Proteomic Studies of a Single CNS Synapse Type: The Parallel Fiber/Purkinje Cell Synapse

被引:47
|
作者
Selimi, Fekrije [1 ,2 ,3 ]
Cristea, Ileana M. [4 ,5 ]
Heller, Elizabeth [1 ]
Chait, Brian T. [4 ]
Heintz, Nathaniel [1 ]
机构
[1] Rockefeller Univ, Howard Hughes Med Inst, Mol Biol Lab, New York, NY 10021 USA
[2] CNRS, UMR7102, Paris, France
[3] UPMC, UMR7102, Paris, France
[4] Rockefeller Univ, Lab Mass Spectrometry & Gaseous Ion Chem, New York, NY 10021 USA
[5] Princeton Univ, Dept Mol Biol, Princeton, NJ USA
基金
美国国家卫生研究院;
关键词
POSTSYNAPTIC DENSITY FRACTION; PROTEIN-TYROSINE PHOSPHATASES; GLUTAMATE-RECEPTOR; RAT FOREBRAIN; PHOSPHOINOSITIDES; IDENTIFICATION; SUPERFAMILY; MORPHOLOGY; EXPRESSION; GRADIENT;
D O I
10.1371/journal.pbio.1000083
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Precise neuronal networks underlie normal brain function and require distinct classes of synaptic connections. Although it has been shown that certain individual proteins can localize to different classes of synapses, the biochemical composition of specific synapse types is not known. Here, we have used a combination of genetically engineered mice, affinity purification, and mass spectrometry to profile proteins at parallel fiber/Purkinje cell synapses. We identify approximately 60 candidate postsynaptic proteins that can be classified into 11 functional categories. Proteins involved in phospholipid metabolism and signaling, such as the protein kinase MRCK gamma, are major unrecognized components of this synapse type. We demonstrate that MRCK gamma can modulate maturation of dendritic spines in cultured cortical neurons, and that it is localized specifically to parallel fiber/Purkinje cell synapses in vivo. Our data identify a novel synapse-specific signaling pathway, and provide an approach for detailed investigations of the biochemical complexity of central nervous system synapse types.
引用
收藏
页码:948 / 957
页数:10
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