Visualizing Orientation and Topology of ER Membrane Proteins In Planta.

Autor: Schlößer M; INRES-Chemical Signalling, University of Bonn, Bonn, Germany., Ugalde JM; INRES-Chemical Signalling, University of Bonn, Bonn, Germany., Meyer AJ; INRES-Chemical Signalling, University of Bonn, Bonn, Germany. andreas.meyer@uni-bonn.de.
Jazyk: angličtina
Zdroj: Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2024; Vol. 2772, pp. 371-382.
DOI: 10.1007/978-1-0716-3710-4_28
Abstrakt: The orientation of membrane proteins within the lipid bilayer is key to understanding their molecular function. Similarly, the proper topology of multispanning membrane proteins is crucial for their function. Although bioinformatics tools can predict these parameters assessing the presence of hydrophobic protein domains sufficiently long to span the membrane and other structural features, the predictions from different algorithms are often inconsistent. Therefore, experimental analysis becomes mandatory. Redox-based topology analysis exploits the steep gradient in the glutathione redox potential (E GSH ) across the ER membrane of about 80 mV to visualize the orientation of ER membrane proteins by fusing the E GSH biosensor roGFP2 to either the N- or the C-termini of the investigated protein sequence. Transient expression of these fusion proteins in tobacco leaves allows direct visualization of orientation and topology of ER membrane proteins in planta. The protocol outlined here is based on either a simple merge of the two excitation channels of roGFP2 or a colocalization analysis of the two channels and thus avoids ratiometric analysis of roGFP2 fluorescence.
(© 2024. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.)
Databáze: MEDLINE
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