| Literature DB >> 33119310 |
Zvi Yaari1, Justin M Cheung1, Hanan A Baker1,2, Rune S Frederiksen1, Prakrit V Jena1, Christopher P Horoszko1,3, Fang Jiao2,4, Simon Scheuring2,4, Minkui Luo1,3, Daniel A Heller1,2,3.
Abstract
Enzymatic suicide inactivation, a route of permanent enzyme inhibition, is the mechanism of action for a wide array of pharmaceuticals. Here, we developed the first nanosensor that selectively reports the suicide inactivation pathway of an enzyme. The sensor is based on modulation of the near-infrared fluorescence of an enzyme-bound carbon nanotube. The nanosensor responded selectively to substrate-mediated suicide inactivation of the tyrosinase enzyme via bathochromic shifting of the nanotube emission wavelength. Mechanistic investigations revealed that singlet oxygen generated by the suicide inactivation pathway induced the response. We used the nanosensor to quantify the degree of enzymatic inactivation by measuring response rates to small molecule tyrosinase modulators. This work resulted in a new capability of interrogating a specific route of enzymatic death. Potential applications include drug screening and hit-validation for compounds that elicit or inhibit enzymatic inactivation and single-molecule measurements to assess population heterogeneity in enzyme activity.Entities:
Keywords: Drug development; Drug screening; Enzymology; High throughput assay; Reactive oxygen species
Year: 2020 PMID: 33119310 PMCID: PMC8177003 DOI: 10.1021/acs.nanolett.0c01858
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189