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Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast
We have used an in vitro assay that reconstitutes transport from the ER to the Golgi complex in yeast to identify a functional vesicular intermediate in transit to the Golgi apparatus. Permeabilized yeast cells, which serve as the donor in this assay, release a homogeneous population of vesicles tha...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1990
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2116157/ https://www.ncbi.nlm.nih.gov/pubmed/2195039 |
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collection | PubMed |
description | We have used an in vitro assay that reconstitutes transport from the ER to the Golgi complex in yeast to identify a functional vesicular intermediate in transit to the Golgi apparatus. Permeabilized yeast cells, which serve as the donor in this assay, release a homogeneous population of vesicles that are biochemically distinct from the donor ER fraction. The isolated vesicles, containing a post-ER/pre-Golgi form of the marker protein pro-alpha-factor, were able to bind to and fuse with exogenously added Golgi membranes. The ability to isolate fusion competent vesicles provides direct evidence that ER to Golgi membrane transport is mediated by a discrete population of vesicular carriers. |
format | Text |
id | pubmed-2116157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1990 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21161572008-05-01 Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast J Cell Biol Articles We have used an in vitro assay that reconstitutes transport from the ER to the Golgi complex in yeast to identify a functional vesicular intermediate in transit to the Golgi apparatus. Permeabilized yeast cells, which serve as the donor in this assay, release a homogeneous population of vesicles that are biochemically distinct from the donor ER fraction. The isolated vesicles, containing a post-ER/pre-Golgi form of the marker protein pro-alpha-factor, were able to bind to and fuse with exogenously added Golgi membranes. The ability to isolate fusion competent vesicles provides direct evidence that ER to Golgi membrane transport is mediated by a discrete population of vesicular carriers. The Rockefeller University Press 1990-07-01 /pmc/articles/PMC2116157/ /pubmed/2195039 Text en This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Articles Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast |
title | Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast |
title_full | Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast |
title_fullStr | Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast |
title_full_unstemmed | Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast |
title_short | Isolation of a functional vesicular intermediate that mediates ER to Golgi transport in yeast |
title_sort | isolation of a functional vesicular intermediate that mediates er to golgi transport in yeast |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2116157/ https://www.ncbi.nlm.nih.gov/pubmed/2195039 |