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通过用胞内抗体阻断受体细胞内的松弛酶活性,可以抑制接合转移。

Conjugative transfer can be inhibited by blocking relaxase activity within recipient cells with intrabodies.

作者信息

Garcillán-Barcia M Pilar, Jurado Paola, González-Pérez Blanca, Moncalián Gabriel, Fernández Luis A, de la Cruz Fernando

机构信息

Departamento de Biología Molecular (Laboratorio asociado al Centro de Investigaciones Biológicas, C.S.I.C.), Universidad de Cantabria, C/Cardenal Herrera Oria s/n, 39011 Santander, Spain.

出版信息

Mol Microbiol. 2007 Jan;63(2):404-16. doi: 10.1111/j.1365-2958.2006.05523.x. Epub 2006 Dec 5.

Abstract

Horizontal transfer of antibiotic resistance genes carried by conjugative plasmids poses a serious health problem. As conjugative relaxases are transported to recipient cells during bacterial conjugation, we investigated whether blocking relaxase activity in the recipient cell might inhibit conjugation. For that purpose, we used an intrabody approach generating a single-chain Fv antibody library against the relaxase TrwC of conjugative plasmid R388. Recombinant single-chain Fv antibodies were engineered for cytoplasmic expression in Escherichia coli cells and either selected in vitro for their specific binding to TrwC, or in vivo by their ability to interfere with conjugation using a high-throughput mating assay. Several intrabody clones were identified showing specific inhibition against R388 conjugation upon cytoplasmic expression in the recipient cell. The epitope recognized by one of these intrabodies was mapped to a region of TrwC containing Tyr-26 and involved in the conjugative DNA-processing termination reaction. These findings demonstrate that the transferred relaxase plays an important role in the recipient cell and open a new approach to identify specific inhibitors of bacterial conjugation.

摘要

接合质粒携带的抗生素抗性基因的水平转移构成了一个严重的健康问题。由于在细菌接合过程中接合松弛酶会被转运到受体细胞中,我们研究了在受体细胞中阻断松弛酶活性是否可能抑制接合。为此,我们采用了一种胞内抗体方法,构建了一个针对接合质粒R388的松弛酶TrwC的单链Fv抗体文库。重组单链Fv抗体经工程改造后可在大肠杆菌细胞中进行胞质表达,要么在体外根据其与TrwC的特异性结合进行筛选,要么在体内通过使用高通量交配试验干扰接合的能力进行筛选。鉴定出了几个胞内抗体克隆,它们在受体细胞中进行胞质表达时对接合质粒R388的接合表现出特异性抑制作用。其中一种胞内抗体识别的表位被定位到TrwC的一个包含酪氨酸-26且参与接合性DNA加工终止反应的区域。这些发现表明,转移的松弛酶在受体细胞中起着重要作用,并为鉴定细菌接合的特异性抑制剂开辟了一条新途径。

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