Doc2b Is a High-Affinity Ca 2+ Sensor for Spontaneous Neurotransmitter Release

Author:

Groffen Alexander J.1,Martens Sascha2,Arazola Rocío Díez1,Cornelisse L. Niels1,Lozovaya Natalia134,de Jong Arthur P. H.1,Goriounova Natalia A.13,Habets Ron L. P.5,Takai Yoshimi5,Borst J. Gerard4,Brose Nils6,McMahon Harvey T.2,Verhage Matthijs1

Affiliation:

1. Department of Functional Genomics, CNCR, Neuroscience Campus Amsterdam, VU University and VU Medical Center, Amsterdam, 1081 HV, Netherlands.

2. Medical Research Council (MRC) Laboratory of Molecular Biology, Hills Road, Cambridge, CB2 0QH, UK.

3. Department of Integrative Neurophysiology, CNCR, VU University, Amsterdam, 1081 HV, Netherlands.

4. Bogomoletz Institute of Physiology, Kiev, 01024, Ukraine.

5. Department of Neuroscience, Erasmus MC, University Medical Center, Rotterdam, 3000 CA, Netherlands.

6. Department of Biochemistry and Molecular Biology, Kobe University Graduate School of Medicine, Kobe 650-0017, Japan.

Abstract

“Spontaneous” Release Trigger Synaptic vesicle release occurs in different phases that can be tightly coupled to action potentials (synchronous), immediately following action potentials (asynchronous), or as stochastic events not triggered by action potentials (spontaneous). The vesicle protein synaptotagmin is thought to act as the Ca 2+ sensor in the synchronous phase, but for the other two phases, Ca 2+ sensors have not been identified. Groffen et al. (p. 1614 , published online 11 February) now show that cytoplasmic proteins known as Doc2 (double C2 domain) proteins are required for spontaneous release. Doc2 proteins promote membrane fusion in response to exceptionally low increases in Ca 2+ , and are several orders of magnitude more sensitive to Ca 2+ than synaptotagmin. Doc2 and synaptotagmin compete for SNARE-complex binding during membrane fusion. A mutation that abolishes the Ca 2+ dependence of Doc2b also abolishes the Ca 2+ dependence of spontaneous release. Thus, Doc2 is a high-affinity Ca 2+ sensor for spontaneous release that competes with synaptotagmin for SNARE complex binding.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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