Biological nanofactories facilitate spatially selective capture and manipulation of quorum sensing bacteria in a bioMEMS device

被引:34
作者
Fernandes, Rohan [1 ,2 ]
Luo, Xiaolong [1 ,2 ]
Tsao, Chen-Yu [1 ,2 ]
Payne, Gregory F. [2 ]
Ghodssi, Reza [3 ,4 ]
Rubloff, Gary W. [4 ,5 ]
Bentley, William E. [1 ,2 ]
机构
[1] Univ Maryland, Fischell Dept Bioengn, College Pk, MD 20742 USA
[2] Univ Maryland, Biosystemat Res Ctr, Inst Biotechnol, College Pk, MD 20742 USA
[3] Univ Maryland, Dept Elect & Comp Engn, College Pk, MD 20742 USA
[4] Univ Maryland, ISR, College Pk, MD 20742 USA
[5] Univ Maryland, Dept Mat Sci & Engn, College Pk, MD 20742 USA
基金
美国国家科学基金会;
关键词
STREPTOCOCCAL PROTEIN-G; ESCHERICHIA-COLI; CHITOSAN; AUTOINDUCER-2; VIRULENCE; ENZYME; EXPRESSION; DEPOSITION; DESIGN; LUXS;
D O I
10.1039/b926846d
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
The emergence of bacteria that evade antibiotics has accelerated research on alternative approaches that do not target cell viability. One such approach targets cell-cell communication networks mediated by small molecule signaling. In this report, we assemble biological nanofactories within a bioMEMS device to capture and manipulate the behavior of quorum sensing (QS) bacteria as a step toward modifying small molecule signaling. Biological nanofactories are bio-inspired nanoscale constructs which can include modules with different functionalities, such as cell targeting, molecular sensing, product synthesis, and ultimately self-destruction. The biological nanofactories reported here consist of targeting, sensing, synthesis and, importantly, assembly modules. A bacteria-specific antibody constitutes the targeting module while a genetically engineered fusion protein contains the sensing, synthesis and assembly modules. The nanofactories are assembled on chitosan electrodeposited within a microchannel of the bioMEMS device; they capture QS bacteria in a spatially selective manner and locally synthesize and deliver the "universal" small signaling molecule autoinducer-2 (AI-2) at the captured cell surface. The nanofactory based AI-2 delivery is demonstrated to alter the progression of the native AI-2 based QS response of the captured bacteria. Prospects are envisioned for utilizing our technique as a test-bed for understanding the AI-2 based QS response of bacteria as a means for developing the next generation of antimicrobials.
引用
收藏
页码:1128 / 1134
页数:7
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