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{"title":"Quantitative Proteomic Profiling of Cryptococcus neoformans","authors":"Brianna Ball, Jennifer Geddes-McAlister","doi":"10.1002/cpmc.94","DOIUrl":null,"url":null,"abstract":"Cryptococcus neoformans is an opportunistic human fungal pathogen commonly associated with infection in immunocompromised individuals (e.g., patients with HIV/AIDS). Important virulence determinants include the production of a polysaccharide capsule, melanin, and extracellular enzymes, as well as the ability to grow at 37°C. C. neoformans controls a plethora of host defense and evasion mechanisms to survive during infection and to proliferate within the host, causing meningoencephalitis and death. Traditionally, characterization of C. neoformans under different environmental conditions and stresses has relied on genetic and phenotypic analyses, as well as biochemical assays. However, advances in mass spectrometry instrumentation, sample preparation protocols, and bioinformatic tools and databases promote comprehensive profiling of fungal cellular processes, secretion or protein release into the extracellular environment, and vesicle contents. Moreover, proteomics provides insight into regulatory mechanisms influencing signal transduction cascades and protein complexes or networks through profiling of post‐translational modifications and protein–protein interactions. Given the medical impact of C. neoformans infections and the recent emergence of antifungal‐resistant strains, defining proteins produced in response to unique environments provides an opportunity to uncover antivirulence strategies and alternative therapeutic options to combat infection. Here, we describe culturing and sample preparation of C. neoformans and outline protocols for comprehensively profiling changes in protein abundance within the cellular proteome and secretome. © 2019 by John Wiley & Sons, Inc.","PeriodicalId":39967,"journal":{"name":"Current Protocols in Microbiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2019-12-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/cpmc.94","citationCount":"12","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Protocols in Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/cpmc.94","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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新生隐球菌的定量蛋白质组学分析
新型隐球菌是一种机会性人类真菌病原体,通常与免疫功能低下个体(例如艾滋病毒/艾滋病患者)的感染有关。重要的毒力决定因素包括多糖胶囊、黑色素和细胞外酶的产生,以及在37℃下生长的能力。新生隐球菌控制了大量的宿主防御和逃避机制,以便在感染期间存活并在宿主内增殖,导致脑膜脑炎和死亡。传统上,在不同的环境条件和胁迫下,新形态C.的表征依赖于遗传和表型分析,以及生化分析。然而,质谱仪器、样品制备方案、生物信息学工具和数据库的进步促进了真菌细胞过程、分泌或蛋白质释放到细胞外环境以及囊泡内容物的全面分析。此外,蛋白质组学通过分析翻译后修饰和蛋白质相互作用,提供了影响信号转导级联和蛋白质复合物或网络的调控机制。鉴于新生梭状菌感染的医学影响和最近出现的抗真菌耐药菌株,定义响应独特环境产生的蛋白质提供了揭示抗毒策略和对抗感染的替代治疗方案的机会。在这里,我们描述了C. neoformans的培养和样品制备,并概述了在细胞蛋白质组和分泌组中全面分析蛋白质丰度变化的方案。©2019 by John Wiley &基本方案1:新隐球菌的生长和样品制备基本方案2:从上清中提取蛋白质基本方案3:从细胞颗粒中提取蛋白质基本方案4:蛋白质组学分析和生物信息学
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