4.8 Article

In Vitro Light-Up Visualization of a Subunit-Specific Enzyme by an AIE Probe via Restriction of Single Molecular Motion

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 59, 期 25, 页码 10003-10007

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201915783

关键词

aggregation-induced emission; creatine kinase isoenzyme; fluorescence imaging; fluorescent probes

资金

  1. National Natural Science Foundation of China [21575015, 21505004, 20974009]
  2. Special Fund of Taishan Scholars Project of Shandong Province, China [tsqn201909012]

向作者/读者索取更多资源

Enzymes contain several subunits to maintain different biological functions. However, it remains a great challenge for specific discrimination of one subunit over another. Toward this end, the fluorescent probe TPEMA is now presented for highly specific detection of the B subunit of cytosolic creatine (CK) kinase isoenzyme (CK-B). Owing to its aggregation-induced emission property, TPEMA shows highly boosted emission toward CK-B with a fast response time and very low interference from other analytes, including the M subunit of CK (CK-M). With the aid of a Job plot assay, ITC assay and molecular dynamics simulation, it was directly confirmed that the remarkably enhanced fluorescence of TPEMA in the presence of CK-B results from the restriction of single molecular motion in the cavity. Selective wash-free fluorescence imaging of CK-B in macrophages under different treatments was successfully demonstrated.

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