IP Library Granted Patent US 8,288,155
Granted Patent B2
US 8,288,155 · App. 11/777,919 · Granted Oct 16, 2012

Biomolecular attachment sites on microelectronic arrays and methods thereof

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Quick Facts
Patent No.
US 8,288,155
App. No.
11/777,919
Granted
Oct 16, 2012
Kind
B2
Abstract

Methods of addressing a biomolecule to a selectively addressable electrode are described. A permeation layer overlying a plurality of selectively addressable electrodes is provided. The permeation layer includes a reactive group that is adapted to bond to a biomolecule and that requires activation through a chemical transformation before bonding to the biomolecule. At least one selectively addressable electrode is biased such that a pH change occurs in an overlying solution of the at least one selectively addressable electrode. The reactive group in a portion of the permeation layer above the at least one selectively addressable electrode is then chemically transformed to an activated reactive group as a result of the pH change. A biomolecule is then bound to the permeation layer overlying the at least one selectively addressable electrode through the activated reactive group.

Claims (11)

1. A method of addressing a biomolecule to a selectively addressable electrode, comprising the steps of:

providing a permeation layer overlying a plurality of selectively addressable electrodes, the permeation layer comprising a reactive group adapted to bond to a biomolecule, wherein the reactive group requires activation through a chemical transformation before bonding to the biomolecule;

biasing at least one selectively addressable electrode such that a pH change occurs in an overlying solution of the at least one selectively addressable electrode, wherein the reactive group in a portion of the permeation layer above the at least one selectively addressable electrode is chemically transformed to an activated reactive group as a result of the pH change; and

binding a biomolecule to the permeation layer overlying the at least one selectively addressable electrode through the activated reactive group.

2. The method of claim 1 , wherein the reactive group is an acid labile group.

3. The method of claim 2 , wherein the acid labile group is selected from the group consisting of imines, TBOC, FMOC, trityl, trifluoroacetamide, and esters.

4. The method of claim 2 , wherein the reactive group is a thiol ester.

5. The method of claim 2 , wherein the reactive group is a ketal.

6. The method of claim 1 , wherein the biomolecule is covalently attached to the reactive group.

7. The method of claim 1 , wherein the biomolecule is a nucleic acid.

8. The method of claim 1 , wherein the biomolecule is selected from the group consisting of proteins, peptides, enzymes, and antibodies.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 1, 2019
From: GAMIDA FOR LIFE, B.V.
To: ADOR DIAGNOSTICS S.R.L.
Reel/Frame 048749/0393 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 19, 2010
From: ELITECH HOLDING B.V.
To: GAMIDA FOR LIFE B.V.
Reel/Frame 024260/0195 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2009
From: NANOGEN, INC.; EPOCH BIOSCIENCES, INC.; NANOTRONICS, INC.
To: ELITECH HOLDING B.V.
Reel/Frame 023004/0585 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 13, 2007
From: HAVENS, JOHN R.; ONOFREY, THOMAS J.; GREEF, CHARLES H.; KERVORKIAN, GREGORY J.; KROTZ, JAIN; LYKSTAD, KRISTIE L.; RAYMOND, DANIEL E.; REESE, HOWARD R.; ROONEY, REGINA; SCOTT, JOHN J.
To: NANOGEN, INC.
Reel/Frame 019557/0817 →