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鉴定土壤线虫秀丽隐杆线虫内源性肽的方法。

Approaches to identify endogenous peptides in the soil nematode Caenorhabditis elegans.

作者信息

Husson Steven J, Clynen Elke, Boonen Kurt, Janssen Tom, Lindemans Marleen, Baggerman Geert, Schoofs Liliane

机构信息

Functional Genomics and Proteomics, Department of Biology, K.U. Leuven, Leuven, Belgium.

出版信息

Methods Mol Biol. 2010;615:29-47. doi: 10.1007/978-1-60761-535-4_3.

Abstract

The transparent soil nematode Caenorhabditis elegans can be considered an important model organism due to its ease of cultivation, suitability for high-throughput genetic screens, and extremely well-defined anatomy. C. elegans contains exactly 959 cells that are ordered in defined differentiated tissues. Although C. elegans only possesses 302 neurons, a large number of similarities among the neuropeptidergic signaling pathways can be observed with other metazoans. Neuropeptides are important messenger molecules that regulate a wide variety of physiological processes. These peptidergic signaling molecules can therefore be considered important drug targets or biomarkers. Neuropeptide signaling is in the nanomolar range, and biochemical elucidation of individual peptide sequences in the past without the genomic information was challenging. Since the rise of many genome-sequencing projects and the significant boost of mass spectrometry instrumentation, many hyphenated techniques can be used to explore the "peptidome" of individual species, organs, or even cell cultures. The peptidomic approach aims to identify endogenously present (neuro)peptides by using liquid chromatography and mass spectrometry in a high-throughput way. Here we outline the basic procedures for the maintenance of C. elegans nematodes and describe in detail the peptide extraction procedures. Two peptidomics strategies (off-line HPLC-MALDI-TOF MS and on-line 2D-nanoLC-Q-TOF MS/MS) and the necessary instrumentation are described.

摘要

透明土壤线虫秀丽隐杆线虫因其易于培养、适合高通量基因筛选以及解剖结构极其明确,可被视为一种重要的模式生物。秀丽隐杆线虫恰好包含959个细胞,这些细胞按特定分化组织有序排列。尽管秀丽隐杆线虫仅拥有302个神经元,但在神经肽能信号通路方面可观察到与其他后生动物存在大量相似之处。神经肽是调节多种生理过程的重要信使分子。因此,这些肽能信号分子可被视为重要的药物靶点或生物标志物。神经肽信号处于纳摩尔范围内,过去在没有基因组信息的情况下对单个肽序列进行生化解析具有挑战性。自从许多基因组测序项目兴起以及质谱仪器有了显著改进以来,许多联用技术可用于探索单个物种、器官甚至细胞培养物的“肽组”。肽组学方法旨在通过液相色谱和质谱以高通量方式鉴定内源性存在的(神经)肽。在此,我们概述了秀丽隐杆线虫的饲养基本程序,并详细描述了肽提取程序。描述了两种肽组学策略(离线HPLC-MALDI-TOF MS和在线二维纳升液相色谱-Q-TOF MS/MS)以及所需的仪器设备。

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