Literature DB >> 3003101

A novel prefusion complex formed during protein transport between Golgi cisternae in a cell-free system.

B W Wattenberg, W E Balch, J E Rothman.   

Abstract

Examination of a cell-free reconstitution of intercompartmental transport through the Golgi apparatus has enabled detection of two intermediates in the pathway (Balch, W. E., Glick, B. S., and Rothman, J. E. (1984) Cell 39, 525-536). These intermediates are thought to represent stages in the budding and fusion reactions of transport vesicles mediating such a transport process. Here we describe a new transport intermediate that is interposed between the previously established primed donor formation and the N-ethylmaleimide (NEM)-resistant acceptor intermediates. Consumption of this intermediate requires much less cytosol than its formation, and thus it has been termed the "dilution-resistant" intermediate. The dilution-resistant intermediate only forms in the presence of donor and acceptor membranes, and its consumption is sensitive to NEM. The transition from this state to the later, NEM-resistant form of the prefusion complex requires ATP as well as cytosol and may represent a processing of transport vesicles to permit their fusion.

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Year:  1986        PMID: 3003101

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  18 in total

1.  Identification of a 25-kD protein from yeast cytosol that operates in a prefusion step of vesicular transport between compartments of the Golgi.

Authors:  B W Wattenberg; R R Hiebsch; L W LeCureux; M P White
Journal:  J Cell Biol       Date:  1990-04       Impact factor: 10.539

2.  Reconstitution of transport of vesicular stomatitis virus G protein from the endoplasmic reticulum to the Golgi complex using a cell-free system.

Authors:  W E Balch; K R Wagner; D S Keller
Journal:  J Cell Biol       Date:  1987-03       Impact factor: 10.539

3.  Human neutrophil annexin I promotes granule aggregation and modulates Ca(2+)-dependent membrane fusion.

Authors:  J W Francis; K J Balazovich; J E Smolen; D I Margolis; L A Boxer
Journal:  J Clin Invest       Date:  1992-08       Impact factor: 14.808

4.  Purification of an N-ethylmaleimide-sensitive protein catalyzing vesicular transport.

Authors:  M R Block; B S Glick; C A Wilcox; F T Wieland; J E Rothman
Journal:  Proc Natl Acad Sci U S A       Date:  1988-11       Impact factor: 11.205

5.  Yeast and mammals utilize similar cytosolic components to drive protein transport through the Golgi complex.

Authors:  W G Dunphy; S R Pfeffer; D O Clary; B W Wattenberg; B S Glick; J E Rothman
Journal:  Proc Natl Acad Sci U S A       Date:  1986-03       Impact factor: 11.205

6.  Transcytosis-associated protein (TAP)/p115 is a general fusion factor required for binding of vesicles to acceptor membranes.

Authors:  M Barroso; D S Nelson; E Sztul
Journal:  Proc Natl Acad Sci U S A       Date:  1995-01-17       Impact factor: 11.205

7.  Release of putative exocytic transport vesicles from perforated MDCK cells.

Authors:  M K Bennett; A Wandinger-Ness; K Simons
Journal:  EMBO J       Date:  1988-12-20       Impact factor: 11.598

8.  Resolution of regulated secretion into sequential MgATP-dependent and calcium-dependent stages mediated by distinct cytosolic proteins.

Authors:  J C Hay; T F Martin
Journal:  J Cell Biol       Date:  1992-10       Impact factor: 10.539

9.  Efficient transport of Semliki Forest virus glycoproteins through a Golgi complex morphologically altered by Uukuniemi virus glycoproteins.

Authors:  N Gahmberg; R F Pettersson; L Kääriäinen
Journal:  EMBO J       Date:  1986-12-01       Impact factor: 11.598

10.  A novel 115-kD peripheral membrane protein is required for intercisternal transport in the Golgi stack.

Authors:  M G Waters; D O Clary; J E Rothman
Journal:  J Cell Biol       Date:  1992-09       Impact factor: 10.539

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