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鼠脑基因定义细胞类型的神经肽组学。

Neuropeptidomics of Genetically Defined Cell Types in Mouse Brain.

机构信息

Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY, USA.

出版信息

Methods Mol Biol. 2024;2758:213-225. doi: 10.1007/978-1-0716-3646-6_11.

Abstract

Peptidomic techniques are powerful tools to identify peptides in a biological sample. In the case of brain, which contains a complex mixture of cell types, standard peptidomics procedures reveal the major peptides in a dissected brain region. It is difficult to obtain information on peptides within a specific cell type using standard approaches, unless that cell type can be isolated. This protocol describes a targeted peptidomic approach that uses affinity chromatography to purify peptides that are substrates of carboxypeptidase E (CPE), an enzyme present in the secretory pathway of neuroendocrine cells. Many CPE products function as neuropeptides and/or peptide hormones, and therefore represent an important subset of the peptidome. Because CPE removes C-terminal Lys and Arg residues from peptide processing intermediates, organisms lacking CPE show a large decrease in the levels of the mature forms of most neuropeptides and peptide hormones, and a very large increase in the levels of the processing intermediates that contain C-terminal Lys and/or Arg (i.e., the CPE substrates). These CPE substrates can be purified on an anhydrotrypsin-agarose affinity resin, which specifically binds peptides with C-terminal basic residues. When this method is used with mice lacking CPE activity in genetically defined cell types, it allows the detection of peptides specifically produced in that cell type.

摘要

肽组学技术是鉴定生物样本中肽的有力工具。在大脑中,含有复杂的细胞类型混合物,标准的肽组学程序可以揭示脑区中主要的肽。使用标准方法很难获得特定细胞类型内的肽信息,除非可以分离该细胞类型。本方案描述了一种靶向肽组学方法,该方法使用亲和层析来纯化羧肽酶 E(CPE)的底物肽,CPE 是神经内分泌细胞分泌途径中的一种酶。许多 CPE 产物作为神经肽和/或肽激素发挥作用,因此代表了肽组的一个重要子集。由于 CPE 从肽加工中间产物中去除 C 末端赖氨酸和精氨酸残基,缺乏 CPE 的生物体中大多数神经肽和肽激素的成熟形式的水平会大幅下降,而含有 C 末端赖氨酸和/或精氨酸的加工中间产物的水平会大幅增加(即 CPE 底物)。这些 CPE 底物可以在无水胰蛋白酶-琼脂糖亲和树脂上进行纯化,该树脂特异性结合具有 C 末端碱性残基的肽。当将该方法用于在遗传定义的细胞类型中缺乏 CPE 活性的小鼠时,它可以检测到特定于该细胞类型产生的肽。

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