James Gumbart and Klaus Schulten.
Molecular dynamics studies of the archaeal translocon.
Biophysical Journal, 90:2356-2367, 2006.
(PMC: 1403164)
GUMB2006
The translocon is a protein-conducting channel conserved over all domains of
life that serves to translocate proteins across or into membranes. While this
channel has been well-studied for many years, the recent discovery of a high-
resolution crystal structure opens up new avenues of exploration. Taking
advantage of this, we performed molecular dynamics simulations of the
translocon in a fully-solvated lipid bilayer, examining the translocation
abilities of monomeric SecYE by forcing two helices comprised of
different amino acid sequences to cross the channel. The simulations
revealed that the
so-called `plug' of SecYE swings open during translocation, closing
thereafter. Likewise, it was established that the so-called `pore ring' region of
SecYE forms an elastic, yet tight seal around the translocating
oligopeptides. The closed state of the channel was found to block permeation
of all ions and water molecules; in the open state, ions were blocked. Our
results suggest that the SecYE monomer is capable of forming an
active channel.
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