Methods for detecting interaction of molecules with surface-bound reagents

• US 20020102596A1
• Filed: 01/31/2002
• Published: 08/01/2002
• Est. Priority Date: 01/31/2001
• Status: Abandoned Application

• Current Assignee: University of Tennessee Research Foundation (University of Teesside)
• Original Assignee: University of Tennessee Research Foundation (University of Teesside)
• Inventors: Davis, Lloyd Mervyn
• Application Number:
  US10/066,074
• Publication Number:
  US 20020102596A1
• Time in Patent Office: Days
• US Class Current: 435/6
• CPC Class Codes: C12Q 1/6823 Release of bound markers
• CPC Class Codes: C12Q 2525/117 incorporating modified base
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2565/601 being a microscope, e.g. atomic force microscopy [AFM]
• CPC Class Codes: Y10T 436/13 Tracers or tags

Abstract

Methods and devices for detecting the interaction of single molecules with surface-bound reagents are disclosed. The methods utilize synchronized techniques for controlling the interaction between labeled molecules in a flowing solution with reagents supported on a surface, and incorporate optical detection techniques such as fluorescence measurements. One application of the disclosed methods and devices is the detection of chemical reactions in which the nucleobases of labeled NTP molecules become incorporated into the DNA of a surface-bound enzyme-DNA complex with release of the labels.

Claims

1. A method for optically detecting labeled molecules that have participated in a chemical reaction with a reagent supported on a surface, comprising:

a) providing a flow cell;

b) providing within said flow cell a solid support having a surface;

c) supporting at least one reagent molecule to said surface;

d) introducing at least two flowing solutions into said flow cell, wherein at least one solution comprises a labeled molecule that can contact said reagent molecule, and at least one solution comprises buffer with no detectable labels, and wherein the at least two solutions are at different locations within the flow cell at any time;

e) immersing the supported reagent in a solution comprising labeled molecules;

f) switching or directing the flowing solutions with respect to the supported reagent, or switching the location of the supported reagent with respect to the flowing solutions, to immerse the supported reagent in the solution comprising buffer with no labeled molecules;

g) providing a light source for illuminating an illumination zone within the buffer solution;

h) providing a detector for detecting light emitted from the illumination zone;

i) substantially simultaneously to said switching or directing the flowing solutions with respect to the supported reagent, or switching the location of the supported reagent with respect to the flowing solutions, switching at least one of said light source, detector, or location of said supported reagent to cause the label of a labeled molecule which has reacted with said supported reagent to pass through said illumination zone; and

j) detecting light emitted at said illumination zone to detect the presence of one or more labeled molecules.

2. A method according to claim 1 wherein a single labeled molecule is detected by said step of detecting light emitted at said illumination zone.

3. A method according to claim 1 wherein a chemical reaction is detected by detecting the presence of labeled molecules that have participated in said chemical reaction.

4. A method according to claim 1 wherein a single chemical reaction is detected by detecting the presence of a single labeled molecule that has participated in said chemical reaction by said step of detecting light emitted at said illumination zone.

5. A method according to claim 4 wherein the concentration of said labeled molecules is above 10⁻

8 M.

6. A method according to claim 4 wherein the concentration said labeled molecules is above 10⁻

7 M.

7. A method according to claim 4 wherein the concentration of said labeled molecules is above 10⁻

6 M.

8. A method according to claim 4 wherein the concentration of reactant labeled molecules is above 10⁻

5 M.

9. A method according to claim 1 wherein the label is a fluorescent label.

10. A method according to claim 5 wherein the supported reagent is a complex comprising a surface-bound polymerase enzyme and a nucleic acid or a supported nucleic acid and a polymerase, and the solution of labeled reactive molecules comprises at least one type of fluorescently labeled NTP molecule with no quenching moiety.

11. A method according to claim 10 wherein said fluorescent labels are attached to the beta or gamma phosphate of the NTP.

12. A method according to claim 1 wherein two or more distinguishable types of labels are used to label two or more different types of reactive molecules.

13. A method of claim 1 wherein optical detection of the labels includes identifying the labels by a property selected from the group consisting of color of excitation light or emission light, fluorescence lifetime, fluorescence brightness, electrophoretic mobility, location of detection, or time of detection.

14. A method according to claim 3 wherein an array of supported reagents is used and wherein optical detection of the reactions are separately accomplished for each reagent of the array.

15. A method of claim 3 wherein a series of chemical reactions is detected by repeating said steps of introducing said at least two flowing solutions into said flow cell, immersing said supported reagent in a solution comprising labeled molecules, switching or directing the flowing solutions with respect to the supported reagent, or switching the location of the supported reagent with respect to the flowing solutions, switching at least one of said light source, detector, or location of said supported reagent to cause the label of a labeled molecule which has reacted with said supported reagent to pass through said illumination zone;

and detecting light emitted at said illumination zone to detect the presence of one or more labeled molecules.

16. A method of claim 15 wherein the time interval between successive chemical reactions is controlled by controlling the time between successive repetitions.

17. A system for optically detecting the chemical reaction of a labeled molecule with a surface-bound reagent, wherein the chemical reaction involves at least one step in which the label of the labeled molecule is bound or stereo-chemically entrapped by the reagent, at least for a short interval of time Δ

t exceeding about 100 microseconds, comprising;

a. a surface to which is bound a single reagent molecule, or an array of single reagent molecules at resolvable locations, said surface being contained within a flow cell;

b. an illumination zone;

c. a light source for illuminating said illumination zone;

d. an optical detector for detecting light emitted by a label on said labeled molecule.;

e. at least two flowing solutions, wherein at least one solution comprises labeled molecules that can react with said surface-bound reagent, and at least one solution comprises buffer with no detectable label, and wherein the two solutions exist at distinct locations within said flow cell;

f. a means for switching at least one of the flow of said solutions, the physical location of the surface of said surface-bound reagent, to immerse the surface-bound reagent molecule in only one solution at a time;

g. a means for switching on and off at least one of the light source, the detection of light, or the relative location of the zone of illumination-and-detection and the surface of the surface-bound reagent, so that labels that pass nearby to the surface either pass through said zone or do not pass through said zone; and

h. a circuit for effectively synchronizing said illuminating said illumination zone with said switching at least one of the flow of said solutions or the physical location of the surface of said surface-bound reagent, to immerse the surface-bound reagent molecule in only one solution at a time.