Memorial Sloan Kettering Cancer Center, New York, New York 10065, United States.
Department of Physiology and Biophysics, Weill Cornell Medicine, 1300 York Avenue, New York, New York 10065, United States.
Nano Lett. 2020 Nov 11;20(11):7819-7827. doi: 10.1021/acs.nanolett.0c01858. Epub 2020 Oct 29.
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.
酶促自杀失活是一种广泛应用于各类药物的永久酶抑制机制。在此,我们开发了首个纳米传感器,可选择性报告酶的自杀失活途径。该传感器基于对结合酶的碳纳米管近红外荧光的调制。纳米传感器通过纳米管发射波长的红移,对酪氨酸酶的底物介导自杀失活反应进行了选择性响应。机理研究表明,自杀失活途径产生的单线态氧诱导了这一响应。我们使用纳米传感器通过测量小分子酪氨酸酶调节剂的响应速率,定量测定酶失活的程度。这项工作为研究特定的酶死亡途径提供了新的能力。潜在的应用包括药物筛选和针对引发或抑制酶失活化合物的验证,以及用于评估酶活性的群体异质性的单分子测量。