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A complex of Protocadherin-19 and N-cadherin mediates a novel mechanism of cell adhesion.原钙黏蛋白 19 和 N 钙黏蛋白复合物介导细胞黏附的新机制。
J Cell Biol. 2011 Dec 26;195(7):1115-21. doi: 10.1083/jcb.201108115. Epub 2011 Dec 19.
2
Intrinsically disordered proteins: regulation and disease.无规则卷曲蛋白质:调控与疾病
Curr Opin Struct Biol. 2011 Jun;21(3):432-40. doi: 10.1016/j.sbi.2011.03.011. Epub 2011 Apr 20.
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Intrinsically disordered proteins from A to Z.从 A 到 Z 解析无规则卷曲蛋白质
Int J Biochem Cell Biol. 2011 Aug;43(8):1090-103. doi: 10.1016/j.biocel.2011.04.001. Epub 2011 Apr 8.
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Protocadherin-19 and N-cadherin interact to control cell movements during anterior neurulation.原钙黏蛋白 19 和 N-钙黏蛋白相互作用,控制前神经胚层细胞运动。
J Cell Biol. 2010 Nov 29;191(5):1029-41. doi: 10.1083/jcb.201007008.
5
New insights into the evolution of metazoan cadherins.后生动物钙黏蛋白进化的新见解。
Mol Biol Evol. 2011 Jan;28(1):647-57. doi: 10.1093/molbev/msq233. Epub 2010 Sep 3.
6
Combinatorial homophilic interaction between gamma-protocadherin multimers greatly expands the molecular diversity of cell adhesion.γ-原钙黏蛋白多聚体的组合同性相互作用极大地扩展了细胞黏附的分子多样性。
Proc Natl Acad Sci U S A. 2010 Aug 17;107(33):14893-8. doi: 10.1073/pnas.1004526107. Epub 2010 Aug 2.
7
Phosphorylation of protocadherin proteins by the receptor tyrosine kinase Ret.原钙黏蛋白蛋白的磷酸化作用由受体酪氨酸激酶 Ret 所介导。
Proc Natl Acad Sci U S A. 2010 Aug 3;107(31):13894-9. doi: 10.1073/pnas.1007182107. Epub 2010 Jun 25.
8
Proteomics analysis reveals overlapping functions of clustered protocadherins.蛋白质组学分析揭示了聚类原钙黏蛋白的重叠功能。
Mol Cell Proteomics. 2010 Jan;9(1):71-83. doi: 10.1074/mcp.M900343-MCP200. Epub 2009 Oct 20.
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Characterizing the initial encounter complex in cadherin adhesion.描述钙黏蛋白黏附的初始接触复合物。
Structure. 2009 Aug 12;17(8):1075-81. doi: 10.1016/j.str.2009.06.012. Epub 2009 Jul 30.
10
Protocadherin-alpha family is required for serotonergic projections to appropriately innervate target brain areas.原钙黏蛋白α家族是5-羟色胺能投射适当支配靶脑区所必需的。
J Neurosci. 2009 Jul 22;29(29):9137-47. doi: 10.1523/JNEUROSCI.5478-08.2009.

聚类原钙黏蛋白 Pcdhα 和 Pcdhγ 在斑马鱼中形成异源二聚体复合物。

The clustered protocadherins Pcdhα and Pcdhγ form a heteromeric complex in zebrafish.

机构信息

Department of Neuroscience, Ohio State University, Columbus, OH 43210, USA.

出版信息

Neuroscience. 2012 Sep 6;219:280-9. doi: 10.1016/j.neuroscience.2012.05.058. Epub 2012 Jun 1.

DOI:10.1016/j.neuroscience.2012.05.058
PMID:22659564
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3402709/
Abstract

The clustered protocadherin genes encode a diverse collection of neuronal cell surface receptors. These genes have been proposed to play roles in axon targeting, synaptic development and neuronal survival, although their specific cellular roles remain poorly defined. In zebrafish there are four clustered protocadherin genes, two pcdhα clusters and two pcdhγ clusters, that give rise to over 100 distinct proteins, each with a distinct ectodomain (EC). The zebrafish is an excellent model in which to address the function of protocadherins during neural development, as the embryos are transparent, develop rapidly, and are amenable to experimental manipulation. As a first step to investigating the clustered protocadherins during zebrafish development, we have generated antibodies against the common cytodomains of zebrafish Pcdhγ. We compare the distribution of Pcdhγ with Pcdhα and find a similar pan-neuronal pattern, with strong labeling of neurons within all major regions of the central nervous system. Pcdhα and Pcdhγ are particularly enriched in the developing visual system, with strong labeling found in the synaptic layers of the retina, as well as the optic tectum. Consistent with studies in mouse, we find that Pcdhα and Pcdhγ are present in a complex, as they can be co-immunoprecipitated from zebrafish larval extracts. This interaction is direct and occurs through the ECs of these proteins. Using standard bead aggregation assays, we find no evidence for intrinsic adhesive ability by either Pcdhγ or Pcdhα, suggesting that they do not function as cell adhesion molecules.

摘要

聚类原钙黏蛋白基因编码了多种神经元细胞表面受体。这些基因被认为在轴突靶向、突触发育和神经元存活中发挥作用,尽管它们的具体细胞功能仍未得到明确界定。在斑马鱼中,有四个聚类原钙黏蛋白基因,两个 pcdhα 聚类和两个 pcdhγ 聚类,它们产生了 100 多种不同的蛋白质,每种蛋白质都有独特的细胞外结构域 (EC)。斑马鱼是研究原钙黏蛋白在神经发育过程中功能的理想模型,因为胚胎透明、发育迅速,且易于进行实验操作。作为研究斑马鱼发育过程中聚类原钙黏蛋白的第一步,我们生成了针对斑马鱼 Pcdhγ 共同细胞结构域的抗体。我们比较了 Pcdhγ 的分布与 Pcdhα 的分布,发现它们具有相似的全神经元模式,在中枢神经系统的所有主要区域内,神经元都有强烈的标记。Pcdhα 和 Pcdhγ 在发育中的视觉系统中特别丰富,在视网膜的突触层以及视顶盖中都有强烈的标记。与在小鼠中的研究一致,我们发现 Pcdhα 和 Pcdhγ 存在于复合物中,因为它们可以从斑马鱼幼虫提取物中共同免疫沉淀。这种相互作用是直接的,发生在这些蛋白质的 EC 之间。使用标准的珠子聚集测定法,我们没有发现 Pcdhγ 或 Pcdhα 具有内在粘附能力的证据,这表明它们不作为细胞粘附分子发挥作用。