Reaction mixtures for quantitative amplification and detection over a wide dynamic range

Patent metadata

Field	Value
Publication number	US-9347098-B2
Application number	US-201414562922-A
Country	US
Kind code	B2
Filing date	Dec 8, 2014
Priority date	Jul 21, 2009
Publication date	May 24, 2016
Grant date	May 24, 2016

Abstract

Disclosed are compositions and methods for making differentiable amplicon species at unequal ratios using a single amplification system in a single vessel. The number of differentiable amplicons and their ratios to one another are chosen to span the required linear dynamic range for the amplification reaction and to accommodate limitations of the measuring system used to determine the amount of amplicon generated. Unequal amounts of distinguishable amplicon species are generated by providing unequal amounts of one or more amplification reaction components (e.g., distinguishable amplification oligomers, natural and unnatural NTP in an NTP mix, or the like). The amount of target nucleic acid present in a test sample is determined using the linear detection range generated from detection of one or more amplicon species having an amount within the dynamic range of detection.

First claim

What is claimed is:

1. A nucleic acid amplification reaction mixture comprising at least two primers and at least two probes, wherein:
(a) the at least two primers hybridize to the same strand of a target nucleic acid sequence but each primer hybridizes to a distinct nucleotide sequence on the strand,
wherein each primer is present in the reaction mixture at a different amount P x , where x is an integer between 1 and the number of primers in the mixture, and wherein the at least two primers comprise a first inner primer and a second outer primer;

(b) each primer is capable of simultaneously and independently producing one of at least two amplicons from the target nucleic acid sequence under amplification conditions,
wherein for each amplicon, a number of copies A x is capable of being produced, wherein each A x differs by at least two orders of magnitude, and
wherein the at least two amplicons comprise a first amplicon capable of being produced from the first inner primer and a second amplicon capable of being produced from the second outer primer, wherein the first amplicon is shorter than the second amplicon;

(c) the at least two amplicons are detectable by hybridization with the at least two probes, wherein one of the at least two probes is specific to a nucleotide sequence common to both the first and second amplicons and another of the at least two probes is specific to a nucleotide sequence contained within the second amplicon but not within the first amplicon, and each probe is detectable within a detection range C x(a) to C x(b) ,
wherein C x(a) is the minimum detectable number of copies of amplicon and C x(b) is the maximum detectable number of copies of amplicon for probe x,
wherein for each probe, C x+1(a) is greater than C x(a) and C x+1(b) is greater than C x(b) such that the at least two probes together are detectable across a dynamic range of from about 10 3 to 10 7 , wherein for each amplicon-probe combination, A x is between C x(a) and C x(b) , and wherein the at least two probes are capable of producing distinguishable detection signals.

2. The reaction mixture of claim 1 , wherein the reaction mixture further comprises a promoter-primer which operates in a direction opposite the first inner and second outer primers.

3. The reaction mixture of claim 1 , wherein the number of copies of each amplicon A x differs by at least three orders of magnitude.

4. The reaction mixture of claim 1 , wherein the number of copies of each amplicon A x differs by at least four orders of magnitude.

5. The reaction mixture of claim 1 , wherein the amount of each primer differs by at least two orders of magnitude.

6. The reaction mixture of claim 1 , wherein the at least two probes are acridinium ester probes.

7. The reaction mixture of claim 1 , wherein the at least two probes are HICS probes.

8. The reaction mixture of claim 1 , wherein the dynamic range is from about 10 4 to 10 6 .

Assignees

• Gen Probe Inc

Inventors

• Kacian Daniel L
• Browne Kenneth A

Classifications

• C12Q1/6865 Primary

  Promoter-based amplification, e.g. nucleic acid sequence amplification [NASBA], self-sustained sequence replication [3SR] or transcription-based amplification system [TAS] · CPC title

• C12Q1/6813

  Hybridisation assays · CPC title

• C12Q1/6851 Primary

  Quantitative amplification · CPC title

• C12Q2537/143

  Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis · CPC title

• C12Q2545/101

  with an internal standard/control · CPC title