脑脊液
蛋白质组
蛋白质组学
内生
生物标志物
疾病
糖基化
化学
计算生物学
生物标志物发现
医学
病理
生物
神经科学
生物化学
基因
作者
Danqing Wang,Zhengwei Chen,Lingjun Li
标识
DOI:10.1007/978-1-0716-3646-6_24
摘要
Human cerebrospinal fluid (CSF) is a rich source for central nervous systemNervous systems (CNS)-related disease biomarker discovery due to its direct interchange with the extracellular fluid of the CNS. Though extensive proteome-level profiling has been conducted for CSF, studies targeting at its endogenous peptidome is still limited. It is more difficult to include the post-translational modifications (PTMs) characterization of the peptidome in the mass spectrometry (MS) analysis because of their low abundance and the challenge of data interpretation. In this chapter, we present a peptidomic workflow that combines molecular weight cut-off (MWCO) separation, electron-transfer and higher-energy collision dissociation (EThcD) fragmentation, and a three-step database searching strategy for comprehensive PTMPost-translational modification (PTM) analysis of endogenous peptides including both N-glycosylation and O-glycosylation and other common peptide PTMs. The method has been successfully adopted to analyze CSF samples from healthy donors, mild cognitive impairment (MCI), and Alzheimer's disease (AD)Alzheimer's disease (AD) patients to provide a landscape of peptidome in different disease states.
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