Multiple cytosolic components promote intra-Golgi protein transport. Resolution of a protein acting at a late stage, prior to membrane fusion
- PMID: 3003102
Multiple cytosolic components promote intra-Golgi protein transport. Resolution of a protein acting at a late stage, prior to membrane fusion
Abstract
Cytosolic components are required to produce the "primed donor" and to consume the "dilution-resistant" intermediates of the intercompartmental protein transport pathway as elucidated in a cell-free system (Balch, W. E., Glick, B. S., and Rothman, J. E. (1984) Cell 39, 525-536, and Wattenberg, B. W., Balch, W. E., and Rothman, J. E. (1986) J. Biol. Chem. 261, 2202-2207). Widely different levels of crude cytosol are required for each of these steps, suggesting that different cytosolic components might mediate each step. Here, we fractionate cytosol and demonstrate that there are multiple transport-active components. Furthermore, we report the development of stage-specific functional assays which reveal that a distinct soluble component is required in the consumption of the dilution-resistant intermediate. This component, of about 25 kilodaltons in its apparent native molecular mass, is derived from calf brain cytosol. While this component mediates the consumption of the dilution-resistant intermediate, it is inactive in the priming stage. This stage-specific component seems likely to be involved in the processing of transport vesicles after the attachment of those vesicles to the target membranes.
Similar articles
-
A novel prefusion complex formed during protein transport between Golgi cisternae in a cell-free system.J Biol Chem. 1986 Feb 15;261(5):2202-7. J Biol Chem. 1986. PMID: 3003101
-
Transport of the vesicular stomatitis glycoprotein to trans Golgi membranes in a cell-free system.J Biol Chem. 1987 Sep 15;262(26):12502-10. J Biol Chem. 1987. PMID: 3040752
-
Sequential intermediates in the pathway of intercompartmental transport in a cell-free system.Cell. 1984 Dec;39(3 Pt 2):525-36. doi: 10.1016/0092-8674(84)90459-8. Cell. 1984. PMID: 6096009
-
ATP-coupled transport of vesicular stomatitis virus G protein. Functional boundaries of secretory compartments.J Biol Chem. 1986 Nov 5;261(31):14690-6. J Biol Chem. 1986. PMID: 3021751
-
Analysis of protein transport through the Golgi in a reconstituted cell-free system.J Electron Microsc Tech. 1991 Feb;17(2):150-64. doi: 10.1002/jemt.1060170204. J Electron Microsc Tech. 1991. PMID: 1901603 Review.
Cited by
-
Reconstitution of transport of vesicular stomatitis virus G protein from the endoplasmic reticulum to the Golgi complex using a cell-free system.J Cell Biol. 1987 Mar;104(3):749-60. doi: 10.1083/jcb.104.3.749. J Cell Biol. 1987. PMID: 3029144 Free PMC article.
-
Peroxisome biogenesis: involvement of ARF and coatomer.J Cell Biol. 1998 Apr 20;141(2):373-83. doi: 10.1083/jcb.141.2.373. J Cell Biol. 1998. PMID: 9548716 Free PMC article.
-
A novel 115-kD peripheral membrane protein is required for intercisternal transport in the Golgi stack.J Cell Biol. 1992 Sep;118(5):1015-26. doi: 10.1083/jcb.118.5.1015. J Cell Biol. 1992. PMID: 1512287 Free PMC article.
-
Retrograde transport from the Golgi region to the endoplasmic reticulum is sensitive to GTP gamma S.J Cell Biol. 1992 Mar;116(6):1357-67. doi: 10.1083/jcb.116.6.1357. J Cell Biol. 1992. PMID: 1541633 Free PMC article.
-
Identification of a 25-kD protein from yeast cytosol that operates in a prefusion step of vesicular transport between compartments of the Golgi.J Cell Biol. 1990 Apr;110(4):947-54. doi: 10.1083/jcb.110.4.947. J Cell Biol. 1990. PMID: 2182655 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources