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Discrimination of Native-like States of Membrane Proteins with Implicit Membrane-based Scoring Functions
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    Discrimination of Native-like States of Membrane Proteins with Implicit Membrane-based Scoring Functions
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    Department of Biochemistry and Molecular Biology, Michigan State University, East Lansing, Michigan, United States
    Department of Natural Resource and Environmental Management, Faculty of Applied Science and Engineering, Khon Kaen University, Nong Khai Campus, Nong Khai 43000, Thailand
    § Theoretical Molecular Science Laboratory, RIKEN, Wako-shi, Japan
    *Address: 603 Wilson Road, Room BCH 218, East Lansing, MI, 48824. Phone: +1 (517) 432-7439. Fax: +1 (517) 353-9334. E-mail: [email protected]
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    Journal of Chemical Theory and Computation

    Cite this: J. Chem. Theory Comput. 2017, 13, 6, 3049–3059
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    https://doi.org/10.1021/acs.jctc.7b00254
    Published May 5, 2017
    Copyright © 2017 American Chemical Society

    Abstract

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    A scoring protocol based on implicit membrane-based scoring functions and a new protocol for optimizing the positioning of proteins inside the membrane was evaluated for its capacity to discriminate native-like states from misfolded decoys. A decoy set previously established by the Baker lab (Proteins: Struct., Funct., Genet.2006, 62, 1010–1025) was used along with a second set that was generated to cover higher resolution models. The Implicit Membrane Model 1 (IMM1), IMM1 model with CHARMM 36 parameters (IMM1-p36), generalized Born with simple switching (GBSW), and heterogeneous dielectric generalized Born versions 2 (HDGBv2) and 3 (HDGBv3) were tested along with the new HDGB van der Waals (HDGBvdW) model that adds implicit van der Waals contributions to the solvation free energy. For comparison, scores were also calculated with the distance-scaled finite ideal-gas reference (DFIRE) scoring function. Z-scores for native state discrimination, energy vs root-mean-square deviation (RMSD) correlations, and the ability to select the most native-like structures as top-scoring decoys were evaluated to assess the performance of the scoring functions. Ranking of the decoys in the Baker set that were relatively far from the native state was challenging and dominated largely by packing interactions that were captured best by DFIRE with less benefit of the implicit membrane-based models. Accounting for the membrane environment was much more important in the second decoy set where especially the HDGB-based scoring functions performed very well in ranking decoys and providing significant correlations between scores and RMSD, which shows promise for improving membrane protein structure prediction and refinement applications. The new membrane structure scoring protocol was implemented in the MEMScore web server (http://feiglab.org/memscore).

    Copyright © 2017 American Chemical Society

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    Supporting Information

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    . The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.jctc.7b00254.

    • Tables S1–S8 with detailed analysis results including Z-scores, correlation coefficients, and top1 and top10 RMSD values separately for each protein and averaged over proteins for different scoring function components (PDF)

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    This article is cited by 5 publications.

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    Journal of Chemical Theory and Computation

    Cite this: J. Chem. Theory Comput. 2017, 13, 6, 3049–3059
    Click to copy citationCitation copied!
    https://doi.org/10.1021/acs.jctc.7b00254
    Published May 5, 2017
    Copyright © 2017 American Chemical Society

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