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

摘要

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.

主权项

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 Px, 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 Ax is capable of being produced, wherein each Ax differs by at least two orders of magnitude, andwherein 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 Cx(a) to Cx(b),
wherein Cx(a) is the minimum detectable number of copies of amplicon and Cx(b) is the maximum detectable number of copies of amplicon for probe x,wherein for each probe, Cx+1(a) is greater than Cx(a) and Cx+1(b) is greater than Cx(b) such that the at least two probes together are detectable across a dynamic range of from about 103 to 107, wherein for each amplicon-probe combination, Ax is between Cx(a) and Cx(b), and wherein the at least two probes are capable of producing distinguishable detection signals.