Abstract:
:Ion channel proteins control ionic flux across biological membranes through conformational changes in their transmembrane pores. An exponentially increasing number of channel structures captured in different conformational states are now being determined; however, these newly resolved structures are commonly classified as either open or closed based solely on the physical dimensions of their pore, and it is now known that more accurate annotation of their conductive state requires additional assessment of the effect of pore hydrophobicity. A narrow hydrophobic gate region may disfavor liquid-phase water, leading to local dewetting, which will form an energetic barrier to water and ion permeation without steric occlusion of the pore. Here we quantify the combined influence of radius and hydrophobicity on pore dewetting by applying molecular dynamics simulations and machine learning to nearly 200 ion channel structures. This allows us to propose a simple simulation-free heuristic model that rapidly and accurately predicts the presence of hydrophobic gates. This not only enables the functional annotation of new channel structures as soon as they are determined, but also may facilitate the design of novel nanopores controlled by hydrophobic gates.
journal_name
Proc Natl Acad Sci U S Aauthors
Rao S,Klesse G,Stansfeld PJ,Tucker SJ,Sansom MSPdoi
10.1073/pnas.1902702116subject
Has Abstractpub_date
2019-07-09 00:00:00pages
13989-13995issue
28eissn
0027-8424issn
1091-6490pii
1902702116journal_volume
116pub_type
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