Simulation-based prediction of phosphatidylinositol 4,5-bisphosphate binding to an ion channel.

Abstract:

:Protein-lipid interactions regulate many membrane protein functions. Using a multiscale approach that combines coarse-grained and atomistic molecular dynamics simulations, we have predicted the binding site for the anionic phospholipid phosphatidylinositol 4,5-bisphosphate (PIP(2)) on the Kir2.2 inwardly rectifying (Kir) potassium channel. Comparison of the predicted binding site to that observed in the recent PIP(2)-bound crystal structure of Kir2.2 reveals good agreement between simulation and experiment. In addition to providing insight into the mechanism by which PIP(2) binds to Kir2.2, these results help to establish the validity of this multiscale simulation approach and its future application in the examination of novel membrane protein-lipid interactions in the increasing number of high-resolution membrane protein structures that are now available.

journal_name

Biochemistry

journal_title

Biochemistry

authors

Schmidt MR,Stansfeld PJ,Tucker SJ,Sansom MS

doi

10.1021/bi301350s

subject

Has Abstract

pub_date

2013-01-15 00:00:00

pages

279-81

issue

2

eissn

0006-2960

issn

1520-4995

journal_volume

52

pub_type

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