On the Structural Biochemical Mechanism of Synaptic Neurotransmission in the Brain
Duration: 1 hour 40 mins
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Description: |
Rothman, J (Yale University)
Wednesday 13th April 2016 - 15:00 to 16:00 |
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Created: | 2016-04-15 10:19 |
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Collection: | Stochastic Dynamical Systems in Biology: Numerical Methods and Applications |
Publisher: | Isaac Newton Institute |
Copyright: | Rothman, J |
Language: | eng (English) |
Distribution: | World (downloadable) |
Explicit content: | No |
Aspect Ratio: | 16:9 |
Screencast: | No |
Bumper: | UCS Default |
Trailer: | UCS Default |
Abstract: | Neurotransmitters stored in synaptic vesicles at nerve endings are synchronously released in less than one millisecond after the action potential arrives and calcium ions secondarily enter the pre-synaptic cytoplasm. This is by far the fastest membrane fusion mechanism in nature, as is required for all thought and action. Yet, neurotransmission relies on the same SNAREpin zippering mechanism that powers more leisurely and less coherent hormone release and vesicle trafficking within the cell. How can the same molecular machine provide for such action on time scales differing by up to a factor of 10,000? Answers are emerging from mechanistic studies of the two key elements of synaptic regulatory machinery that together allow many SNAREpins to synchronize spatially and temporally. The calcium sensor, Synaptotagmin, assembles into rings that can impede fusion until they disassemble upon binding calcium ions. The rod-like Complexin molecule can organize two layers of SNAREpins into zig-zag arrays while at the same time impeding completion of zippering. |
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