Structures of CaV2 Ca2+/CaM-IQ domain complexes reveal binding modes that underlie calcium-dependent inactivation and facilitation.
Structures of CaV2 Ca2+/CaM-IQ domain complexes reveal binding modes that underlie calcium-dependent inactivation and facilitation.
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DOI:
10.1016/j.str.2008.07.010
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发表时间:
2008-10-08
期刊:
影响因子:
--
通讯作者:
Minor DL Jr
中科院分区:
文献类型:
--
作者:
Kim EY;Rumpf CH;Fujiwara Y;Cooley ES;Van Petegem F;Minor DL Jr
Calcium influx drives two opposing voltage-activated calcium channel (CaV) self-modulatory processes: calcium-dependent inactivation (CDI) and calcium-dependent facilitation (CDF). Specific Ca2+/calmodulin (Ca2+/CaM) lobes produce CDI and CDF through interactions with the CaVα1 subunit IQ domain. Curiously, Ca2+/CaM lobe modulation polarity appears inverted between CaV1s and CaV2s. Here, we present crystal structures of CaV2.1, CaV2.2, and CaV2.3 Ca2+/CaM-IQ domain complexes. All display binding orientations opposite to CaV1.2 with a physical reversal of the CaM lobe positions relative to the IQ α-helix. Titration calorimetry reveals lobe competition for a high-affinity site common to CaV1 and CaV2 IQ domains that is occupied by the CDI lobe in the structures. Electrophysiological experiments demonstrate that the N-terminal CaV2 Ca2+/C-lobe anchors affect CDF. Together, the data unveil the remarkable structural plasticity at the heart of CaV feedback modulation and indicate that CaV1 and CaV2 IQ domains bear a dedicated CDF site that exchanges Ca2+/CaM lobe occupants.
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DOI:
10.1085/jgp.200709786
发表时间:
2007-05
期刊:
The Journal of general physiology
影响因子:
--
作者:
Dunlap K
通讯作者:
Dunlap K
影响因子:
7.8
作者:
Hudmon, A;Schulman, H;Kim, J;Maltez, JM;Tsien, RW;Pitt, GS
通讯作者:
Pitt, GS
影响因子:
5.7
作者:
Fallon, JL;Halling, DB;Quiocho, FA
通讯作者:
Quiocho, FA
影响因子:
64.8
作者:
Drum, CL;Yan, SZ;Tang, WJ
通讯作者:
Tang, WJ
DOI:
10.1073/pnas.0710213105
发表时间:
2008-01-08
影响因子:
11.1
作者:
Jiang, Xin;Lautermilch, Nathan J.;Catterall, William A.
通讯作者:
Catterall, William A.