All submissions of the EM system will be redirected to Online Manuscript Submission System. Authors are requested to submit articles directly to Online Manuscript Submission System of respective journal.


Charged Protein-Lipid Interactions: Membrane Thickness

Author(s): Kein Falasca

The actions of integral and peripheral membrane proteins, as well as cell disrupting peptides, are known to be influenced by charged amino acids. Although atomistic molecular dynamics studies have shed light on the mechanics of charged protein group membrane binding and translocation, the impact of the complete range of membrane Physio-chemical characteristics and topologies has yet to be investigated. We investigated the movement of an Arginine (Arg) side chain analogue across saturated phosphatidylcholine (PC) bilayers with hydrocarbon tail lengths ranging from 10 to 18 carbons in this paper. With increased penetration into the hydrocarbon core, the free energy profiles all show steep climbs, with predictable shifts between bilayers of varying thickness, resulting in a barrier reduction from 26 kcal/mol for 18 carbons to 6 kcal/mol for 10 carbons.

Share this