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PMID: 3129425 Published · ppublish English Journal Article

Identification of the GTP-binding protein encoded by Gi3 complementary DNA.

The Journal of biological chemistry ·Vol. 263 ·No. 14 ·1988-05-15 ·Pages 6476-9

Goldsmith P, Rossiter K, Carter A, Simonds W, Unson CG, Vinitsky R, Spiegel AM

Abstract

Three closely related, but distinct, GTP-binding proteins (G-proteins) are encoded by cDNAs arbitrarily designated Gi1, Gi2, and Gi3. The in vitro translated products of mRNAs prepared from Gi1, Gi2, and Gi3 cDNAs migrate as 41-, 40-, and 41-kDa proteins, respectively, on sodium dodecyl sulfate-polyacrylamide gels. Antisera were raised against synthetic decapeptides corresponding to a divergent sequence (residues 159-168 for Gi1 and Gi3; 160-169 for Gi2) of the three cDNAs and tested on immunoblots for reactivity with three purified G-proteins, G41 and G40 from brain and G41 from HL-60 cells. LD antisera (Gi1 peptide) react only with brain G41. LE antisera (Gi2 peptide) react only with brain G40, and SQ antisera (Gi3 peptide) react exclusively with HL-60 G41. The results indicate that the 41-kDa G-protein purified from HL-60 cells differs from the purified brain 41-kDa protein and suggest that the HL-60 cell protein corresponds to that encoded by Gi3 cDNA.

MeSH Terms
Amino Acid Sequence Animals Brain/metabolism Cattle DNA/genetics GTP-Binding Proteins/genetics,isolation & purification Genes Immune Sera Macromolecular Substances Molecular Weight Protein Biosynthesis Rats Transcription, Genetic
Chemicals
Immune Sera Macromolecular Substances DNA GTP-Binding Proteins
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Goldsmith P
Metabolic Diseases Branch, National Institute of Diabetes, Digestive, and Kidney Diseases, Bethesda, Maryland 20892.
Rossiter K
Carter A
Simonds W
Unson C G
Vinitsky R
Spiegel A M
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
1988-05-15
Pages
6476-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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