TY - JOUR
T1 - The cellular membrane as a mediator for small molecule interaction with membrane proteins
AU - Mayne, Christopher G.
AU - Arcario, Mark J.
AU - Mahinthichaichan, Paween
AU - Baylon, Javier L.
AU - Vermaas, Josh V.
AU - Navidpour, Latifeh
AU - Wen, Po Chao
AU - Thangapandian, Sundarapandian
AU - Tajkhorshid, Emad
N1 - Funding Information:
This work was supported in part by the National Institutes of Health (Grants R01-GM101048 , R01-GM086749 , U54-GM087519 , and P41-GM104601 to E.T.) and XSEDE compute resources (grant TG-MCA06N060 to E.T.). M.J.A. acknowledges past support from the NSF GRF Program . J.V.V. acknowledges support from the Sandia National Laboratories Campus Executive Program, which is funded by the Laboratory Directed Research and Development (LDRD) Program . Sandia is a multi-program laboratory managed and operated by Sandia Corporation, a wholly owned subsidiary of Lockheed Martin Corporation, for the US Department of Energy's National Nuclear Security Administration under Contract No. DE-AC04-94AL85000 .
Publisher Copyright:
© 2016 Elsevier B.V.
PY - 2016/10/1
Y1 - 2016/10/1
N2 - The cellular membrane constitutes the first element that encounters a wide variety of molecular species to which a cell might be exposed. Hosting a large number of structurally and functionally diverse proteins associated with this key metabolic compartment, the membrane not only directly controls the traffic of various molecules in and out of the cell, it also participates in such diverse and important processes as signal transduction and chemical processing of incoming molecular species. In this article, we present a number of cases where details of interaction of small molecular species such as drugs with the membrane, which are often experimentally inaccessible, have been studied using advanced molecular simulation techniques. We have selected systems in which partitioning of the small molecule with the membrane constitutes a key step for its final biological function, often binding to and interacting with a protein associated with the membrane. These examples demonstrate that membrane partitioning is not only important for the overall distribution of drugs and other small molecules into different compartments of the body, it may also play a key role in determining the efficiency and the mode of interaction of the drug with its target protein. This article is part of a Special Issue entitled: Biosimulations edited by Ilpo Vattulainen and Tomasz Róg.
AB - The cellular membrane constitutes the first element that encounters a wide variety of molecular species to which a cell might be exposed. Hosting a large number of structurally and functionally diverse proteins associated with this key metabolic compartment, the membrane not only directly controls the traffic of various molecules in and out of the cell, it also participates in such diverse and important processes as signal transduction and chemical processing of incoming molecular species. In this article, we present a number of cases where details of interaction of small molecular species such as drugs with the membrane, which are often experimentally inaccessible, have been studied using advanced molecular simulation techniques. We have selected systems in which partitioning of the small molecule with the membrane constitutes a key step for its final biological function, often binding to and interacting with a protein associated with the membrane. These examples demonstrate that membrane partitioning is not only important for the overall distribution of drugs and other small molecules into different compartments of the body, it may also play a key role in determining the efficiency and the mode of interaction of the drug with its target protein. This article is part of a Special Issue entitled: Biosimulations edited by Ilpo Vattulainen and Tomasz Róg.
KW - Membrane
KW - Membrane proteins
KW - Molecular dynamics
KW - Small molecules
UR - http://www.scopus.com/inward/record.url?scp=84969504895&partnerID=8YFLogxK
U2 - 10.1016/j.bbamem.2016.04.016
DO - 10.1016/j.bbamem.2016.04.016
M3 - Article
C2 - 27163493
AN - SCOPUS:84969504895
SN - 0005-2736
VL - 1858
SP - 2290
EP - 2304
JO - Biochimica et Biophysica Acta - Biomembranes
JF - Biochimica et Biophysica Acta - Biomembranes
IS - 10
ER -