Division of Biology and Biological Engineering , California Institute of Technology , 1200 East California Boulevard , Pasadena , California 91125-2900 , United States.
Department of Molecular Pharmacology, Physiology and Biotechnology , Brown University , Providence , Rhode Island 02912 , United States.
J Proteome Res. 2018 Nov 2;17(11):3959-3975. doi: 10.1021/acs.jproteome.8b00618. Epub 2018 Oct 4.
The α7-nicotinic acetylcholine receptor (α7-nAChR) is a ligand-gated ion channel that is expressed widely in vertebrates and is the principal high-affinity α-bungarotoxin (α-bgtx) binding protein in the mammalian CNS. α7-nAChRs associate with proteins that can modulate its properties. The α7-nAChR interactome is the summation of proteins interacting or associating with α7-nAChRs in a protein complex. To identify an α7-nAChR interactome in neural tissue, we isolated α-bgtx-affinity protein complexes from wild-type and α7-nAChR knockout (α7 KO) mouse whole brain tissue homogenates using α-bgtx-affinity beads. Affinity precipitated proteins were trypsinized and analyzed with an Orbitrap Fusion mass spectrometer. Proteins isolated with the α7-nAChR specific ligand, α-bgtx, were determined to be α7-nAChR associated proteins. The α7-nAChR subunit and 120 additional proteins were identified. Additionally, 369 proteins were identified as binding to α-bgtx in the absence of α7-nAChR expression, thereby identifying nonspecific proteins for α7-nAChR investigations using α-bgtx enrichment. These results expand on our previous investigations of α7-nAChR interacting proteins using α-bgtx-affinity bead isolation by controlling for differences between α7-nAChR and α-bgtx-specific proteins, developing an improved protein isolation methodology, and incorporating the latest technology in mass spectrometry. The α7-nAChR interactome identified in this study includes proteins associated with the expression, localization, function, or modulation of α7-nAChRs, and it provides a foundation for future studies to elucidate how these interactions contribute to human disease.
α7-烟碱型乙酰胆碱受体 (α7-nAChR) 是一种配体门控离子通道,广泛表达于脊椎动物中,是哺乳动物中枢神经系统中主要的高亲和力α-银环蛇毒素(α-bgtx)结合蛋白。α7-nAChR 与可以调节其性质的蛋白质结合。α7-nAChR 相互作用组是指在蛋白质复合物中与 α7-nAChR 相互作用或结合的蛋白质的总和。为了鉴定神经组织中的 α7-nAChR 相互作用组,我们使用 α-bgtx 亲和珠从野生型和 α7-nAChR 敲除(α7 KO)小鼠全脑组织匀浆中分离 α-bgtx 亲和蛋白复合物。用 α-bgtx 亲和珠分离的蛋白用胰蛋白酶消化,并用 Orbitrap Fusion 质谱仪进行分析。用 α7-nAChR 特异性配体 α-bgtx 分离的蛋白被鉴定为与 α7-nAChR 相关的蛋白。鉴定出了 α7-nAChR 亚基和 120 种额外的蛋白。此外,在没有 α7-nAChR 表达的情况下,还鉴定出 369 种与 α-bgtx 结合的蛋白,从而确定了使用 α-bgtx 富集进行 α7-nAChR 研究的非特异性蛋白。这些结果扩展了我们之前使用 α-bgtx 亲和珠分离鉴定 α7-nAChR 相互作用蛋白的研究,通过控制 α7-nAChR 和 α-bgtx 特异性蛋白之间的差异,开发了一种改进的蛋白质分离方法,并结合了质谱技术的最新进展。本研究鉴定的 α7-nAChR 相互作用组包括与 α7-nAChR 的表达、定位、功能或调节相关的蛋白,为进一步阐明这些相互作用如何导致人类疾病提供了基础。