TY - JOUR
T1 - The voltage-gated calcium-channel β subunit
T2 - More than just an accessory
AU - Karunasekara, Yamuna
AU - Dulhunty, Angela F.
AU - Casarotto, Marco G.
PY - 2009/1
Y1 - 2009/1
N2 - Voltage-gated Ca2+ channels (VGCCs) are involved in a number of excitatory processes in the cell that regulate muscle contraction, neurotransmitter release, gene regulation, and neuronal migration. They consist of a central pore-forming α1 subunit together with a number of associated auxiliary subunits including a cytoplasmic β subunit. With the aid of X-ray crystallography, it has been found that the β subunits of VGCCs (β2a, β3, and β4) interact strongly with the I-II loop of the pore-forming α1 subunit. Here we discuss the potential interaction sites of β1a with its α1 subunit as well as the skeletal ryanodine receptor. We suggest that not only can β1a interact with the α1 subunit I-II loop, but more subtle interactions may be possible through the II-III loop via the β1a SH3 domain. Such findings could have important implications with respect to EC coupling.
AB - Voltage-gated Ca2+ channels (VGCCs) are involved in a number of excitatory processes in the cell that regulate muscle contraction, neurotransmitter release, gene regulation, and neuronal migration. They consist of a central pore-forming α1 subunit together with a number of associated auxiliary subunits including a cytoplasmic β subunit. With the aid of X-ray crystallography, it has been found that the β subunits of VGCCs (β2a, β3, and β4) interact strongly with the I-II loop of the pore-forming α1 subunit. Here we discuss the potential interaction sites of β1a with its α1 subunit as well as the skeletal ryanodine receptor. We suggest that not only can β1a interact with the α1 subunit I-II loop, but more subtle interactions may be possible through the II-III loop via the β1a SH3 domain. Such findings could have important implications with respect to EC coupling.
KW - Beta subunit
KW - Dihydropyridine receptor
KW - Excitation contraction (EC) coupling
KW - Voltage-gated calcium channels
UR - http://www.scopus.com/inward/record.url?scp=70450252291&partnerID=8YFLogxK
U2 - 10.1007/s00249-009-0467-4
DO - 10.1007/s00249-009-0467-4
M3 - Review article
SN - 0175-7571
VL - 39
SP - 75
EP - 81
JO - European Biophysics Journal
JF - European Biophysics Journal
IS - 1
ER -