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一种用于革兰氏阳性菌成像的细胞膜荧光探针及实时跟踪细菌活力

A Cell Membrane Fluorogenic Probe for Gram-Positive Bacteria Imaging and Real-Time Tracking of Bacterial Viability.

机构信息

State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012, China.

CAS Key Laboratory of Separation Science for Analytical Chemistry, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, China.

出版信息

ACS Appl Bio Mater. 2021 Mar 15;4(3):2104-2112. doi: 10.1021/acsabm.0c01269. Epub 2020 Nov 11.

Abstract

Bacterial infections are a global healthcare problem, resulting in serious clinical morbidities and mortality. Real-time monitoring of live bacteria by fluorescent imaging technology has potential in diagnosis of bacterial infections, elucidating antimicrobial agents' mode of action, assessing drug toxicity, and examining bacterial antimicrobial resistance. In this work, a naphthalimide-derived fluorescent probe was developed for wash-free Gram-positive bacteria imaging. The probe aggregated in aqueous solutions and exhibited aggregation-caused fluorescence quenching (ACQ). The interaction with Gram-positive bacteria cell walls would selectively disaggregate the probe and the liberated probes were dispersed on the outside of the bacteria cell walls to achieve surface fluorescence imaging. There were no such interactions with Gram-negative bacteria, which indicates that selective binding and imaging of Gram-positive bacteria was achieved. The binding of zinc ions by can enhance the fluorescent signals on the bacterial surface by inhibiting the process of photoinduced electron transfer. complex was an excellent dye to discriminate mixed Gram-positive and Gram-negative bacteria. Also, live and dead bacteria can be differentially imaged by . Furthermore, was used for real-time monitoring bacteria viability such as treated with antibiotic vancomycin.

摘要

细菌感染是一个全球性的医疗保健问题,导致严重的临床发病率和死亡率。通过荧光成像技术实时监测活细菌在细菌感染的诊断、阐明抗菌剂的作用模式、评估药物毒性以及研究细菌抗菌耐药性方面具有潜在的应用价值。在这项工作中,开发了一种萘酰亚胺衍生的荧光探针 ,用于免洗革兰氏阳性细菌成像。探针在水溶液中聚集,并表现出聚集诱导的荧光猝灭(ACQ)。与革兰氏阳性细菌细胞壁的相互作用会选择性地使探针解聚,而释放的探针则分散在细菌细胞壁的外部,以实现表面荧光成像。与革兰氏阴性细菌没有这种相互作用,这表明实现了对革兰氏阳性细菌的选择性结合和成像。锌离子与 结合可以通过抑制光致电子转移过程来增强细菌表面的荧光信号。 配合物是一种极好的染料,可以区分混合的革兰氏阳性和革兰氏阴性细菌。此外, 还可以用于实时监测活菌和死菌,如用抗生素万古霉素处理的活菌和死菌。

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