Vesicle Fusion Probability Is Determined by the Specific Interactions of Munc18 *
Journal of Biological Chemistry, ISSN: 0021-9258, Vol: 285, Issue: 49, Page: 38141-38148
2010
- 11Citations
- 33Captures
Metric Options: CountsSelecting the 1-year or 3-year option will change the metrics count to percentiles, illustrating how an article or review compares to other articles or reviews within the selected time period in the same journal. Selecting the 1-year option compares the metrics against other articles/reviews that were also published in the same calendar year. Selecting the 3-year option compares the metrics against other articles/reviews that were also published in the same calendar year plus the two years prior.
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations11
- Citation Indexes11
- 11
- CrossRef9
- Captures33
- Readers33
- 33
Article Description
Mammalian-regulated secretion is absolutely dependent on four evolutionarily conserved proteins: three SNARE proteins and munc18. Dissecting the functional outcomes of the spatially organized protein interactions between these factors has been difficult because of the close interrelationship between different binding modes. Here, we investigated the spatial distribution of single munc18 molecules at the plasma membrane of cells and the underlying interactions between syntaxin and munc18. Disruption of munc18 binding to the N-terminal peptide motif of syntaxin did not alter munc18 localization on the plasma membrane but had a pronounced influence on the behavior of secretory vesicles and their likelihood to undergo fusion. We therefore conclude that interaction with the syntaxin N-peptide can confer differential release probabilities to secretory vesicles and may contribute to the delineation of secretory vesicle pools.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0021925820606780; http://dx.doi.org/10.1074/jbc.m110.164038; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=78649674599&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/20801887; http://www.jbc.org/lookup/doi/10.1074/jbc.M110.164038; https://syndication.highwire.org/content/doi/10.1074/jbc.M110.164038; https://linkinghub.elsevier.com/retrieve/pii/S0021925820606780; https://dx.doi.org/10.1074/jbc.m110.164038; http://europepmc.org/abstract/med/20801887; http://europepmc.org/articles/PMC2992247; https://www.jbc.org/content/285/49/38141; http://www.jbc.org/article/S0021925820606780/abstract; http://www.jbc.org/article/S0021925820606780/fulltext; http://www.jbc.org/article/S0021925820606780/pdf; https://www.jbc.org/article/S0021-9258(20)60678-0/abstract; http://www.jbc.org/content/285/49/38141; http://www.jbc.org/cgi/doi/10.1074/jbc.M110.164038; http://www.jbc.org/content/285/49/38141.abstract; http://www.jbc.org/content/285/49/38141.full; http://www.jbc.org/content/285/49/38141.full.pdf
American Society for Biochemistry & Molecular Biology (ASBMB)
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