Noncovalent Chirality Sensing Ensembles for the Detection and Reaction Monitoring of Amino Acids, Peptides, Proteins, and Aromatic Drugs

被引:191
|
作者
Biedermann, Frank [1 ]
Nau, Werner M. [1 ]
机构
[1] Jacobs Univ Bremen, Sch Sci & Engn, D-28759 Bremen, Germany
关键词
circular dichroism; cucurbiturils; dyes; macrocycles; sequence recognition; supramolecular chemistry; INDUCED CIRCULAR-DICHROISM; TANDEM ENZYME ASSAYS; CHARGE-TRANSFER COMPLEXES; ENANTIOMERIC EXCESS; MOLECULAR RECOGNITION; SECONDARY ALCOHOLS; HOST; CUCURBITURIL; CYCLODEXTRIN; DISPLACEMENT;
D O I
10.1002/anie.201400718
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ternary complexes between the macrocyclic host cucurbit[8]uril, dicationic dyes, and chiral aromatic analytes afford strong induced circular dichroism (ICD) signals in the near-UV and visible regions. This allows for chirality sensing and peptide-sequence recognition in water at low micromolar analyte concentrations. The reversible and noncovalent mode of binding ensures an immediate response to concentration changes, which allows the real-time monitoring of chemical reactions. The introduced supramolecular method is likely to find applications in bioanalytical chemistry, especially enzyme assays, for drug-related analytical applications, and for continuous monitoring of enantioselective reactions, particularly asymmetric catalysis.
引用
收藏
页码:5694 / 5699
页数:6
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