Proteomic Analysis of Unbounded Cellular Compartments: Synaptic Clefts.

Proteomic Analysis of Unbounded Cellular Compartments: Synaptic Clefts.
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DOI:
10.1016/j.cell.2016.07.041
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发表时间:
2016-08-25
期刊:
影响因子:
64.5
通讯作者:
Ting, Alice Y.
Ting, Alice Y.
中科院分区:
生物学1区
文献类型:
--
作者:
Loh, Ken H.;Stawski, Philipp S.;Draycott, Austin S.;Udeshi, Namrata D.;Lehrman, Emily K.;Wilton, Daniel K.;Svinkina, Tanya;Deerinck, Thomas J.;Ellisman, Mark H.;Stevens, Beth;Carr, Steven A.;Ting, Alice Y.

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Cellular compartments that cannot be biochemically isolated are challenging to characterize. Here we demonstrate the proteomic characterization of the synaptic clefts that exist at both excitatory and inhibitory synapses. Normal brain function relies on the careful balance of these opposing neural connections, and understanding how this balance is achieved relies on knowledge of their protein compositions. Using a spatially restricted enzymatic tagging strategy, we mapped the proteomes of two of the most common excitatory and inhibitory synaptic clefts in living neurons. These proteomes reveal dozens of synaptic candidates, and assign numerous known synaptic proteins to a specific cleft type. The molecular differentiation of each cleft allowed us to identify Mdga2 as a potential specificity factor influencing Neuroligin-2's recruitment of presynaptic neurotransmitters at inhibitory synapses.
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