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A calcium-dependent interaction between calmodulin and the calponin homology domain of human IQGAP1
被引:0
|作者:
William J. Andrews
Conor A. Bradley
Elaine Hamilton
Clare Daly
Thérèse Mallon
David J. Timson
机构:
[1] Queen’s University Belfast,School of Biological Sciences
[2] Medical Biology Centre,Belfast Metropolitan College
[3] Castlereagh Campus,undefined
来源:
关键词:
CHD;
Cytoskeletal scaffolding protein;
Calcium-dependent interaction;
Protein–protein crosslinking;
ANS displacement assay;
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摘要:
IQGAPs are cytoskeletal scaffolding proteins which collect information from a variety of signalling pathways and pass it on to the microfilaments and microtubules. There is a well-characterised interaction between IQGAP and calmodulin through a series of IQ-motifs towards the middle of the primary sequence. However, it has been shown previously that the calponin homology domain (CHD), located at the N-terminus of the protein, can also interact weakly with calmodulin. Using a recombinant fragment of human IQGAP1 which encompasses the CHD, we have demonstrated that the CHD undergoes a calcium ion-dependent interaction with calmodulin. The CHD can also displace the hydrophobic fluorescent probe 1-anilinonaphthalene-8-sulphonate from calcium–calmodulin, suggesting that the interaction involves non-polar residues on the surface of calmodulin. Molecular modelling identified a possible site on the CHD for calmodulin interaction. The physiological significance of this interaction remains to be discovered.
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页码:217 / 223
页数:6
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