KABELKA, Ivo, Vasil GEORGIEV, Lisa MARX, Peter PAJTINKA, Karl LOHNER, Georg PABST, Rumiana DIMOVA and Robert VÁCHA. Magainin 2 and PGLa in Bacterial Membrane Mimics III: Membrane Fusion and Disruption. Biophysical Journal. New York, USA: Cell Press, 2022, vol. 121, No 5, p. 852-861. ISSN 0006-3495. Available from: https://dx.doi.org/10.1016/j.bpj.2021.12.035.
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Basic information
Original name Magainin 2 and PGLa in Bacterial Membrane Mimics III: Membrane Fusion and Disruption.
Authors KABELKA, Ivo (203 Czech Republic, belonging to the institution), Vasil GEORGIEV, Lisa MARX, Peter PAJTINKA (703 Slovakia, belonging to the institution), Karl LOHNER, Georg PABST, Rumiana DIMOVA and Robert VÁCHA (203 Czech Republic, guarantor, belonging to the institution).
Edition Biophysical Journal, New York, USA, Cell Press, 2022, 0006-3495.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10610 Biophysics
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
WWW URL
Impact factor Impact factor: 3.400
RIV identification code RIV/00216224:14740/22:00125525
Organization unit Central European Institute of Technology
Doi http://dx.doi.org/10.1016/j.bpj.2021.12.035
UT WoS 000765012800016
Keywords in English Cell Membrane; Cryoelectron Microscopy; Lipid Bilayers; Magainins; Membrane Fusion
Tags CF CRYO, rivok
Tags International impact, Reviewed
Changed by Changed by: Mgr. Pavla Foltynová, Ph.D., učo 106624. Changed: 11/1/2023 15:57.
Abstract
We previously speculated that the synergistically enhanced antimicrobial activity of Magainin 2 and PGLa is related to membrane adhesion, fusion, and further membrane remodeling. Here we combined computer simulations with time-resolved in vitro fluorescence microscopy, cryoelectron microscopy, and small-angle X-ray scattering to interrogate such morphological and topological changes of vesicles at nanoscopic and microscopic length scales in real time. Coarse grained simulations revealed formation of an elongated and bent fusion zone between vesicles in the presence of equimolar peptide mixtures. Vesicle adhesion and fusion were observed to occur within a few seconds by cryoelectron microscopy and corroborated by small-angle X-ray scattering measurements. The latter experiments indicated continued and time-extended structural remodeling for individual peptides or chemically linked peptide heterodimers but with different kinetics. Fluorescence microscopy further captured peptide-dependent adhesion, fusion, and occasional bursting of giant unilamellar vesicles a few seconds after peptide addition. The synergistic interactions between the peptides shorten the time response of vesicles and enhance membrane fusogenic and disruption properties of the equimolar mixture compared with the individual peptides.
Links
GA20-20152S, research and development projectName: Proteinová přitažlivost a selektivita pro buněčné membrány
Investor: Czech Science Foundation
LL2007, research and development projectName: Peptidoví zabijáci bakterií (Acronym: PeptideKillers)
Investor: Ministry of Education, Youth and Sports of the CR
LM2015085, research and development projectName: CERIT Scientific Cloud (Acronym: CERIT-SC)
Investor: Ministry of Education, Youth and Sports of the CR, CERIT Scientific Cloud
LM2018127, research and development projectName: Česká infrastruktura pro integrativní strukturní biologii (Acronym: CIISB)
Investor: Ministry of Education, Youth and Sports of the CR
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