Y10T436/18

Self-immolative probes for enzyme activity detection

Provided is a compound having the structure: (SIG)-(SI-MOD).sub.m
where SIG is a signaling molecule, SI is a self-immolative structure bound to SIG such that SIG has a reduced signal relative to the signal of SIG without SI, MOD is a moiety bound to SI that is subject to modification by an activator, and m is an integer from 1 to about 10. When MOD is modified by an activator, SI is destabilized and self-cleaved from SIG such that SIG generates an increased signal. Also provided are methods of determining whether a sample, such as a cell, comprises an activator, such as a nitroreducase, using the compound. Further provided are methods of determining whether a mammalian cell is hypoxic using the compound where nitroreductase is the activator. A method of detecting a microorganism that comprises a nitroreductase using the compound where nitroreductase is the activator is also provided.

SELF-IMMOLATIVE PROBES FOR ENZYME ACTIVITY DETECTION

Provided is a compound comprising the structure:


(SIG)-(SI-MOD).sub.m.

In this compound, SIG is a signaling molecule, SI is a self-immolative structure bound to SIG such that SIG has a reduced signal relative to the signal of SIG without SI, MOD is a moiety bound to SI that is subject to modification by an activator, and m is an integer from 1 to about 10. With this compound, when MOD is modified by an activator, SI is destabilized and self-cleaved from SIG such that SIG generates an increased signal. Also provided is a method of determining whether a sample comprises an activator, using the above-described compound. Additionally provided is a method of determining whether a cell comprises a nitroreductase using the above-described compound where nitroreductase is the activator. Further provided is a method of determining whether a mammalian cell is hypoxic using the above-described compound where nitroreductase is the activator. A method of detecting a microorganism that comprises a nitroreductase, using the above-described compound where nitroreductase is the activator, is also provided. Also provided is a method of identifying nitroreductase in a sample, using the above-described compound where nitroreductase is the activator.

Fluorescent method to quantify copper or platinum based on catalysis

Methods of detecting platinum and copper in a test sample are provided. Kits for use in detecting platinum and copper in a test sample also are provided.

Ultra low range sulfite measurement
11231368 · 2022-01-25 · ·

An embodiment provides a method for measuring sulfite in a solution, including: preparing a hemicyanine indicator; introducing the hemicyanine indicator to a solution containing an amount of sulfite, wherein the hemicyanine indicator reacts with the sulfite and causes a change in fluorescence of the solution; and measuring the amount of sulfite in the solution by measuring an intensity of the fluorescence. Other aspects are described and claimed.

Fluorescent method to quantify copper or platinum based on catalysis

Methods of detecting platinum and copper in a test sample are provided. Kits for use in detecting platinum and copper in a test sample also are provided.

Fluorescent Method to Quantify Copper or Platinum Based on Catalysis
20220260493 · 2022-08-18 ·

Methods of detecting platinum and copper in a test sample are provided. Kits for use in detecting platinum and copper in a test sample also are provided.

COMPOSITIONS AND METHODS FOR DIAGNOSIS OF SHOCK
20210139946 · 2021-05-13 ·

Methods and kits for diagnosis and staging of shock, and especially non-septic shock are presented in which protease activities and/or volatile compounds are measured from a biological sample to so identify and/or stage shock.

ULTRA LOW RANGE SULFITE MEASUREMENT
20200378893 · 2020-12-03 ·

An embodiment provides a method for measuring sulfite in a solution, including: preparing a hemicyanine indicator; introducing the hemicyanine indicator to a solution containing an amount of sulfite, wherein the hemicyanine indicator reacts with the sulfite and causes a change in fluorescence of the solution; and measuring the amount of sulfite in the solution by measuring an intensity of the fluorescence. Other aspects are described and claimed.

SELF-IMMOLATIVE PROBES FOR ENZYME ACTIVITY DETECTION

Provided is a compound having the structure:


(SIG)-(SI-MOD).sub.m

where SIG is a signaling molecule, SI is a self-immolative structure bound to SIG such that SIG has a reduced signal relative to the signal of SIG without SI, MOD is a moiety bound to SI that is subject to modification by an activator, and m is an integer from 1 to about 10. When MOD is modified by an activator, SI is destabilized and self-cleaved from SIG such that SIG generates an increased signal. Also provided are methods of determining whether a sample, such as a cell, comprises an activator, such as a nitroreducase, using the compound. Further provided are methods of determining whether a mammalian cell is hypoxic using the compound where nitroreductase is the activator. A method of detecting a microorganism that comprises a nitroreductase using the compound where nitroreductase is the activator is also provided.

Self-immolative probes for enzyme activity detection

Provided is a compound having the structure:
(SIG)-(SI-MOD).sub.m
where SIG is a signaling molecule, SI is a self-immolative structure bound to SIG such that SIG has a reduced signal relative to the signal of SIG without SI, MOD is a moiety bound to SI that is subject to modification by an activator, and m is an integer from 1 to about 10. When MOD is modified by an activator, SI is destabilized and self-cleaved from SIG such that SIG generates an increased signal. Also provided are methods of determining whether a sample, such as a cell, comprises an activator, such as a nitroreducase, using the compound. Further provided are methods of determining whether a mammalian cell is hypoxic using the compound where nitroreductase is the activator. A method of detecting a microorganism that comprises a nitroreductase using the compound where nitroreductase is the activator is also provided.