bi061013d_si_001.pdf (101.03 kB)
Download fileSimulations of a Protein Translocation Pore: SecY†
journal contribution
posted on 2006-10-31, 00:00 authored by Shozeb Haider, Benjamin A. Hall, Mark S. P. SansomSecY is the central channel protein of the SecYEβ translocon, the structure of which has been
determined by X-ray diffraction. Extended (15 ns) MD simulations of the isolated SecY protein in a
phospholipid bilayer have been performed to explore the relationship between protein flexibility and the
mechanisms of channel gating. In particular, principal components analysis of the simulation trajectory
has been used to probe the intrinsic flexibility of the isolated SecY protein in the absence of the γ-subunit
(SecE) clamp. Analysis and visualization of the principal eigenvectors support a “plug and clamshell”
model of SecY channel gating. The simulation results also indicate that hydrophobic gating at the central
pore ring prevents leakage of water and ions through the channel in the absence of a translocating peptide.