RGSZ1, a G(z)-selective rgs protein in brain

Structure, membrane association, regulation by Gα(z) phosphorylation, and relationship to a G(z) gtpase-activating protein subfamily

Jun Wang, Axel Ducret, Yaping Tu, Tohru Kozasa, Ruedi Aebersold, Elliott M. Ross

Research output: Contribution to journalArticle

126 Citations (Scopus)

Abstract

We cloned the cDNA for human RGSZ1, the major G(z)-selective GTPase- activating protein (GAP) in brain (Wang, J., Tu, Y., Woodson, J., Song, X., and Ross, E. M. (1997) J. Biol. Chem. 272, 5732-5740) and a member of the RGS family of G protein GAPs. Its sequence is 83% identical to RET-RGS1 (except its N-terminal extension) and 56% identical to GAIP. Purified, recombinant RGSZ1, RET-RGS1, and GAIP each accelerated the hydrolysis of Gα(z)-GTP over 400-fold with K(m) values of ~2 nM. RGSZ1 was 100-fold selective for Gα(z) over Gα1, unusually specific among RGS proteins. Other enzymological properties of RGSZ1, brain G(z) GAP, and RET-RGS1 were identical; GAIP differed only in Mg2+ dependence and in its slightly lower selectivity for Gα(z). RGSZ1, RET-RGS1, and GAIP thus define a subfamily of G(z) GAPs within the RGS proteins. RGSZ1 has no obvious membrane-spanning region but is tightly membrane-bound in brain. Its regulatory activity in membranes depends on stable bilayer association. When co-reconstituted into phospholipid vesicles with G(z) and m2 muscarinic receptors, RGSZ1 increased agonist- stimulated GTPase >15-fold with EC50

Original languageEnglish
Pages (from-to)26014-26025
Number of pages12
JournalJournal of Biological Chemistry
Volume273
Issue number40
DOIs
StatePublished - Oct 2 1998
Externally publishedYes

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GTPase-Activating Proteins
Membrane structures
Phosphorylation
RGS Proteins
Brain
Association reactions
Membranes
Muscarinic M2 Receptors
Proteins
GTP Phosphohydrolases
Guanosine Triphosphate
GTP-Binding Proteins
Hydrolysis
Phospholipids
Complementary DNA

All Science Journal Classification (ASJC) codes

  • Biochemistry

Cite this

RGSZ1, a G(z)-selective rgs protein in brain : Structure, membrane association, regulation by Gα(z) phosphorylation, and relationship to a G(z) gtpase-activating protein subfamily. / Wang, Jun; Ducret, Axel; Tu, Yaping; Kozasa, Tohru; Aebersold, Ruedi; Ross, Elliott M.

In: Journal of Biological Chemistry, Vol. 273, No. 40, 02.10.1998, p. 26014-26025.

Research output: Contribution to journalArticle

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abstract = "We cloned the cDNA for human RGSZ1, the major G(z)-selective GTPase- activating protein (GAP) in brain (Wang, J., Tu, Y., Woodson, J., Song, X., and Ross, E. M. (1997) J. Biol. Chem. 272, 5732-5740) and a member of the RGS family of G protein GAPs. Its sequence is 83{\%} identical to RET-RGS1 (except its N-terminal extension) and 56{\%} identical to GAIP. Purified, recombinant RGSZ1, RET-RGS1, and GAIP each accelerated the hydrolysis of Gα(z)-GTP over 400-fold with K(m) values of ~2 nM. RGSZ1 was 100-fold selective for Gα(z) over Gα1, unusually specific among RGS proteins. Other enzymological properties of RGSZ1, brain G(z) GAP, and RET-RGS1 were identical; GAIP differed only in Mg2+ dependence and in its slightly lower selectivity for Gα(z). RGSZ1, RET-RGS1, and GAIP thus define a subfamily of G(z) GAPs within the RGS proteins. RGSZ1 has no obvious membrane-spanning region but is tightly membrane-bound in brain. Its regulatory activity in membranes depends on stable bilayer association. When co-reconstituted into phospholipid vesicles with G(z) and m2 muscarinic receptors, RGSZ1 increased agonist- stimulated GTPase >15-fold with EC50",
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