Systems and methods for multiplex analysis of PCR in real time

• US 9,193,991 B2
• Filed: 09/29/2014
• Issued: 11/24/2015
• Est. Priority Date: 12/13/2006
• Status: Active Grant

• Current Assignee: Luminex Corporation (DiaSorin S.p.A.)
• Original Assignee: Luminex Corporation (DiaSorin S.p.A.)
• Inventors: Whitman, Douglas F., Collins, Charles J.
• Primary Examiner(s): Horlick, Kenneth R.
• Assistant Examiner(s): THOMAS, DAVID C
• Application Number:
  US14/499,304
• Publication Number:
  US 20150017646A1
• Time in Patent Office: 421 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: C12Q 1/6804 Nucleic acid analysis using immunogens immunoassay G01N33/53
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 1/6834 Enzymatic or biochemical coupling of nucleic acids to a solid phase
• CPC Class Codes: C12Q 1/6837 using probe arrays or probe chips C12Q1/6874 takes precedence
• CPC Class Codes: C12Q 1/686 Polymerase chain reaction [PCR]
• CPC Class Codes: C12Q 2531/113 PCR
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2561/113 Real time assay
• CPC Class Codes: C12Q 2563/143 Magnetism, e.g. magnetic label

Abstract

The present invention provides methods and systems for real-time measurements of PCR with multiplexing capability. Certain embodiments relate to methods and systems that use fluorescently encoded superparamagnetic microspheres for the immobilization of amplification products during the PCR process, and an imaging chamber of a measurement device that is also capable of controllable thermal cycling for assisting the PCR process.

Claims

1. A method for multiplexed detection of nucleic acid targets in a sample comprising:

(a) combining in a chamber a sample, a plurality of primer pairs for priming amplification of nucleic acid targets in the sample, a plurality of first probes immobilized on a plurality of encoded particles such that the identity of each first probe is known from the encoded particle on which it is immobilized, and a plurality of second probes complementary to the nucleic acid targets and to the plurality of first probes, wherein the second probes (i) are labeled, and (ii) are not immobilized on the plurality of encoded particles;

(b) forming amplification products in the chamber for each of the nucleic acid targets amplified with the plurality of primer pairs;

(c) measuring a signal over time from the encoded particles and a signal over time from the label of the second probes hybridized to the first probes immobilized on the encoded particles, wherein the encoded particles are immobilized on a surface of the chamber, and wherein a change in the signal from the label of the second probes hybridized to the first probes immobilized on the encoded particles indicates the presence of the target nucleic acids; and

(d) detecting the presence or absence of the nucleic acid targets in the sample based on the change in the signal from the label of the second probes hybridized to the first probes immobilized on the encoded particles.

2. The method of claim 1, wherein the sample comprises between 8 to 60 distinct nucleic acid targets.

3. The method of claim 1, wherein the second probes are labeled with a fluorescent dye.

4. The method of claim 1, wherein the second probes are labeled with a quencher and the first probes are labeled with a fluorescent dye.

5. The method of claim 1, wherein the second probes are labeled with one member of a fluorescence resonance energy transfer pair and the first probes are labeled with the other member of the fluorescence resonance energy transfer pair.

6. The method of claim 1, wherein the encoded particles are encoded microspheres.

7. The method of claim 6, wherein the encoded microspheres are encoded with fluorescent dyes.

8. The method of claim 6, wherein the encoded microspheres comprise polystyrene.

9. The method of claim 1, wherein the encoded microspheres are magnetic microspheres and the magnetic microspheres are immobilized on the surface of the chamber by a magnetic field.

10. The method of claim 1, wherein the first probes are attached to the encoded particles at their 5′

ends.

11. The method of claim 1, wherein melting temperature between the second probes and the first probes is lower than the binding temperature between the first probes and the nucleic acid targets.

12. A method for multiplexed detection of nucleic acid targets in a sample comprising:

(a) combining in a chamber a sample, a plurality of labelled probes complementary to a plurality of nucleic acid targets that may be present in the sample, and a plurality of primers complementary to the plurality of nucleic acid targets such that extending the primers on the nucleic acid targets using a polymerase with exonuclease activity results in hydrolysis of the labelled probes hybridized to the same nucleic acid target, wherein the labelled probes are immobilized on a plurality of encoded particles such that the identity of each probe is known from the encoded particle on which it is immobilized;

(b) performing a plurality of amplification cycles using a polymerase with exonuclease activity such that extending the primers on the nucleic acid targets using the polymerase with exonuclease activity results in hydrolysis of the labelled probes hybridized to the same nucleic acid target;

(c) measuring a signal over time from the encoded particles and a signal over time from the labeled probes immobilized on the encoded particles, wherein the encoded particles are immobilized on a surface of the chamber, and wherein a change in the signal from the labeled probes indicates hydrolysis activity, which indicates the presence of the target nucleic acid; and

(d) detecting the presence or absence of the nucleic acid targets in the sample based on the change of the signal from the labeled probes immobilized on the encoded particles.

13. The method of claim 12, wherein the encoded particles are encoded micro spheres.

14. The method of claim 13, wherein the encoded microspheres are encoded with fluorescent dyes.

15. The method of claim 13, wherein the encoded microspheres are magnetic microspheres.

16. The method of claim 15, wherein the magnetic microspheres further comprise a fluorophore affixed to the surface of the magnetic microspheres.

17. The method of claim 12, wherein the labelled probes are labelled with a fluorophore and quencher pair or with a FRET pair.

18. The method of claim 12, wherein the labelled probes are labelled with a fluorophore.