Structural Insights into L-Type Voltage-Gated Ca 2+ Channel (Ca V 1.2) Activation by CaBP1

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Abstract
The L-type voltage-gated Ca2+ channel (CaV1.2) controls gene expression, cardiac function, and neuronal excitability. Mutations in CaV1.2 that disrupt channel function are implicated in cardiac arrhythmias, vascular dysfunction, Timothy Syndrome, and epilepsy. Calcium-binding protein 1 (CaBP1) binds to the IQ-motif in CaV1.2 (residues 1640-1665), blocks Ca2+-dependent inactivation (CDI), and promotes Ca2+-dependent facilitation (CDF). CaBP1 is 56% identical in sequence to calmodulin (CaM), and both proteins bind competitively to the IQ-motif. Our binding studies reveal that Ca2+ binding to CaBP1 is enhanced more than 40-fold when CaBP1 is bound to the IQ peptide. Also, the IQ peptide binds to Ca2+-bound CaBP1 (dissociation constant of 45 ± 10 nM) with 100-fold higher affinity than IQ binding to Ca2+-free CaBP1. We present NMR structures of Ca2+-CaBP1 bound to the IQ peptide, which reveal CaBP1 residues (A107, F111, M128, L131, I144, and M165) that contact IQ residues (I1654, Y1657, and F1658). Also, IQ residue K1662 forms a salt bridge with CaBP1 residue D140, which may explain why a K1662 charge reversal mutation causes 4-fold weaker IQ binding to CaBP1. Electrophysiology studies suggest that CaBP1 acts to increase the CaV1.2 channel open probability (Po). We propose that Ca2+ binding to the third and fourth EF-hands of CaBP1 and the binding of Ca2+-bound CaBP1 to the IQ-motif are important for CaV1.2 channel activation.
Funding Information
  • National Eye Institute (R01EY012347)
  • National Heart, Lung, and Blood Institute (R01 HL180444)
  • National Institute on Aging (R01AG055357)

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