Literature DB >> 11306554

Stoichiometry and kinetics of transport vesicle fusion with Golgi membranes.

J Ostermann1.   

Abstract

The in vitro complementation assay established by Rothman and co-workers continues to be an important tool to study intra-Golgi transport. In this study, kinetic modeling is used to identify four main parameters that, together, explain the basic features of an assay that is a modification of the original assay. First, the assay signal depends on the ratio of Golgi membranes to transport intermediates in the assay. Secondly, an inactivation rate describes how the activity of transport intermediates decreases over time. Thirdly, the rate at which transport intermediates irreversibly bind to Golgi membranes is measured independently of membrane fusion, thus allowing a quantitative distinction between these two steps. Fourthly, a single rate constant describes the remaining reactions, which result in membrane fusion. This approach of kinetic modeling of experiments is generally applicable to other in vitro assays of cell biological phenomena, permitting quantitative interpretations and an increased resolution of the experiments.

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Year:  2001        PMID: 11306554      PMCID: PMC1083864          DOI: 10.1093/embo-reports/kve067

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   8.807


  10 in total

1.  GTP hydrolysis by arf-1 mediates sorting and concentration of Golgi resident enzymes into functional COP I vesicles.

Authors:  J Lanoix; J Ouwendijk; C C Lin; A Stark; H D Love; J Ostermann; T Nilsson
Journal:  EMBO J       Date:  1999-09-15       Impact factor: 11.598

2.  Vesicle fusion in protein transport through the Golgi in vitro does not involve long-lived prefusion intermediates. A reassessment of the kinetics of transport as measured by glycosylation.

Authors:  R R Hiebsch; B W Wattenberg
Journal:  Biochemistry       Date:  1992-07-07       Impact factor: 3.162

3.  Regulation of intra-Golgi membrane transport by calcium.

Authors:  A Porat; Z Elazar
Journal:  J Biol Chem       Date:  2000-09-22       Impact factor: 5.157

4.  Stepwise assembly of functionally active transport vesicles.

Authors:  J Ostermann; L Orci; K Tani; M Amherdt; M Ravazzola; Z Elazar; J E Rothman
Journal:  Cell       Date:  1993-12-03       Impact factor: 41.582

5.  Transport of vesicular stomatitis virus glycoprotein in a cell-free extract.

Authors:  E Fries; J E Rothman
Journal:  Proc Natl Acad Sci U S A       Date:  1980-07       Impact factor: 11.205

6.  Pre- and post-Golgi vacuoles operate in the transport of Semliki Forest virus membrane glycoproteins to the cell surface.

Authors:  J Saraste; E Kuismanen
Journal:  Cell       Date:  1984-09       Impact factor: 41.582

7.  Reconstitution of the transport of protein between successive compartments of the Golgi measured by the coupled incorporation of N-acetylglucosamine.

Authors:  W E Balch; W G Dunphy; W A Braell; J E Rothman
Journal:  Cell       Date:  1984-12       Impact factor: 41.582

8.  Characterization of trypsin-sensitive factor(s) required for endosome-endosome fusion.

Authors:  M I Colombo; S Gonzalo; P Weidman; P Stahl
Journal:  J Biol Chem       Date:  1991-12-05       Impact factor: 5.157

9.  ER/Golgi intermediates acquire Golgi enzymes by brefeldin A-sensitive retrograde transport in vitro.

Authors:  C C Lin; H D Love; J N Gushue; J J Bergeron; J Ostermann
Journal:  J Cell Biol       Date:  1999-12-27       Impact factor: 10.539

10.  Isolation of functional Golgi-derived vesicles with a possible role in retrograde transport.

Authors:  H D Love; C C Lin; C S Short; J Ostermann
Journal:  J Cell Biol       Date:  1998-02-09       Impact factor: 10.539

  10 in total
  1 in total

1.  In vitro fusion between Saccharomyces cerevisiae secretory vesicles and cytoplasmic-side-out plasma membrane vesicles.

Authors:  Lorena Arrastua; Eider San Sebastian; Ana F Quincoces; Claude Antony; Unai Ugalde
Journal:  Biochem J       Date:  2003-03-01       Impact factor: 3.857

  1 in total

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