posted on 2020-10-29, 20:13authored byZvi Yaari, Justin M. Cheung, Hanan A. Baker, Rune S. Frederiksen, Prakrit V. Jena, Christopher P. Horoszko, Fang Jiao, Simon Scheuring, Minkui Luo, Daniel A. Heller
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.