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对单核细胞感染柯克斯体反应的蛋白质组学和系统生物学分析。

Proteomic and systems biology analysis of the monocyte response to Coxiella burnetii infection.

机构信息

Department of Chemistry and Biochemistry, Montana State University, Bozeman, Montana, United States of America.

出版信息

PLoS One. 2013 Aug 21;8(8):e69558. doi: 10.1371/journal.pone.0069558. eCollection 2013.

Abstract

Coxiella burnetii is an obligate intracellular bacterial pathogen and the causative agent of Q fever. Chronic Q fever can produce debilitating fatigue and C. burnetii is considered a significant bioterror threat. C. burnetii occupies the monocyte phagolysosome and although prior work has explained features of the host-pathogen interaction, many aspects are still poorly understood. We have conducted a proteomic investigation of human Monomac I cells infected with the Nine Mile Phase II strain of C. burnetii and used the results as a framework for a systems biology model of the host response. Our principal methodology was multiplex differential 2D gel electrophoresis using ZDyes, a new generation of covalently linked fluorescent protein detection dyes under development at Montana State University. The 2D gel analysis facilitated the detection of changes in posttranslational modifications on intact proteins in response to infection. The systems model created from our data a framework for the design of experiments to seek a deeper understanding of the host-pathogen interactions.

摘要

贝氏考克斯体是一种专性细胞内细菌病原体,也是 Q 热的病原体。慢性 Q 热可导致使人虚弱的疲劳,而贝氏考克斯体被认为是一种重大的生物恐怖威胁。贝氏考克斯体占据着单核细胞吞噬溶酶体,尽管先前的工作已经解释了宿主-病原体相互作用的特征,但仍有许多方面尚未得到很好的理解。我们对感染九英里 II 期菌株的单核细胞株 I 细胞进行了蛋白质组学研究,并将结果作为宿主反应系统生物学模型的框架。我们的主要方法是使用 ZDyes 进行多重差异 2D 凝胶电泳,ZDyes 是蒙大拿州立大学正在开发的新一代共价连接荧光蛋白检测染料。2D 凝胶分析有助于检测感染后完整蛋白质上翻译后修饰的变化。我们从数据中创建的系统模型为设计实验提供了一个框架,以寻求更深入地了解宿主-病原体相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2380/3749201/4bb4e316b054/pone.0069558.g001.jpg

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