» Articles » PMID: 64260

Influence of Membrane Thickness and Ion Concentration on the Properties of the Gramicidin a Channel. Autocorrelation, Spectral Power Density, Relaxation and Single-channel Studies

Overview
Specialties Biochemistry
Biophysics
Date 1977 Jan 4
PMID 64260
Citations 72
Authors
Affiliations
Soon will be listed here.
Abstract

The properties of the gramicidin A channel in membranes made from a series of monoglycerides have been studied. In agreement with previous studies, the dissociation rate constant kD of the dimeric channel was found to increase strongly with increasing chain length of the monoglyceride, corresponding to a decrease of the mean life-time of the channel. The value of kD, however, was not strictly correlated with the membrane thickness, as seen from a comparison of membranes with different solvent content. Furthermore, the life-time of the channel increased with the concentration of the permeable ion. This effect was tentatively explained by an electrostatic stabilization of the channel. The single-channel conductance lambda was found to decrease with increasing membrane thickness d, if d was varied by increasing the chain length of the lipid. On the other hand, if d was changed by varying the solvent content of the membranes formed from one and the same lipid, lambda remained constant. These observations were explained by the assumption of local inhomogeneities in the membrane thickness. A striking difference between the lambda values obtained from autocorrelation analysis in the presence of many presence of many channels (lambda a) and those obtained from single-channel experiments (lambda sc) occurred with membranes from longer chain-length monoglycerides. This difference disappeared at low ion concentrations. Electrostatic interactions between channels in local clusters were proposed for an interpretation of these findings.

Citing Articles

Intrinsic Lipid Curvature and Bilayer Elasticity as Regulators of Channel Function: A Comparative Single-Molecule Study.

Ashrafuzzaman M, Koeppe 2nd R, Andersen O Int J Mol Sci. 2024; 25(5).

PMID: 38474005 PMC: 10931550. DOI: 10.3390/ijms25052758.


Screening for bilayer-active and likely cytotoxic molecules reveals bilayer-mediated regulation of cell function.

Peyear T, Andersen O J Gen Physiol. 2023; 155(4).

PMID: 36763053 PMC: 9948646. DOI: 10.1085/jgp.202213247.


Lipopolysaccharide Modulates Biological Activities of Human-β-Defensin Analogues but Not Non-Ribosomally Synthesized Peptides.

Krishnakumari V, Binny T, Adicherla H, Nagaraj R ACS Omega. 2020; 5(12):6366-6375.

PMID: 32258871 PMC: 7114172. DOI: 10.1021/acsomega.9b03770.


Molecular Mechanism for Gramicidin Dimerization and Dissociation in Bilayers of Different Thickness.

Sun D, Peyear T, Bennett W, Andersen O, Lightstone F, Ingolfsson H Biophys J. 2019; 117(10):1831-1844.

PMID: 31676135 PMC: 7018991. DOI: 10.1016/j.bpj.2019.09.044.


Quantitative Characterization of Protein-Lipid Interactions by Free Energy Simulation between Binary Bilayers.

Park S, Yeom M, Andersen O, Pastor R, Im W J Chem Theory Comput. 2019; 15(11):6491-6503.

PMID: 31560853 PMC: 7076909. DOI: 10.1021/acs.jctc.9b00815.