Author
Listed:
- Alex J. B. Kreutzberger
(University of Virginia
University of Virginia)
- Volker Kiessling
(University of Virginia
University of Virginia)
- Christopher Stroupe
(University of Virginia
University of Virginia)
- Binyong Liang
(University of Virginia
University of Virginia)
- Julia Preobraschenski
(Max Planck Institute for Biophysical Chemistry)
- Marcelo Ganzella
(Max Planck Institute for Biophysical Chemistry)
- Mark A. B. Kreutzberger
(University of Virginia)
- Robert Nakamoto
(University of Virginia
University of Virginia)
- Reinhard Jahn
(Max Planck Institute for Biophysical Chemistry)
- J. David Castle
(University of Virginia
University of Virginia)
- Lukas K. Tamm
(University of Virginia
University of Virginia)
Abstract
Regulated exocytosis of synaptic vesicles is substantially faster than of endocrine dense core vesicles despite similar molecular machineries. The reasons for this difference are unknown and could be due to different regulatory proteins, different spatial arrangements, different vesicle sizes, or other factors. To address these questions, we take a reconstitution approach and compare regulated SNARE-mediated fusion of purified synaptic and dense core chromaffin and insulin vesicles using a single vesicle-supported membrane fusion assay. In all cases, Munc18 and complexin are required to restrict fusion in the absence of calcium. Calcium triggers fusion of all docked vesicles. Munc13 (C1C2MUN domain) is required for synaptic and enhanced insulin vesicle fusion, but not for chromaffin vesicles, correlating inversely with the presence of CAPS protein on purified vesicles. Striking disparities in calcium-triggered fusion rates are observed, increasing with curvature with time constants 0.23 s (synaptic vesicles), 3.3 s (chromaffin vesicles), and 9.1 s (insulin vesicles) and correlating with rate differences in cells.
Suggested Citation
Alex J. B. Kreutzberger & Volker Kiessling & Christopher Stroupe & Binyong Liang & Julia Preobraschenski & Marcelo Ganzella & Mark A. B. Kreutzberger & Robert Nakamoto & Reinhard Jahn & J. David Castl, 2019.
"In vitro fusion of single synaptic and dense core vesicles reproduces key physiological properties,"
Nature Communications, Nature, vol. 10(1), pages 1-11, December.
Handle:
RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11873-8
DOI: 10.1038/s41467-019-11873-8
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-11873-8. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.