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生物纳米工厂针对并激活上皮细胞表面,以调节细菌群体感应和种间信号传递。

Biological nanofactories target and activate epithelial cell surfaces for modulating bacterial quorum sensing and interspecies signaling.

机构信息

Center for Biosystems Research, University of Maryland Biotechnology Institute, 5115 Plant Science Building, College Park, Maryland 20742, United States.

出版信息

ACS Nano. 2010 Nov 23;4(11):6923-31. doi: 10.1021/nn1013066. Epub 2010 Oct 28.

Abstract

In order to control the behavior of bacteria present at the surface of human epithelial cells, we have created a biological "nanofactory" construct that "coats" the epithelial cells and "activates" the surface to produce the bacterial quorum sensing signaling molecule, autoinducer-2 (AI-2). Specifically, we demonstrate directed modulation of signaling among Escherichia coli cells grown over the surface of human epithelial (Caco-2) cells through site-directed attachment of biological nanofactories. These "factories" comprise a fusion protein expressed and purified from E. coli containing two AI-2 bacterial synthases (Pfs and LuxS), a protein G IgG binding domain, and affinity ligands for purification. The final factory is fabricated ex vivo by incubating with an anti-CD26 antibody that binds the fusion protein and specifically targets the CD26 dipeptidyl peptidase found on the outer surface of Caco-2 cells. This is the first report of the intentional "in vitro" synthesis of bacterial autoinducers at the surface of epithelial cells for the redirection of quorum sensing behaviors of bacteria. We envision tools such as this will be useful for interrogating, interpreting, and disrupting signaling events associated with the microbiome localized in human intestine and other environments.

摘要

为了控制存在于人类上皮细胞表面的细菌的行为,我们创建了一种生物“纳米工厂”构建体,它“覆盖”上皮细胞并“激活”表面以产生细菌群体感应信号分子,自诱导物-2(AI-2)。具体来说,我们通过在人类上皮(Caco-2)细胞表面生长的大肠杆菌细胞的定点附着来证明对信号的定向调制。这些“工厂”由从大肠杆菌中表达和纯化的融合蛋白组成,该融合蛋白包含两个 AI-2 细菌合酶(Pfs 和 LuxS)、一个蛋白 G IgG 结合结构域和用于纯化的亲和配体。最终的工厂是通过与抗 CD26 抗体孵育而在体外制造的,该抗体结合融合蛋白并特异性靶向 Caco-2 细胞外表面上的 CD26 二肽基肽酶。这是首次报道在体外上皮细胞表面有意合成细菌自诱导物以重新引导细菌群体感应行为。我们设想,此类工具将有助于研究、解释和破坏与人类肠道和其他环境中定殖的微生物组相关的信号事件。

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