» Articles » PMID: 23870264

Statistical Analysis of Peptide-induced Graded and All-or-none Fluxes in Giant Vesicles

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2013 Jul 23
PMID 23870264
Citations 17
Authors
Affiliations
Soon will be listed here.
Abstract

Antimicrobial, cytolytic, and cell-penetrating peptides induce pores or perturbations in phospholipid membranes that result in fluxes of dyes into or out of lipid vesicles. Here we examine the fluxes induced by four of these membrane-active peptides in giant unilamellar vesicles. The type of flux is determined from the modality of the distributions of vesicles as a function of their dye content using the statistical Hartigan dip test. Graded and all-or-none fluxes correspond to unimodal and bimodal distributions, respectively. To understand how these distributions arise, we perform Monte Carlo simulations of peptide-induced dye flux into vesicles using a very simple model. The modality of the distributions depends on the rate constants of pore opening and closing, and dye flux. If the rate constants of pore opening and closing are both much smaller than that of dye flux through the pore, all-or-none influx occurs. However, if one of them, especially the rate constant for pore opening, increases significantly relative to the flux rate constant, the process becomes graded. In the experiments, we find that the flux type is the same in giant and large vesicles, for all peptides except one. But this one exception indicates that the flux type cannot be used to unambiguously predict the mechanism of membrane permeabilization by the peptides.

Citing Articles

Story of Pore-Forming Proteins from Deadly Disease-Causing Agents to Modern Applications with Evolutionary Significance.

Gupta L, Molla J, Prabhu A Mol Biotechnol. 2023; 66(6):1327-1356.

PMID: 37294530 DOI: 10.1007/s12033-023-00776-1.


The Important Role of Membrane Fluidity on the Lytic Mechanism of the α-Pore-Forming Toxin Sticholysin I.

Pedrera L, Ros U, Fanani M, Lanio M, Epand R, Garcia-Saez A Toxins (Basel). 2023; 15(1).

PMID: 36668899 PMC: 9865829. DOI: 10.3390/toxins15010080.


Planar aggregation of the influenza viral fusion peptide alters membrane structure and hydration, promoting poration.

Rice A, Haldar S, Wang E, Blank P, Akimov S, Galimzyanov T Nat Commun. 2022; 13(1):7336.

PMID: 36470871 PMC: 9722698. DOI: 10.1038/s41467-022-34576-z.


Standardizing characterization of membrane active peptides with microfluidics.

Al Nahas K, Keyser U Biomicrofluidics. 2021; 15(4):041301.

PMID: 34257793 PMC: 8266397. DOI: 10.1063/5.0048906.


Attacins: A Promising Class of Insect Antimicrobial Peptides.

Buonocore F, Fausto A, Della Pelle G, Roncevic T, Gerdol M, Picchietti S Antibiotics (Basel). 2021; 10(2).

PMID: 33672685 PMC: 7924397. DOI: 10.3390/antibiotics10020212.


References
1.
Tamba Y, Yamazaki M . Magainin 2-induced pore formation in the lipid membranes depends on its concentration in the membrane interface. J Phys Chem B. 2009; 113(14):4846-52. DOI: 10.1021/jp8109622. View

2.
Kristanc L, Svetina S, Gomiscek G . Effects of the pore-forming agent nystatin on giant phospholipid vesicles. Biochim Biophys Acta. 2011; 1818(3):636-44. DOI: 10.1016/j.bbamem.2011.11.036. View

3.
Svetlovics J, Wheaten S, Almeida P . Phase separation and fluctuations in mixtures of a saturated and an unsaturated phospholipid. Biophys J. 2012; 102(11):2526-35. PMC: 3368148. DOI: 10.1016/j.bpj.2012.04.017. View

4.
Morales-Penningston N, Wu J, Farkas E, Goh S, Konyakhina T, Zheng J . GUV preparation and imaging: minimizing artifacts. Biochim Biophys Acta. 2010; 1798(7):1324-32. PMC: 2885611. DOI: 10.1016/j.bbamem.2010.03.011. View

5.
Yu Y, Vroman J, Bae S, Granick S . Vesicle budding induced by a pore-forming peptide. J Am Chem Soc. 2009; 132(1):195-201. DOI: 10.1021/ja9059014. View