Guanine nucleotide dependent and independent reconstitution of G‐proteins with adenylate cyclase: stimulation or attenuation of the enzyme by Gi α subunits

FEBS Letters

Klee, Werner A.¹  Newton, Dianne L.¹ 

[1] Laboratory of Molecular Biology, National Institute of Mental Health, Bethesda, MD 20892, USA

关键词: Adenylate cyclase;    G protein;    Reconstitution;    G-protein;    guanine nucleotide-binding protein;    CHAPS;    (3-[(3-cholamidopropyl)dimethylammonio]-1-propane sulfonate);    CHAPSO;    3-(3-cholamidopropyldimethylammonio)-1-(2-hydroxy-1-propanesulfonate);    EDTA;    ethylenediaminetetraacetic acid;    EGTA;    ethylene glycol bis(β-aminoethyl ether)-N;    N;    N';    N'-tetraacetic acid;    SDS;    sodium dodecyl sulfate;    DTT;    dithiothreitol;    GTPγS;    guanosine 5'-O-(3-thiotriphosphate);    GppNHp;    guanosine 5'-(β;    γ-imido)triphosphate;   

DOI  :  10.1016/0014-5793(90)80407-A

学科分类：生物化学/生物物理

来源: John Wiley & Sons Ltd.

【 摘 要 】

The α subunits of five members of the Gi family of bovine brain proteins were reconstituted with adenylate cyclase in phospholipid vesicles. Our results support both the views that much of the inhibition of the enzyme by Gi is due to the action of its liberated βγ subunits, and that the α subunits themselves interact with the enzyme. Inhibition of basal or Gs-stimulated adenylate cyclase activity is small or undetectable by a subunits of Go, Go^∗ and Gi-2B. On the other hand, adenylate cyclase activity is stimulated by the α subunits of Gi-1 and Gi-2A. The G proteins act in the absence of added GTP when reconstituted with phospholipids of low but not high fluidity.

【 授权许可】

Unknown