Vesicle capture by membrane‐bound Munc13‐1 requires self‐assembly into discrete clusters-Reference-Cited by-同舟云学术

Vesicle capture by membrane‐bound Munc13‐1 requires self‐assembly into discrete clusters

Published:2021-07-24 Issue:17 Volume:595 Page:2185-2196
ISSN:0014-5793
Container-title:FEBS Letters
language:en
Short-container-title:FEBS Lett

Author:

Li Feng¹²,Kalyana Sundaram Ramalingam Venkat¹²^ORCID,Gatta Alberto T.¹²^ORCID,Coleman Jeff¹²,Ramakrishnan Sathish¹²,Krishnakumar Shyam S.¹²^ORCID,Pincet Frederic¹²³^ORCID,Rothman James E.¹²

Affiliation:

1. Department of Cell Biology School of Medicine Yale University New Haven CT USA

2. Nanobiology Institute Yale School of Medicine West Haven CT USA

3. Laboratoire de Physique de l’Ecole normale supérieure ENS Université PSL CNRS Sorbonne Université Université de Paris Paris France

Funder

National Institutes of Health

Publisher

Wiley

Subject

Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/1873-3468.14157

Reference40 articles.

1. A Half-Zippered SNARE Complex Represents a Functional Intermediate in Membrane Fusion

2. Kinetic barriers to SNAREpin assembly in the regulation of membrane docking/priming and fusion

3. Low energy cost for optimal speed and control of membrane fusion

4. A direct role for the Sec1/Munc18-family protein Vps33 as a template for SNARE assembly

5. Syntaxin opening by the MUN domain underlies the function of Munc13 in synaptic-vesicle priming

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