化学
纳米团簇
金黄色葡萄球菌
生物物理学
肽
衍射
细胞质
相干衍射成像
纳米颗粒
细菌
纳米技术
生物化学
光学
物理
数学分析
有机化学
傅里叶变换
生物
材料科学
相位恢复
遗传学
数学
作者
Tangmeng Li,Bo He,Xiangchun Zhang,Jiadong Fan,Liang Gao,Zhibin Sun,Jian‐Hua Zhang,Amin Guo,Dan Pan,Xianzhen Yin,Yajun Tong,Changyong Song,Yoshiki Kohmura,Makina Yabashi,Tetsuya Ishikawa,Xueyun Gao,Huaidong Jiang
出处
期刊:Analytical Chemistry
[American Chemical Society]
日期:2022-09-16
卷期号:94 (38): 13136-13144
被引量:11
标识
DOI:10.1021/acs.analchem.2c02638
摘要
Characterizing interactions between microbial cells and their specific inhibitory drugs is essential for developing effective drugs and understanding the therapeutic mechanism. Functional metal nanoclusters can be effective inhibitory agents against microorganisms according to various characterization methods, but quantitative three-dimensional (3D) spatial structural analysis of intact cells is lacking. Herein, using coherent X-ray diffraction imaging, we performed in situ 3D visualization of unstained Staphylococcus aureus cells treated with peptide-mineralized Au-cluster probes at a resolution of ∼47 nm. Subsequent 3D mass-density mapping and quantitative structural analyses of S. aureus in different degrees of destruction showed that the bacterial cell wall was damaged and cytoplasmic constituents were released from cells, confirming the significant antibacterial effects of the Au-cluster probe. This study provides a promising nondestructive approach for quantitative imaging and paves the way for further research into microbe-inhibitor drug interactions.
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