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  • A calcium-dependent interaction between calmodulin and the calponin homology domain of human IQGAP1.

A calcium-dependent interaction between calmodulin and the calponin homology domain of human IQGAP1.

Molecular and cellular biochemistry (2012-09-05)
William J Andrews, Conor A Bradley, Elaine Hamilton, Clare Daly, Thérèse Mallon, David J Timson
ABSTRACT

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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
8-Anilino-1-naphthalenesulfonic acid ammonium salt, suitable for fluorescence, ≥97.0% (HPLC)
Sigma-Aldrich
8-Anilino-1-naphthalenesulfonic acid ammonium salt, technical, ≥90% (NT)
Sigma-Aldrich
8-Anilino-1-naphthalenesulfonic acid
Sigma-Aldrich
8-Anilino-1-naphthalenesulfonic acid hemimagnesium salt hydrate, suitable for fluorescence, ≥95.0% (T)
Sigma-Aldrich
8-Anilino-1-naphthalenesulfonic acid hemimagnesium salt hydrate, suitable for fluorescence, ≥95% (TLC)