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Free Energy Landscapes of Membrane Transport Proteins

Technical Report ·
DOI:https://doi.org/10.2172/1483996· OSTI ID:1483996
 [1];  [1];  [1];  [2];  [1];  [1];  [2];  [2];  [3]
  1. Argonne National Lab. (ANL), Argonne, IL (United States)
  2. Univ. of Illinois at Urbana-Champaign, Urbana, IL (United States)
  3. Univ. of Chicago, Chicago, IL (United States)

Molecular dynamics (MD) is now a widespread tool for investigating biochemical and biomolecular systems, its prevalence, in no small part, being due to significant advances in computational hardware over the last few decades. Even non-experts can now routinely use MD for protein and nucleic acid structure refinement, studying conformational switching events, and investigating solvation effects due to ligand/drug binding. Nonetheless, the vast majority of simulations being done today utilize only rudimentary algorithmic approaches – so-called “brute force” MD – which only permit access to a small fraction of what the approach has to offer. This is largely because the core algorithm is simple, while advanced techniques can require everything from more sophisticated models and data structures to complicated on-the-fly analysis. A core goal of this early science project is to bring one such advanced MD approach into the broader arena of high-performance computing.In particular, the powerful method of constant-pH MD has long been a relegated to experienced users and specialized model systems. In this work we develop and implement a constant-pH MD algorithm in the NAMD simulation engine making it suitable for deployment on large-scale, next-generation supercomputers as well as ambitious, cutting-edge biological applications. We report,for the first time, constant-pH simulations of a membrane transport protein and use the results to analyze its free energy landscape for ion-selectivity.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
National Science Foundation (NSF); National Institutes of Health (NIH); USDOE
DOE Contract Number:
AC02-06CH11357
OSTI ID:
1483996
Report Number(s):
ANL/ALCF/ESP--17/11; 148042
Country of Publication:
United States
Language:
English

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