2020
DOI: 10.1002/anie.201915783
|View full text |Cite
|
Sign up to set email alerts
|

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

Abstract: 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… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
16
0

Year Published

2020
2020
2024
2024

Publication Types

Select...
8
1

Relationship

1
8

Authors

Journals

citations
Cited by 40 publications
(20 citation statements)
references
References 46 publications
0
16
0
Order By: Relevance
“…Due to the insolubility of C 70 in water and water‐miscible solvents, standard methodologies for determining binding energy, such as ITC or fluorescence titration analysis, [ 67 ] cannot be performed for C 70 and lysozyme. Nevertheless, we determined the binding affinity between the two interacting systems using a computational protocol, which was recently validated to calculate the binding energy between proteins and fullerenes (Section S7, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Due to the insolubility of C 70 in water and water‐miscible solvents, standard methodologies for determining binding energy, such as ITC or fluorescence titration analysis, [ 67 ] cannot be performed for C 70 and lysozyme. Nevertheless, we determined the binding affinity between the two interacting systems using a computational protocol, which was recently validated to calculate the binding energy between proteins and fullerenes (Section S7, Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…34 ). 136 The inhibitor ethylmalonic acid was used as the targeting moiety to deliver the probe into the cavity of CK-B, and TPE was used as the fluorophore. When probe 46 was inserted into the cavity of CK-B, the molecular motion of TPE was restricted, and TPE emitted strong fluorescence.…”
Section: Fluorescent Probes For Ros-associated Proteins In Diseasesmentioning
confidence: 99%
“…There are a wide array of instrumental methods allowing identification and determination of various metal elements in different evidences, such as atomic absorption spectroscopy, neutron activation analysis, X-ray fluorescence spectroscopy, ion chromatography, mass spectroscopy, and other spectroscopy coupled with mass spectroscopy (Ulrich et al, 2004;Verma, 2018;Sliwińska et al, 2019). Compared with these traditional analytical methods, fluorescence spectroscopy is more suitable for trace metal ions analysis in complex matrices because of its short response time, simplicity, high selectivity, and sensitivity (Fu et al, 2019;Zhang et al, 2019;Niu et al, 2020;Zang et al, 2020).…”
Section: Introductionmentioning
confidence: 99%