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结构性质决定金黄色葡萄球菌选择性光示踪剂检测。

Structural Properties Dictating Selective Optotracer Detection of Staphylococcus aureus.

机构信息

AIMES - Center for the Advancement of Integrated Medical, and Engineering Sciences, Karolinska Institutet and KTH Royal Institute of Technology, Solnavägen 9, 171 77, Stockholm, Sweden.

Department of Neuroscience, Karolinska Institutet, Solnavägen 9, 171 77, Stockholm, Sweden.

出版信息

Chembiochem. 2022 Jun 3;23(11):e202100684. doi: 10.1002/cbic.202100684. Epub 2022 Apr 1.

Abstract

Optotracers are conformation-sensitive fluorescent tracer molecules that detect peptide- and carbohydrate-based biopolymers. Their binding to bacterial cell walls allows selective detection and visualisation of Staphylococcus aureus (S. aureus). Here, we investigated the structural properties providing optimal detection of S. aureus. We quantified spectral shifts and fluorescence intensity in mixes of bacteria and optotracers, using automatic peak analysis, cross-correlation, and area-under-curve analysis. We found that the length of the conjugated backbone and the number of charged groups, but not their distribution, are important factors for selective detection of S. aureus. The photophysical properties of optotracers were greatly improved by incorporating a donor-acceptor-donor (D-A-D)-type motif in the conjugated backbone. With significantly reduced background and binding-induced on-switch of fluorescence, these optotracers enabled real-time recordings of S. aureus growth. Collectively, this demonstrates that chemical structure and photophysics are key tunable characteristics in the development of optotracers for selective detection of bacterial species.

摘要

光追踪剂是构象敏感的荧光示踪分子,可检测基于肽和碳水化合物的生物聚合物。它们与细菌细胞壁的结合允许选择性检测和可视化金黄色葡萄球菌(S. aureus)。在这里,我们研究了提供最佳 S. aureus 检测的结构特性。我们使用自动峰分析、互相关和曲线下面积分析来量化细菌和光追踪剂混合物中的光谱位移和荧光强度。我们发现,共轭主链的长度和带电荷基团的数量,而不是它们的分布,是选择性检测 S. aureus 的重要因素。通过在共轭主链中引入供体-受体-供体(D-A-D)型结构单元,光追踪剂的光物理性质得到了极大的改善。由于背景显著降低,并且结合诱导的荧光开/关,这些光追踪剂能够实时记录 S. aureus 的生长。总的来说,这表明化学结构和光物理性质是开发用于选择性检测细菌种类的光追踪剂的关键可调特性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ee8/9400997/c77d6c7e6d81/CBIC-23-0-g003.jpg

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