纳米团簇
材料科学
对映体
圆二色性
分子识别
纳米技术
纳米材料
配体(生物化学)
手性(物理)
齿合度
对映选择合成
纳米颗粒
组合化学
肽
八面体
对映体过量
立体中心
化学
作者
Xuejuan Wang,Xiangyang Zhang,Yue Zhao,Xirui Wu,Guangbao Yang,Yanli Zhao,Guofeng Liu
标识
DOI:10.1002/adma.202514158
摘要
Abstract The biomimetic chiral recognition and detection of biothiols, such as cysteine, homocysteine, and glutathione, in plasma present significant challenges due to the limited understanding of chiral recognition mechanisms beyond the molecular level. Herein, enantiomeric and twisted octahedron silver nanoclusters (D‐/L‐Ag 6 SP 6 ), featuring bichirality at both the molecular and nanoscopic scales, are designed and synthesized by employing a chiral bidentate ligand of thiazolethione enantiomer (D‐ or L‐4‐phenylthiazolidine‐2‐thione, abbreviated as D‐SP or L‐SP) in conjunction with silver acetate. The resulting nanoclusters are further modified with PEG 2000 to produce water‐dispersible D‐Ag 6 SP 6 @PEG and L‐Ag 6 SP 6 @PEG nanoparticles, enabling enantioselective recognition and quantitative determination of various biothiols in plasma through circular dichroism measurements. The study also elucidates the bichiral recognition and determination of biothiols through a ligand‐induced disassembly‐assembly mechanism. Both D‐ and L‐type Ag 6 SP 6 @PEG nanoparticles demonstrate excellent anti‐interference properties for discriminating biothiols using principal component analysis. The bichirality of nanoclusters shows high enantioselectivity in chiral recognition of biothiols and their corresponding enantiomers. This work not only provides a convenient strategy for bichiral recognition and quantitative determination of biothiols in plasma, but also holds promise for developing hierarchically chiral nanomaterials applicable in biomedical engineering, nanomedicine, and drug screening.
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