Literature DB >> 25138674

Photobleaching reveals heterogeneous stoichiometry for equinatoxin II oligomers.

Matthew A B Baker1, Nejc Rojko, Bríd Cronin, Gregor Anderluh, Mark I Wallace.   

Abstract

Equinatoxin II (EqtII), a sea anemone cytolysin, is known to oligomerize to form pores that spontaneously insert into membranes. Crystallographic and cryo-EM studies of structurally similar cytolysins offer contradictory evidence for pore stoichiometry. Here we used single-molecule photobleaching of fluorescently labeled EqtII to determine the stoichiometry of EqtII oligomers in supported lipid bilayers. A frequency analysis of photobleaching steps revealed a log-normal distribution of stoichiometries with a mean of 3.4±2.3 standard deviations. Comparison of our experimental data with simulations of fixed stoichiometries supports our observation of a heterogeneous distribution of EqtII oligomerization. These data are consistent with a model of EqtII stoichiometry where pores are on average tetrameric, but with large variation in the number of subunits in individual pores.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  equinatoxin; fluorescence; membrane proteins; photobleaching; pore-forming toxins; single molecule fluorescence

Mesh:

Substances:

Year:  2014        PMID: 25138674     DOI: 10.1002/cbic.201300799

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  12 in total

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2.  Disrupting a key hydrophobic pair in the oligomerization interface of the actinoporins impairs their pore-forming activity.

Authors:  Haydeé Mesa-Galloso; Karelia H Delgado-Magnero; Sheila Cabezas; Aracelys López-Castilla; Jorge E Hernández-González; Lohans Pedrera; Carlos Alvarez; D Peter Tieleman; Ana J García-Sáez; Maria E Lanio; Uris Ros; Pedro A Valiente
Journal:  Protein Sci       Date:  2017-02-23       Impact factor: 6.725

3.  A pore-forming toxin requires a specific residue for its activity in membranes with particular physicochemical properties.

Authors:  Koldo Morante; Jose M M Caaveiro; Koji Tanaka; Juan Manuel González-Mañas; Kouhei Tsumoto
Journal:  J Biol Chem       Date:  2015-03-10       Impact factor: 5.157

4.  Toxicity of an α-pore-forming toxin depends on the assembly mechanism on the target membrane as revealed by single molecule imaging.

Authors:  Yamunadevi Subburaj; Uris Ros; Eduard Hermann; Rudi Tong; Ana J García-Sáez
Journal:  J Biol Chem       Date:  2014-12-18       Impact factor: 5.157

5.  Synergistic Action of Actinoporin Isoforms from the Same Sea Anemone Species Assembled into Functionally Active Heteropores.

Authors:  Esperanza Rivera-de-Torre; Sara García-Linares; Jorge Alegre-Cebollada; Javier Lacadena; José G Gavilanes; Álvaro Martínez-Del-Pozo
Journal:  J Biol Chem       Date:  2016-04-27       Impact factor: 5.157

Review 6.  Assembling the puzzle: Oligomerization of α-pore forming proteins in membranes.

Authors:  Katia Cosentino; Uris Ros; Ana J García-Sáez
Journal:  Biochim Biophys Acta       Date:  2015-09-12

7.  The effect of cholesterol on the long-range network of interactions established among sea anemone Sticholysin II residues at the water-membrane interface.

Authors:  Sara García-Linares; Ida Alm; Terhi Maula; José G Gavilanes; Johan Peter Slotte; Álvaro Martínez-Del-Pozo
Journal:  Mar Drugs       Date:  2015-03-25       Impact factor: 5.118

8.  Functional characterization of sticholysin I and W111C mutant reveals the sequence of the actinoporin's pore assembly.

Authors:  Valeria Antonini; Victor Pérez-Barzaga; Silvia Bampi; David Pentón; Diana Martínez; Mauro Dalla Serra; Mayra Tejuca
Journal:  PLoS One       Date:  2014-10-28       Impact factor: 3.240

9.  Pore-Forming Proteins from Cnidarians and Arachnids as Potential Biotechnological Tools.

Authors:  Esperanza Rivera-de-Torre; Juan Palacios-Ortega; José G Gavilanes; Álvaro Martínez-Del-Pozo; Sara García-Linares
Journal:  Toxins (Basel)       Date:  2019-06-25       Impact factor: 4.546

10.  Dissecting the mechanism of action of actinoporins. Role of the N-terminal amphipathic α-helix in membrane binding and pore activity of sticholysins I and II.

Authors:  Gustavo P B Carretero; Eduardo F Vicente; Eduardo M Cilli; Carlos M Alvarez; Håvard Jenssen; Shirley Schreier
Journal:  PLoS One       Date:  2018-08-30       Impact factor: 3.240

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