Abstract
Both the α- and βγ-subunits of heterotrimeric guanine nucleotide dependent regulatory proteins (G-proteins) couple members of the heptahelical class of cell-surface receptors to a diverse range of signal generating effectors including retinal cyclic GMP phosphodiesterase, ion channels, adenylylcyclases, phosphoinositide kinase, and members of the β-class of inositol lipid-specific phospholipases C. Although the molecular details of the G-protein-regulated phospholipase C system were elucidated comparatively recently, these enzymes have become an important model for investigations of the process of G protein effector coupling. A combination of molecular biological, biochemical, and structural studies using the phospholipase C-β enzymes has provided some important; insights into the interplay between G-proteins and their effecters and promises to reveal the mechanisms by which G protein α- and βγ-subunits selectively associate with and activate effecters.
| Original language | English |
|---|---|
| Pages (from-to) | 429-435 |
| Number of pages | 7 |
| Journal | Biochemical Pharmacology |
| Volume | 54 |
| Issue number | 4 |
| DOIs |
|
| State | Published - Aug 15 1997 |
Keywords
- G-protein
- Hormone
- Phospholipase C
- Phospholipids
- Receptor
- Signal transduction
ASJC Scopus subject areas
- Biochemistry
- Pharmacology
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