Literature DB >> 29186229

HyRes: a coarse-grained model for multi-scale enhanced sampling of disordered protein conformations.

Xiaorong Liu1, Jianhan Chen.   

Abstract

Efficient coarse-grained (CG) models can be coupled with atomistic force fields to accelerate the sampling of atomistic energy landscapes in the multi-scale enhanced sampling (MSES) framework. This approach may be particularly suitable for generating atomistic conformational ensembles of intrinsically disordered proteins (IDPs). While MSES is relatively robust to inherent CG artifacts, achieving optimal sampling efficiency requires CG modeling to generate the local and long-range fluctuations that are largely consistent with those at the atomistic level. Here, we describe a new hybrid resolution CG model (HyRes) for MSES simulations of disordered protein states, which is specifically designed to provide semi-quantitative secondary structure propensities together with a qualitative description of long-range nonspecific interactions. The HyRes model contains an atomistic description of the backbone with intermediate resolution side chains. The secondary structure propensities are tuned by adjusting the backbone hydrogen-bonding strength and the ϕ/ψ torsion profile. The sizes and covalent geometries of the side chains are parameterized to reproduce distributions derived from atomistic simulations. Lennard-Jones parameters for sidechain beads are assigned to reproduce statistical potentials derived from the protein structural database, and then globally parameterized with nonspecific electrostatic interactions to reproduce the free energy profiles of pair wise interactions and the key conformational properties of model peptides. Application of HyRes to MSES simulations of small IDPs suggests that it is capable of driving faster structural transitions at the atomistic level and increasing the convergence rate compared to the Cα-only Gō-like models previously utilized. With further optimization, we believe that the new CG model could greatly improve the efficiency of MSES simulations of the larger and more complex IDPs frequently involved in cellular signalling and regulation.

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Year:  2017        PMID: 29186229      PMCID: PMC5729119          DOI: 10.1039/c7cp06736d

Source DB:  PubMed          Journal:  Phys Chem Chem Phys        ISSN: 1463-9076            Impact factor:   3.676


  84 in total

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Authors:  Djurre H de Jong; Gurpreet Singh; W F Drew Bennett; Clement Arnarez; Tsjerk A Wassenaar; Lars V Schäfer; Xavier Periole; D Peter Tieleman; Siewert J Marrink
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4.  Spontaneous fibril formation by polyalanines; discontinuous molecular dynamics simulations.

Authors:  Hung D Nguyen; Carol K Hall
Journal:  J Am Chem Soc       Date:  2006-02-15       Impact factor: 15.419

Review 5.  Perspective on the Martini model.

Authors:  Siewert J Marrink; D Peter Tieleman
Journal:  Chem Soc Rev       Date:  2013-08-21       Impact factor: 54.564

6.  Long-range correlated dynamics in intrinsically disordered proteins.

Authors:  Giacomo Parigi; Nasrollah Rezaei-Ghaleh; Andrea Giachetti; Stefan Becker; Claudio Fernandez; Martin Blackledge; Christian Griesinger; Markus Zweckstetter; Claudio Luchinat
Journal:  J Am Chem Soc       Date:  2014-11-04       Impact factor: 15.419

7.  Packing, specificity, and mutability at the binding interface between the p160 coactivator and CREB-binding protein.

Authors:  Stephen J Demarest; Songpon Deechongkit; H Jane Dyson; Ronald M Evans; Peter E Wright
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8.  Length Dependent Helix-Coil Transition Kinetics of Nine Alanine-Based Peptides.

Authors:  Ting Wang; Yongjin Zhu; Zelleka Getahun; Deguo Du; Cheng-Yen Huang; William F Degrado; Feng Gai
Journal:  J Phys Chem B       Date:  2004-09-30       Impact factor: 2.991

9.  Improved side-chain torsion potentials for the Amber ff99SB protein force field.

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10.  The power of coarse graining in biomolecular simulations.

Authors:  Helgi I Ingólfsson; Cesar A Lopez; Jaakko J Uusitalo; Djurre H de Jong; Srinivasa M Gopal; Xavier Periole; Siewert J Marrink
Journal:  Wiley Interdiscip Rev Comput Mol Sci       Date:  2014-05
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Review 2.  Conformational Dynamics of Intrinsically Disordered Proteins Regulate Biomolecular Condensate Chemistry.

Authors:  Anton Abyzov; Martin Blackledge; Markus Zweckstetter
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3.  Accelerating atomistic simulations of proteins using multiscale enhanced sampling with independent tempering.

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Journal:  J Comput Chem       Date:  2020-12-10       Impact factor: 3.672

4.  Pseudo-Improper-Dihedral Model for Intrinsically Disordered Proteins.

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Journal:  J Chem Theory Comput       Date:  2020-06-12       Impact factor: 6.006

Review 5.  Advanced Sampling Methods for Multiscale Simulation of Disordered Proteins and Dynamic Interactions.

Authors:  Xiping Gong; Yumeng Zhang; Jianhan Chen
Journal:  Biomolecules       Date:  2021-09-28
  5 in total

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