IP Library Granted Patent US 9,846,154
Granted Patent B2
US 9,846,154 · App. 14/366,597 · Granted Dec 19, 2017

Optical method and device for identifying and quantifying analytes

Inventors: Guillaume Suárez (Lussery-Villars, CH); Christian Santschi (Lausanne, CH); Olivier Martin (Pully, CH)
Assignee: Ecole Polytechnique Fédérale de Lausanne (EPFL)
G01N33/573C12Q1/26G01N21/314
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,846,154
App. No.
14/366,597
Granted
Dec 19, 2017
Kind
B2
Abstract

A method for analyzing a metalloprotein and/or the interaction with its environment comprising the following steps: (a) Providing a medium that enhances the detection of the electromagnetic cross-section signal of metalloproteins, (b) Incorporating a metalloprotein to analyse into said medium, (c) Contacting said medium with electromagnetic radiation, (d) Obtaining the electromagnetic cross-section spectrum of said metalloprotein, (e) Determining from said electromagnetic cross-section spectrum at least one parameter related to one or several analytes of interest.

Claims (17)

1. A method for analyzing an analyte comprising the steps of:

(a) providing a multiscattering medium that enhances a detection of an electromagnetic cross-section signal of a metalloprotein,

(b) incorporating the metalloprotein to be analyzed into the multiscattering medium and the analyte is arranged to establish a redox reaction with the metalloprotein,

(c) contacting the multiscattering medium with electromagnetic radiation,

(d) obtaining the electromagnetic cross-section spectrum of the metalloprotein, and

(e) determining from the electromagnetic cross-section spectrum a concentration of the analyte.

2. The method according to claim 1 wherein the electromagnetic cross-section is an absorption cross-section of the metalloprotein.

3. The method according to claim 1 wherein the multiscattering medium is at least one of an aggregate; a suspension; a gel; a porous membrane; a microstructured substrate; and a nanostructured substrate.

4. The method according to claim 1 wherein the analyte is a reaction product of enzymatic or chemical reactions.

5. The method according to claim 1 wherein the step of (c) contacting uses a dark-field electromagnetic radiation illumination.

6. The method according to claim 1 wherein the step of (e) determining further includes:

determining the concentration of the analyte based on a measurement of a molecular state of the metalloprotein.

7. The method according to claim 6 wherein the molecular state is an oxidation state.

8. The method according to claim 1 wherein the analyte is hydrogen peroxide.

9. The method according to claim 1 wherein the metalloprotein is a cytochrome c.

10. The method according to claim 1 , wherein the multiscattering medium enhances an optical cross-section of the metalloprotein.

11. The method according to claim 1 , wherein the multiscattering medium provides for an amplification of the electromagnetic cross-section spectrum to suppress a background signal.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 10, 2014
From: SUAREZ, GUILLAUME; SANTSCHI, CHRISTIAN; MARTIN, OLIVIER
To: ECOLE POLYTECHNIQUE FEDERALE DE LAUSANNE (EPFL)
Reel/Frame 033281/0657 →
Priority Claims (1)
WO PCT/IB2011/055819 · Dec 20, 2011 · international
Continuity (1)
Related Publication 20140322733A1 · Oct 30, 2014