IP Library Granted Patent US 7,445,887
Granted Patent B2
US 7,445,887 · App. 11/326,689 · Granted Nov 4, 2008

Enzyme activity measurements using bio-layer interferometry

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Quick Facts
Patent No.
US 7,445,887
App. No.
11/326,689
Granted
Nov 4, 2008
Kind
B2
Abstract

Disclosed are enzyme assays using biolayer interferometry. Assays may be carried out using immobilized substrate or with a substrate capture format. In certain embodiments, the assays are carried out using unlabeled substrates. The methods are broadly applicable to enzyme assay measurements, can be carried out in vivo or in vitro, and are easily multiplexed.

Claims (24)

1. A method for assaying enzyme activity, comprising:

providing an optical element coupled to a light source via a mechanical coupling that engages the optical element with an optical fiber and provides an air gap between the optical element and the fiber, the optical element including (a) a proximal reflecting surface and a distal reflecting surface separated by at least 50 nm, and (b) a layer of enzyme substrate molecules positioned so that interference between a reflected beam from the proximal reflecting surface and a reflected beam from the distal reflecting surface varies as an enzyme reacts with the substrate, and wherein the reflected beams are coupled into the optical fiber;

exposing the optical element to an enzyme; and

detecting a change in the interference between the reflected beams, wherein the change is indicative of enzyme activity.

2. The method of claim 1 , wherein the enzyme is a hydrolase or a transferase.

3. The method of claim 2 , wherein the enzyme is a protease, a phosphatase, a glycosylase, or an esterase.

4. The method of claim 2 , wherein the enzyme is a nucleotide transferase, a glycosyl transferase or a phosphotransferase.

5. The method of claim 1 , further comprising providing a second optical element coupled to the light source via a second fiber, the second optical element including (c) a proximal reflecting surface and a distal reflecting surface separated by at least 50 nm, and (d) a layer of enzyme binding molecules positioned so that interference between a second reflected beam from the second optical element proximal reflecting surface and a reflected beam from the second optical element distal reflecting surface varies as the enzyme binds to the layer of enzyme binding molecules, and wherein the second reflected beams are coupled into the fiber; and detecting a change in the interference between the second reflected beams, wherein the change is indicative of enzyme activity.

6. The method of claim 5 , wherein the layer of enzyme binding molecules comprises an anti-enzyme antibody, a fragment of an anti-enzyme antibody, or an anti-enzyme scFv molecule.

7. The method of claim 1 , wherein the optical element is a first optical element, and wherein the method further comprises providing a second optical element positioned between the proximal reflecting surface of the first optical element and the fiber, the second optical element being coupled to the light source via the mechanical coupling that engages the second optical element with the fiber and provides an air gap between the second optical element and the fiber, and wherein the first optical element is coupled to the second optical element at the proximal reflective surface.

8. A method for assaying enzyme activity, comprising:

providing an optical element coupled to a light source via a mechanical coupling that engages the first optical element with a fiber and provides an air gap between the first optical element and the fiber, the optical element including (a) a proximal reflecting surface and a distal reflecting surface separated by at least 50 nm, and (b) a layer of analyte binding molecules;

exposing the optical element to an enzyme substrate reacted or reacting with an enzyme, whereby the enzyme substrate or a portion of the enzyme substrate binds to the layer of analyte binding molecules, and wherein interference between a reflected beam from the proximal reflecting surface and a reflected beam from the distal reflecting surface varies as the enzyme substrate or portion thereof binds to the layer of enzyme binding molecules, the reflected beams coupled into the fiber; and

detecting a change in optical thickness of the first reflecting surface, wherein the change is indicative of enzyme activity.

9. The method of claim 8 , wherein the enzyme is a hydrolase or a transferase.

10. The method of claim 9 , wherein the enzyme is a protease, a phosphatase, a glycosylase, or an esterase.

11. The method of claim 9 , wherein the enzyme is a nucleotide transferase, a glycosyl transferase or a phosphotransferase.

12. The method of claim 8 , further comprising interposing a semi-permeable membrane between said optical element and said substrate.

13. The method of claim 8 , wherein said substrate is bound to a support.

14. The method of claim 8 , further comprising providing a second optical element coupled to the light source via a second fiber, the second optical element including (c) a proximal reflecting surface and a distal reflecting surface separated by at least 50 nm, and (d) a layer of enzyme binding molecules positioned so that interference between a second reflected beam from the second optical element proximal reflecting surface and a reflected beam from the second optical element distal reflecting surface varies as the enzyme binds to the layer of enzyme binding molecules, and wherein the second reflected beams are coupled into the fiber; and detecting a change in the interference between the second reflected beams, wherein the change is indicative of enzyme activity.

15. The method of claim 14 , wherein the layer of enzyme binding molecules comprises an anti-enzyme antibody, a fragment of an anti-enzyme antibody, or an anti-enzyme scFv molecule.

16. The method of claim 8 , wherein the layer of analyte binding molecules comprises avidin, streptavidin, biotin, an antibody, an antibody fragment, an scFv, or a lectin.

17. The method of claim 8 , further comprising the step of inactivating the enzyme before the exposing step.

18. The method of claim 8 , wherein the optical element is a first optical element, and wherein the method further comprises providing a second optical element positioned between the proximal reflecting surface of the first optical element and the fiber, the second optical element being coupled to the light source via the mechanical coupling that engages the second optical element with the fiber and provides an air gap between the second optical element and the fiber, and wherein the first optical element is coupled to the second optical element at the proximal reflective surface.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 14, 2020
From: MOLECULAR DEVICES, LLC
To: SARTORIUS BIOANALYTICAL INSTRUMENTS, INC.
Reel/Frame 052659/0539 →
MERGER Recorded Feb 1, 2019
From: PALL FORTEBIO LLC
To: MOLECULAR DEVICES, LLC
Reel/Frame 048220/0165 →
CHANGE OF NAME Recorded Feb 1, 2019
From: PALL FORTE BIO CORP.
To: PALL FORTEBIO LLC
Reel/Frame 048228/0451 →
MERGER Recorded Jun 8, 2012
From: FORTEBIO, INC.; PROJECT PHOENIX ACQUISITION CORP.
To: PALL FORTEBIO CORP.
Reel/Frame 028345/0275 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 6, 2006
From: ZUK, ROBERT; CHOO, SAE; MA, WEILEI; WITTE, KRISTA
To: FORTEBIO, INC.
Reel/Frame 017452/0524 →