TY - JOUR
T1 - Doc2b is a high-affinity Ca2+sensor for spontaneous neurotransmitter release
AU - Groffen, Alexander J.
AU - Martens, Sascha
AU - Arazola, Rocío Diez
AU - Cornelisse, L. Niels
AU - Lozovaya, Natalia
AU - De Jong, Arthur P.H.
AU - Goriounova, Natalia A.
AU - Habets, Ron L.P.
AU - Takai, Yoshimi
AU - Borst, J. Gerard
AU - Brose, Nils
AU - McMahon, Harvey T.
AU - Verhage, Matthijs
PY - 2010/3/26
Y1 - 2010/3/26
N2 - Synaptic vesicle fusion in brain synapses occurs in phases that are either tightly coupled to action potentials (synchronous), immediately following action potentials (asynchronous), or as stochastic events in the absence of action potentials (spontaneous). Synaptotagmin-1, -2, and -9 are vesicleassociated Ca2+ sensors for synchronous release. Here we found that double C2 domain (Doc2) proteins act as Ca2+ sensors to trigger spontaneous release. Although Doc2 proteins are cytosolic, they function analogously to synaptotagmin-1 but with a higher Ca2+ sensitivity. Doc2 proteins bound to N-ethylmaleimidesensitive factor attachment receptor (SNARE) complexes in competition with synaptotagmin-1. Thus, different classes of multiple C2 domain-containing molecules trigger synchronous versus spontaneous fusion, which suggests a general mechanism for synaptic vesicle fusion triggered by the combined actions of SNAREs and multiple C2 domain-containing proteins.
AB - Synaptic vesicle fusion in brain synapses occurs in phases that are either tightly coupled to action potentials (synchronous), immediately following action potentials (asynchronous), or as stochastic events in the absence of action potentials (spontaneous). Synaptotagmin-1, -2, and -9 are vesicleassociated Ca2+ sensors for synchronous release. Here we found that double C2 domain (Doc2) proteins act as Ca2+ sensors to trigger spontaneous release. Although Doc2 proteins are cytosolic, they function analogously to synaptotagmin-1 but with a higher Ca2+ sensitivity. Doc2 proteins bound to N-ethylmaleimidesensitive factor attachment receptor (SNARE) complexes in competition with synaptotagmin-1. Thus, different classes of multiple C2 domain-containing molecules trigger synchronous versus spontaneous fusion, which suggests a general mechanism for synaptic vesicle fusion triggered by the combined actions of SNAREs and multiple C2 domain-containing proteins.
UR - http://www.scopus.com/inward/record.url?scp=77950286800&partnerID=8YFLogxK
U2 - https://doi.org/10.1126/science.1183765
DO - https://doi.org/10.1126/science.1183765
M3 - Article
C2 - 20150444
SN - 0036-8075
VL - 327
SP - 1614
EP - 1618
JO - Science
JF - Science
IS - 5973
ER -