دورية أكاديمية

Protein-protein docking with dynamic residue protonation states.

التفاصيل البيبلوغرافية
العنوان: Protein-protein docking with dynamic residue protonation states.
المؤلفون: Krishna Praneeth Kilambi, Kavan Reddy, Jeffrey J Gray
المصدر: PLoS Computational Biology, Vol 10, Iss 12, p e1004018 (2014)
بيانات النشر: Public Library of Science (PLoS), 2014.
سنة النشر: 2014
المجموعة: LCC:Biology (General)
مصطلحات موضوعية: Biology (General), QH301-705.5
الوصف: Protein-protein interactions depend on a host of environmental factors. Local pH conditions influence the interactions through the protonation states of the ionizable residues that can change upon binding. In this work, we present a pH-sensitive docking approach, pHDock, that can sample side-chain protonation states of five ionizable residues (Asp, Glu, His, Tyr, Lys) on-the-fly during the docking simulation. pHDock produces successful local docking funnels in approximately half (79/161) the protein complexes, including 19 cases where standard RosettaDock fails. pHDock also performs better than the two control cases comprising docking at pH 7.0 or using fixed, predetermined protonation states. On average, the top-ranked pHDock structures have lower interface RMSDs and recover more native interface residue-residue contacts and hydrogen bonds compared to RosettaDock. Addition of backbone flexibility using a computationally-generated conformational ensemble further improves native contact and hydrogen bond recovery in the top-ranked structures. Although pHDock is designed to improve docking, it also successfully predicts a large pH-dependent binding affinity change in the Fc-FcRn complex, suggesting that it can be exploited to improve affinity predictions. The approaches in the study contribute to the goal of structural simulations of whole-cell protein-protein interactions including all the environmental factors, and they can be further expanded for pH-sensitive protein design.
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 1553-734X
1553-7358
Relation: http://europepmc.org/articles/PMC4263365?pdf=render; https://doaj.org/toc/1553-734X; https://doaj.org/toc/1553-7358
DOI: 10.1371/journal.pcbi.1004018
URL الوصول: https://doaj.org/article/61deba20561b42ac8d9902abba944b88
رقم الأكسشن: edsdoj.61deba20561b42ac8d9902abba944b88
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:1553734X
15537358
DOI:10.1371/journal.pcbi.1004018