Capturing spontaneous partitioning of peripheral proteins using a biphasic membrane-mimetic model

Mark J. Arcario, Y. Zenmei Ohkubo, Emad Tajkhorshid

Research output: Contribution to journalArticlepeer-review

31 Scopus citations


Membrane binding of peripheral proteins, mediated by specialized anchoring domains, is a crucial step for their biological function. Computational studies of membrane insertion, however, have proven challenging and largely inaccessible, due to the time scales required for the complete description of the process, mainly caused by the slow diffusion of the lipid molecules composing the membrane. Furthermore, in many cases, the nature of the membrane "anchor", i.e., the part of the protein that inserts into the membrane, is also unknown. Here, we address some of these issues by developing and employing a simplified representation of the membrane by a biphasic solvent model which we demonstrate can be used efficiently to capture and describe the process of hydrophobic insertion of membrane anchoring domains in all-atom molecular dynamics simulations. Applying the model, we have studied the insertion of the anchoring domain of a coagulation protein (the GLA domain of human protein C), starting from multiple initial configurations varying with regard to the initial orientation and height of the protein with respect to the membrane. In addition to efficiently and consistently identifying the "keel" region as the hydrophobic membrane anchor, within a few nanoseconds each configuration simulated showed a convergent height (2.20 ± 1.04 Å) and angle with respect to the interface normal (23.37 ± 12.48°). We demonstrate that the model can produce the same results as those obtained from a full representation of a membrane, in terms of both the depth of penetration and the orientation of the protein in the final membrane-bound form with an order of magnitude decrease in the required computational time compared to previous models, allowing for a more exhaustive search for the correct membrane-bound configuration.

Original languageEnglish
Pages (from-to)7029-7037
Number of pages9
JournalJournal of Physical Chemistry B
Issue number21
StatePublished - Jun 2 2011


Dive into the research topics of 'Capturing spontaneous partitioning of peripheral proteins using a biphasic membrane-mimetic model'. Together they form a unique fingerprint.

Cite this