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PMID: 9759482 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Transporters of nucleotide sugars, ATP, and nucleotide sulfate in the endoplasmic reticulum and Golgi apparatus.

Annual review of biochemistry ·Vol. 67 ·1998-00-00 ·Pages 49-69

Hirschberg CB, Robbins PW, Abeijon C

Abstract

The lumens of the endoplasmic reticulum and Golgi apparatus are the subcellular sites where glycosylation, sulfation, and phosphorylation of secretory and membrane-bound proteins, proteoglycans, and lipids occur. Nucleotide sugars, nucleotide sulfate, and ATP are substrates for these reactions. ATP is also used as an energy source in the lumen of the endoplasmic reticulum during protein folding and degradation. The above nucleotide derivatives and ATP must first be translocated across the membrane of the endoplasmic reticulum and/or Golgi apparatus before they can serve as substrates in the above lumenal reactions. Translocation of the above solutes is mediated for highly specific transporters, which are antiporters with the corresponding nucleoside monophosphates as shown by biochemical and genetic approaches. Mutants in mammals, yeast, and protozoa showed that a defect in a specific translocator activity results in selective impairments of the above posttranslational modifications, including loss of virulence of pathogenic protozoa. Several of these transporters have been purified and cloned. Experiments with yeast and mammalian cells demonstrate that these transporters play a regulatory role in the above reactions. Future studies will address the structure of the above proteins, how they are targeted to different organelles, their potential as drug targets, their role during development, and the possible occurrence of specific diseases.

MeSH Terms
Adenosine Triphosphate/metabolism Biological Transport Carbohydrate Metabolism Carrier Proteins/metabolism Endoplasmic Reticulum/metabolism Golgi Apparatus/metabolism Nucleotides/metabolism Phosphoadenosine Phosphosulfate/metabolism
Chemicals
Carrier Proteins Nucleotides Phosphoadenosine Phosphosulfate Adenosine Triphosphate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Hirschberg C B
Department of Molecular and Cell Biology, Boston University Goldman School of Dental Medicine, Massachusetts 02118-2392, USA.
Robbins P W
Abeijon C
Article Info
Journal
Annual review of biochemistry
Abbr.
Annu Rev Biochem
ISSN
0066-4154
Published
1998-00-00
Pages
49-69
Language
English
Region
United States
NLM ID
2985150R
Subset
IM
Grants
NIGMS NIH HHS · GM30365 · United States
NIGMS NIH HHS · GM34396 · United States
NIGMS NIH HHS · GM45188 · United States
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