TY - JOUR
T1 - Arrestin is required for agonist-induced trafficking of voltage-dependent calcium channels
AU - Puckerin, Akil
AU - Liu, Lanying
AU - Permaul, Natasha
AU - Carman, Paul
AU - Lee, Jessica
AU - Diversé-Pierluissi, María A.
PY - 2006/10/13
Y1 - 2006/10/13
N2 - Many metabotropic receptors in the nervous system act through signaling pathways that result in the inhibition of voltage-dependent calcium channels. Our previous findings showed that activation of seven-transmembrane receptors results in the internalization of calcium channels. This internalization takes place within a few seconds, raising the question of whether the endocytic machinery is in close proximity to the calcium channel to cause such rapid internalization. Here we show that voltage-dependent calcium channels are pre-associated with arrestin, a protein known to play a role in receptor trafficking. Upon GABAB receptor activation, receptors are recruited to the arrestin-channel complex and internalized. β-Arrestin 1 selectively binds to the SNARE-binding region of the calcium channel. Peptides containing the arrestin-binding site of the channel disrupt agonist-induced channel internalization. Taken together these data suggest a novel neuronal role for arrestin.
AB - Many metabotropic receptors in the nervous system act through signaling pathways that result in the inhibition of voltage-dependent calcium channels. Our previous findings showed that activation of seven-transmembrane receptors results in the internalization of calcium channels. This internalization takes place within a few seconds, raising the question of whether the endocytic machinery is in close proximity to the calcium channel to cause such rapid internalization. Here we show that voltage-dependent calcium channels are pre-associated with arrestin, a protein known to play a role in receptor trafficking. Upon GABAB receptor activation, receptors are recruited to the arrestin-channel complex and internalized. β-Arrestin 1 selectively binds to the SNARE-binding region of the calcium channel. Peptides containing the arrestin-binding site of the channel disrupt agonist-induced channel internalization. Taken together these data suggest a novel neuronal role for arrestin.
UR - http://www.scopus.com/inward/record.url?scp=33750051637&partnerID=8YFLogxK
U2 - 10.1074/jbc.M605000200
DO - 10.1074/jbc.M605000200
M3 - Article
C2 - 16912040
AN - SCOPUS:33750051637
SN - 0021-9258
VL - 281
SP - 31131
EP - 31141
JO - Journal of Biological Chemistry
JF - Journal of Biological Chemistry
IS - 41
ER -