Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
21
|
pubmed:dateCreated |
1993-8-30
|
pubmed:abstractText |
As is the case with many other peptide hormones of the brain and gut, gastrin requires a carboxyl-terminal amide moiety for optimal biological activity. In the structure of progastrin, the carboxyl-terminal Phe of gastrin is followed by the sequence Gly93-Arg94-Arg95, which must be processed sequentially by an endoprotease, a carboxypeptidase, and an amidating enzyme to produce amidated bioactive gastrin. To examine the molecular determinants of peptide amidation in vivo, we mutated the wild-type Gly93 residue of progastrin to Ala93 and Ser93 and expressed the three progastrin DNAs in GH3 and MTC 6-23 endocrine cell lines. Although substantial quantities of amidated gastrin were seen in cells expressing wild-type progastrin, replacement of Gly93 with Ala93 completely abolished production of amidated gastrin when the cells were incubated in standard medium containing only L-alanine. In a similar fashion, cells expressing [Ser93]progastrin also demonstrated no production of amidated gastrin. When cells expressing [Ala93]- or [Ser93]progastrin were incubated in the presence of 1 mg/ml D-alanine or D-serine, respectively, a small but consistent amount of amidated gastrin production was detected (< 1% of wild type). These data lead us to conclude that the amidating enzyme has a rigid substrate specificity for a glycine-extended precursor. Furthermore, this in vivo substrate specificity confirms the importance of the pro-S-alpha-hydrogen of the carboxyl-terminal glycine for enzyme-substrate recognition.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Amides,
http://linkedlifedata.com/resource/pubmed/chemical/DNA,
http://linkedlifedata.com/resource/pubmed/chemical/Gastrins,
http://linkedlifedata.com/resource/pubmed/chemical/Mixed Function Oxygenases,
http://linkedlifedata.com/resource/pubmed/chemical/Multienzyme Complexes,
http://linkedlifedata.com/resource/pubmed/chemical/Protein Precursors,
http://linkedlifedata.com/resource/pubmed/chemical/big gastrin,
http://linkedlifedata.com/resource/pubmed/chemical/peptidylglycine monooxygenase
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
0021-9258
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
25
|
pubmed:volume |
268
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
15929-34
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:8340416-Amides,
pubmed-meshheading:8340416-Amino Acid Sequence,
pubmed-meshheading:8340416-Animals,
pubmed-meshheading:8340416-Cloning, Molecular,
pubmed-meshheading:8340416-DNA,
pubmed-meshheading:8340416-Gastrins,
pubmed-meshheading:8340416-Humans,
pubmed-meshheading:8340416-Mixed Function Oxygenases,
pubmed-meshheading:8340416-Molecular Sequence Data,
pubmed-meshheading:8340416-Multienzyme Complexes,
pubmed-meshheading:8340416-Mutation,
pubmed-meshheading:8340416-Protein Precursors,
pubmed-meshheading:8340416-Protein Processing, Post-Translational,
pubmed-meshheading:8340416-Rats,
pubmed-meshheading:8340416-Substrate Specificity,
pubmed-meshheading:8340416-Tumor Cells, Cultured
|
pubmed:year |
1993
|
pubmed:articleTitle |
Substrate specificity of the gastrin-amidating enzyme.
|
pubmed:affiliation |
Department of Pediatrics, University of Michigan Medical Center, Ann Arbor 48109-0800.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|