Walker S A, Lockyer P J, Cullen P J
The Henry Wellcome Laboratories for Integrated Cell Signalling, Inositide Group, Department of Biochemistry, University of Bristol, Bristol BS8 1TD, UK.
Biochem Soc Trans. 2003 Oct;31(Pt 5):966-9. doi: 10.1042/bst0310966.
Activation of cell-surface receptors often leads to changes in intracellular calcium concentration (Ca(2+)). Receptor-generated calcium transients are often seen as repetitive spikes of elevated intracellular calcium concentration (Ca(2+)), whose frequency varies according to the amplitude of the receptor stimuli. This suggests a requirement for molecular decoders, capable of interpreting such complex calcium signals into the correct physiological response. Ras proteins are binary molecular switches controlling a plethora of cellular responses. Whether Ras is in its active GTP-bound, or inactive GDP-bound, form is determined by the activity of guanine nucleotide exchange factors (GEFs) and GTPase-activating protein (GAPs). Calcium-regulated GEFs and GAPs have been identified, some with an exquisite sensitivity to Ca(2+), implicating a potential role of complex calcium signals in regulating Ras.
