Lim Yong-beom, Park Somi, Lee Eunji, Ryu Ja-Hyoung, Yoon You-Rim, Kim Tae-Hyun, Lee Myongsoo
Center for Supramolecular Nano-Assembly, Department of Chemistry, Yonsei University, Seoul 120-749, Korea.
Chem Asian J. 2007 Nov 5;2(11):1363-9. doi: 10.1002/asia.200700163.
We explored a method of controlling bacterial motility and agglutination by using self-assembled carbohydrate-coated beta-sheet nanoribbons. To this aim, we synthesized triblock peptides that consist of a carbohydrate, a polyethylene glycol (PEG) spacer, and a beta-sheet-forming peptide. An investigation into the effect of PEG-spacer length on the self-assembly of the triblock peptides showed that the PEG should be of sufficiently length to stabilize the beta-sheet nanoribbon structure. It was found that the stabilization of the nanoribbon led to stronger activity in bacterial motility inhibition and agglutination, thus suggesting that antibacterial activity can be controlled by the stabilization strategy. Furthermore, another level of control over bacterial motility and agglutination was attained by co-assembly of bacteria-specific and -nonspecific supramolecular building blocks. The nanoribbon specifically detected bacteria after the encapsulation of a fluorescent probe. Moreover, the detection sensitivity was enhanced by the formation of bacterial clusters. All these results suggest that the carbohydrate-coated beta-sheet nanoribbons can be developed as promising agents for pathogen capture, inactivation, and detection, and that the activity can be controlled at will.
我们探索了一种通过使用自组装的碳水化合物包被的β-折叠纳米带控制细菌运动性和凝集的方法。为此,我们合成了由碳水化合物、聚乙二醇(PEG)间隔区和β-折叠形成肽组成的三嵌段肽。对PEG间隔区长度对三嵌段肽自组装的影响的研究表明,PEG应有足够的长度来稳定β-折叠纳米带结构。发现纳米带的稳定导致细菌运动抑制和凝集方面更强的活性,因此表明抗菌活性可以通过稳定策略来控制。此外,通过细菌特异性和非特异性超分子构建块的共组装实现了对细菌运动性和凝集的另一级控制。在包封荧光探针后,纳米带特异性地检测到细菌。此外,细菌簇的形成提高了检测灵敏度。所有这些结果表明,碳水化合物包被的β-折叠纳米带可被开发成为用于病原体捕获、灭活和检测的有前景的试剂,并且其活性可以随意控制。