Viral channel forming proteins - How to assemble and depolarize lipid membranes in silico

被引:4
|
作者
Fischer, Wolfgang B.
Kalita, Monoj Mon
Heermann, Dieter [1 ]
机构
[1] Heidelberg Univ, Inst Theoret Phys, Bergheimer Str 58, D-69115 Heidelberg, Germany
来源
关键词
Viral channel proteins; Protein structure; Protein assembly; Secondary structure prediction; Molecular dynamics simulations; Coarse grained simulations; INFLUENZA-A VIRUS; HEPATITIS-C VIRUS; M2 PROTON CHANNEL; MOLECULAR-DYNAMICS SIMULATIONS; FREE-ENERGY CALCULATIONS; HIV-1 VPU PROTEIN; SOLID-STATE NMR; HUMAN-PAPILLOMAVIRUS TYPE-16; ESCHERICHIA-COLI-CELLS; ION-CHANNEL;
D O I
10.1016/j.bbamem.2016.01.018
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Viral channel forming proteins (VCPs) have been discovered in the late 70s and are found in many viruses to date. Usually they are small and have to assemble to form channels which depolarize the lipid membrane of the host cells. Structural information is just about to emerge for just some of them. Thus, computational methods play a pivotal role in generating plausible structures which can be used in the drug development process. In this review the accumulation of structural data is introduced from a historical perspective. Computational performances and their predictive power are reported guided by biological questions such as the assembly, mechanism of function and drug-protein interaction of VCPs. An outlook of how coarse grained simulations can contribute to yet unexplored issues of these proteins is given. This article is part of a Special Issue entitled: Membrane Proteins edited by J.C. Gumbart and Sergei Noskov. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1710 / 1721
页数:12
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