Larissa Socrier,Somayeh Ahadi,Mark Skamrahl,Daniel B Werz,Claudia Steinem
{"title":"Isomerization of PhotoGb3 in Phase-separated Pore-spanning Membranes alters Shiga toxin Organization.","authors":"Larissa Socrier,Somayeh Ahadi,Mark Skamrahl,Daniel B Werz,Claudia Steinem","doi":"10.1016/j.bpj.2025.07.011","DOIUrl":null,"url":null,"abstract":"The lateral organization of Shiga toxin bound to a lipid membrane is significantly influenced by the fatty acid geometry of its receptor glycolipid Gb3, which is crucial for the protein's internalization into the host cell. To control the lipid geometry, we used a photoisomerizable azobenzene derivative of Gb3 (photo-Gb3) that can be switched between a trans- and cis-configuration under light. We reconstituted this photo-Gb3 into liquid-disordered (ld)/liquid-ordered (lo) phase-separated pore-spanning membranes (PSMs), creating freestanding bilayer parts (f-PSMs) composed of an lo-phase surrounded by ld-phase on the pore rims (s-PSMs). Upon UV irradiation, we observed small, mobile, and transient ld-domains in the f-PSMs, indicating a trans-to-cis-isomerization of the photo-Gb3. The mean diffusion coefficient of the ld-domains was determined to be 0.014 ± 0.009 μm2/s, from which we estimated a membrane surface viscosity of 12-21∙10-8 Pa s m, indicative of a lo-phase. Before photoisomerization, Shiga toxin B (STxB) bound homogeneously to the lo-phase in the f-PSMs harboring the photo-Gb3. Upon trans-to-cis-isomerization of the photo-Gb3, ld-lakes were again formed, and the homogeneous protein distribution turned into dynamic STxB density fluctuations, which are discussed in the context of the entry process of Shiga toxin into the host cell.","PeriodicalId":8922,"journal":{"name":"Biophysical journal","volume":"84 1","pages":""},"PeriodicalIF":3.2000,"publicationDate":"2025-07-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biophysical journal","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.bpj.2025.07.011","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOPHYSICS","Score":null,"Total":0}
引用次数: 0
Abstract
The lateral organization of Shiga toxin bound to a lipid membrane is significantly influenced by the fatty acid geometry of its receptor glycolipid Gb3, which is crucial for the protein's internalization into the host cell. To control the lipid geometry, we used a photoisomerizable azobenzene derivative of Gb3 (photo-Gb3) that can be switched between a trans- and cis-configuration under light. We reconstituted this photo-Gb3 into liquid-disordered (ld)/liquid-ordered (lo) phase-separated pore-spanning membranes (PSMs), creating freestanding bilayer parts (f-PSMs) composed of an lo-phase surrounded by ld-phase on the pore rims (s-PSMs). Upon UV irradiation, we observed small, mobile, and transient ld-domains in the f-PSMs, indicating a trans-to-cis-isomerization of the photo-Gb3. The mean diffusion coefficient of the ld-domains was determined to be 0.014 ± 0.009 μm2/s, from which we estimated a membrane surface viscosity of 12-21∙10-8 Pa s m, indicative of a lo-phase. Before photoisomerization, Shiga toxin B (STxB) bound homogeneously to the lo-phase in the f-PSMs harboring the photo-Gb3. Upon trans-to-cis-isomerization of the photo-Gb3, ld-lakes were again formed, and the homogeneous protein distribution turned into dynamic STxB density fluctuations, which are discussed in the context of the entry process of Shiga toxin into the host cell.
期刊介绍:
BJ publishes original articles, letters, and perspectives on important problems in modern biophysics. The papers should be written so as to be of interest to a broad community of biophysicists. BJ welcomes experimental studies that employ quantitative physical approaches for the study of biological systems, including or spanning scales from molecule to whole organism. Experimental studies of a purely descriptive or phenomenological nature, with no theoretical or mechanistic underpinning, are not appropriate for publication in BJ. Theoretical studies should offer new insights into the understanding ofexperimental results or suggest new experimentally testable hypotheses. Articles reporting significant methodological or technological advances, which have potential to open new areas of biophysical investigation, are also suitable for publication in BJ. Papers describing improvements in accuracy or speed of existing methods or extra detail within methods described previously are not suitable for BJ.