Lee Taeksu, Lim Jaewoo, Park Kyoungsook, Lim Eun-Kyung, Lee Jae-Jong
Department of Nano Manufacturing Technology, Korea Institute of Machinery and Materials (KIMM), 156 Gajeongbuk-Ro, Yuseong-Gu, Daejeon 34103, Republic of Korea.
Bionano Technology Research Center, Korea Research Institute of Bioscience and Biotechnology (KRIBB), 125 Gwahak-ro, Yuseong-gu, Daejeon 34141, South Korea.
ACS Sens. 2020 Oct 23;5(10):3099-3108. doi: 10.1021/acssensors.0c01139. Epub 2020 Aug 21.
Biological metamaterials with a specific size and spacing are necessary for developing highly sensitive and selective sensing systems to detect hazardous bacteria in complex solutions. Herein, the construction of peptidoglycan-binding protein (PGBP)-based metamaterials to selectively capture Gram-positive cells with high efficacy is reported. Nanoimprint lithography was used to generate a nanohole pattern as a template, the inside of which was modified with nickel(II)-nitrilotriacetic acid (Ni-NTA). Then, PGBP metamaterials were fabricated by immobilizing PGBP via chelation between Ni-NTA and six histidines on PGBP. Compared to the flat and spread PGBP-covered bare substrates, the PGBP-based metamaterials enabled selective capturing of Gram-positive bacteria with high efficacy, owing to enhanced interactions between the metamaterials and bacterial surface not shown in bulk materials. Thereafter, the specific strain and quantitative information of the captured bacteria was obtained by surface-enhanced Raman scattering mapping analysis in the 1 to 1 × 10 cfu/mL range within 30 min. It should be noted that no additional signal amplification process was required for lowly abundant bacteria, even at the single-bacterium level. The PGBP-based metamaterials could be regenerated multiple times with preserved sensing efficiency. Finally, this assay can detect specific Gram-positive bacteria, such as , in human plasma.
具有特定尺寸和间距的生物超材料对于开发高灵敏度和选择性的传感系统以检测复杂溶液中的有害细菌至关重要。在此,报道了基于肽聚糖结合蛋白(PGBP)的超材料的构建,以高效地选择性捕获革兰氏阳性细胞。纳米压印光刻用于生成纳米孔图案作为模板,其内部用镍(II)-次氮基三乙酸(Ni-NTA)进行修饰。然后,通过Ni-NTA与PGBP上的六个组氨酸之间的螯合固定PGBP来制备PGBP超材料。与平坦且铺展有PGBP的裸基板相比,基于PGBP的超材料能够高效地选择性捕获革兰氏阳性细菌,这是由于超材料与细菌表面之间的相互作用增强,而在块状材料中未观察到这种相互作用。此后,通过表面增强拉曼散射映射分析在30分钟内在1至1×10 cfu/mL范围内获得捕获细菌的特定菌株和定量信息。需要注意的是,即使对于低丰度细菌,甚至在单细菌水平,也不需要额外的信号放大过程。基于PGBP的超材料可以多次再生并保持传感效率。最后,该检测方法可以检测人血浆中的特定革兰氏阳性细菌,例如 。