the solution is simple: create small and fast experimental model systems for misfolding, aggregation and binding. These are analogous to fast two-state and downhill folding studied during the last 10 years: certainly not all proteins fold that way, but much useful was learned from our ability to directly compare such model proteins with simulation. Here, we propose development of: 1) ?6-85 as a model system for sheet-containing misfolded traps (T denaturation and T-jumps) as well as excess helix-containing traps (P denaturation, P-jumps). The key is that all folding and misfolding events are completed in ~ 1 ms or faster. 2a) Fast-folding tethered proteins (WW and ?6-85) to facilitate the interplay between transient aggregation and folding. Oligomeric aggregates include chimeras with elements swapped among monomers, as well as less structured aggregates. Tethering allows high effective concentrations without going to high protein concentration (leading to uncontrollable aggregation), and also helps keep MD simulation by keeping reactants in close proximity. 2b) U1A-RNA binding to multiple sites on U1A protein will be a fast model system for binding at multiple sites. 3) For the next generation of misfolding/aggregation/binding research, we will develop a single molecule instrument capable of high throughput (106 molecules/day) and studying 2 or more molecules interacting without cross-linking them or confining them in a micelle. Five simulation groups have been brought on board (Schulten, Shaw, Cheung, Luthey-Schulten and Pande), and their students/postdocs are already working closely with mine so simulation can be developed in parallel with the experiments. The goal is to provide data in the few microsecond to few millisecond range, amenable to full atom simulation over the next 4 years, so misfolding/aggregation/binding processes can be studied at the atomistic level, but on systems small and fast enough for simulation to work. We build on our knowledge of ?6-85, WW domain and U1A, so much is known experimentally and computationally about the monomeric building blocks of our misfolding/aggregation/binding models.

Public Health Relevance

Supercomputers have gotten fast enough to fold small proteins on the machine based on first principles. It is critical that these calculations be validated by experiments, to make sure the structures and mechanisms that come out of the computer match the real world. The successes with small proteins are laudable, but many protein diseases involve binding of proteins, aggregation of proteins, or misfolding: oculopharyngeal dystrophy, which causes weakness of eyelids and swallowing difficulty in adults, is an example where our proposal studies a closely related protein-nucleic acid complex. The computing problem is that binding, folding and aggregation of proteins is often a very slow process, still far beyond the reach of current computers. We will develop new protein and nucleic acid model systems that misfold, aggregate and bind really fast (microseconds to at most a few milliseconds), so current computers can be used to study these processes in real time.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM093318-04
Application #
8578400
Study Section
Macromolecular Structure and Function B Study Section (MSFB)
Program Officer
Wehrle, Janna P
Project Start
2010-05-01
Project End
2017-04-30
Budget Start
2013-09-01
Budget End
2014-04-30
Support Year
4
Fiscal Year
2013
Total Cost
$305,541
Indirect Cost
$75,541
Name
University of Illinois Urbana-Champaign
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Dave, Kapil; Jäger, Marcus; Nguyen, Houbi et al. (2016) High-Resolution Mapping of the Folding Transition State of a WW Domain. J Mol Biol 428:1617-36
Guin, Drishti; Sye, Kori; Dave, Kapil et al. (2016) Dodine as a transparent protein denaturant for circular dichroism and infrared studies. Protein Sci 25:1061-8
Dave, Kapil; Davtyan, Aram; Papoian, Garegin A et al. (2016) Environmental Fluctuations and Stochastic Resonance in Protein Folding. Chemphyschem 17:1341-8
Gelman, Hannah; Wirth, Anna Jean; Gruebele, Martin (2016) ReAsH as a Quantitative Probe of In-Cell Protein Dynamics. Biochemistry 55:1968-76
Zhang, Yi; Schulten, Klaus; Gruebele, Martin et al. (2016) Disulfide Bridges: Bringing Together Frustrated Structure in a Bioactive Peptide. Biophys J 110:1744-52
Dave, Kapil; Gelman, Hannah; Thu, Chu Thi Hien et al. (2016) The Effect of Fluorescent Protein Tags on Phosphoglycerate Kinase Stability Is Nonadditive. J Phys Chem B 120:2878-85
Prigozhin, Maxim B; Chao, Shu-Han; Sukenik, Shahar et al. (2015) Mapping fast protein folding with multiple-site fluorescent probes. Proc Natl Acad Sci U S A 112:7966-71
Wirth, Anna Jean; Liu, Yanxin; Prigozhin, Maxim B et al. (2015) Comparing Fast Pressure Jump and Temperature Jump Protein Folding Experiments and Simulations. J Am Chem Soc 137:7152-9
Dave, Kapil; Gruebele, Martin (2015) Fast-folding proteins under stress. Cell Mol Life Sci 72:4273-85
Goodman, J S; Chao, S-H; Pogorelov, T V et al. (2014) Filling up the heme pocket stabilizes apomyoglobin and speeds up its folding. J Phys Chem B 118:6511-8

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