The geometry of diphtheria toxoid CRM197 channel assessed by thiazolium salts and nonelectrolytes-Reference-Cited by-同舟云学术

The geometry of diphtheria toxoid CRM197 channel assessed by thiazolium salts and nonelectrolytes

Published:2021-06 Issue:12 Volume:120 Page:2577-2591
ISSN:0006-3495
Container-title:Biophysical Journal
language:en
Short-container-title:Biophysical Journal

Author:

Shatursky Oleg Ya,Manoilov Kyrylo Yu,Gorbatiuk Oksana B.,Usenko Mariya O.,Zhukova Dariia A.,Vovk Andriy I.,Kobzar Oleksandr L.,Trikash Irene O.,Borisova Tatiana A.,Kolibo Denys V.,Komisarenko Serhiy V.

Publisher

Elsevier BV

Subject

Biophysics

Reference43 articles.

1. Channels formed by botulinum, tetanus, and diphtheria toxins in planar lipid bilayers: relevance to translocation of proteins across membranes;Hoch;Proc. Natl. Acad. Sci. USA,1985

2. The endosomal-lysosomal system: from acidification and cargo sorting to neurodegeneration;Hu;Transl. Neurodegener,2015

3. Mapping the membrane topography of the TH6-TH7 segment of the diphtheria toxin T-domain channel;Kienker;J. Gen. Physiol,2015

4. Structural basis for lack of toxicity of the diphtheria toxin mutant CRM197;Malito;Proc. Natl. Acad. Sci. USA,2012

5. Diphtheria toxin fragment forms large pores in phospholipid bilayer membranes;Kagan;Proc. Natl. Acad. Sci. USA,1981

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