Smart glass slide for microarrays

• US 10,379,117 B2
• Filed: 10/18/2017
• Issued: 08/13/2019
• Est. Priority Date: 03/15/2013
• Status: Active Grant

• Current Assignee: Robert Bosch GmbH
• Original Assignee: Robert Bosch GmbH
• Inventors: Fomina, Nadezda, Johnson, Christopher, Kavusi, Sam, Ahmad, Habib
• Primary Examiner(s): Bunker, Amy M
• Application Number:
  US15/787,523
• Publication Number:
  US 20180038851A1
• Time in Patent Office: 664 Days
• CPC Class Codes: G01N 27/3272 Test elements therefor, i.e. disposable laminated substrates with electrodes, reagent and channels optical biosensors G01N33/52
• CPC Class Codes: G01N 33/5438 Electrodes

Abstract

Device for use in a biosensor comprising a multisite array of test sites, the device being useful for modulating the binding interactions between a (biomolecular) probe or detection agent and an analyte of interest from a biological by modulating the pH or ionic gradient near the electrodes in such biosensor. The device provides a biosensor which is more accurate, reliable and the results of which are more reproducible. Analytic methods for more accurately measuring an analyte of interest in a biological sample are also provided.

Claims

1. A method for detecting a biomolecule analyte in a biological sample, the method comprising:

(a) adding a dilute phosphate buffer and an electrochemically active agent to an aqueous solution of each test site in a multisite array of test sites in a biosensor, wherein conditions for interacting with the biomolecule analyte at each of the test sites can be varied independently;

(b) electrochemically reacting the electrochemically active agent in the aqueous solution at each test site through one or more electrodes supported on a glass or plastic support substrate to produce hydrogen ions (H⁺) or hydroxide ions (OH⁻

), thereby modulating and controlling the pH at each test site;

(c) adding a biological sample to the aqueous solution of each of the test sites, wherein;

each of the test sites includes a biomolecular interface layer that includes;

(i) a layer of immobilized polymer that covers the glass or plastic support substrate;

(ii) one or more pH sensitive fluorescent proteins immobilized by attachment directly to the layer of immobilized polymer; and

(iii) one or more probes immobilized by attachment directly to the layer of immobilized polymer;

a first portion of the one or more pH sensitive fluorescent proteins is located within a maximum distance from the one or more electrodes within which the one or more electrodes is able to affect pH of the one or more pH sensitive fluorescent proteins; and

a second portion of the one or more pH sensitive fluorescent proteins is located more than the maximum distance from the one or more electrodes;

(d) determining the pH at each of the test sites using a fluorescence intensity of the one or more pH sensitive fluorescent proteins; and

(e) detecting the biomolecule analyte in each of the test sites;

wherein;

amounts of the electrochemically active agent and the electrochemical reaction are varied between the test sites in a subset of the array of test sites in order to obtain sets of test sites in which the pH or ionic concentration at the one or more electrode surfaces in the test sites varies to produce a pH or ionic concentration gradient at the one or more electrodes and in a vicinity of the one or more probes in the biomolecular interface layer; and

the one or more pH sensitive fluorescent proteins is one or more Green Fluorescent Proteins.

2. The method of claim 1, wherein the second portion of the one or more pH sensitive fluorescent proteins is used as an internal reference for signal normalization.