Patent Grant
9249458
This invention relates to the field of nucleic acid chemistry, more specifically to the field of compositions and processes that can serve as primers for the copying of DNA and RNA. Most specifically, this invention relates to compositions of matter that bind to natural DNA and RNA following simple rules as they serve as primers, without binding as strongly to themselves.
Scientists have long sought innovative molecular recognition systems that have binding properties that are useful in different ways. The structures of these systems have been modeled to resemble the structures of DNA and RNA which, in their polymeric form, are called “oligonucleotides”. Further, as with DNA and RNA, the molecular recognition systems have been useful because they bind to other components of the molecular recognition systems and/or to natural DNA and RNA following rules that can be expressed in a form that guides practitioners of ordinary skill in the art and enables them to do useful things.
DNA serves as an archetype to illustrate both molecular structure and rule base recognition. With DNA, three rules (A pairs with T, G pairs with C, the strands are antiparallel) permit the design of two DNA molecules that bind to each other in aqueous solution. When the rules are perfectly followed, two perfectly complementary DNA strands of a substantial length (15-20 nucleotides is normally sufficient in physiological buffers at 37° C.) will bind to each other with substantial selectivity even in complex mixtures containing many other DNA molecules. Heuristic rules have been developed over the years to permit the prediction of general trends in DNA:DNA binding affinity. These have come by performing substantial numbers of melting temperature experiments. For examples as heuristic rules, longer DNA strands generally bind to their partners with higher melting temperatures (Tms) than shorter strands. G:C pairs generally contribute more to duplex stability than A:T pairs. More highly parameterized models improve on the estimates of melting temperatures [All98a] [All98b] [Mar85] [Mat98]. While it remains true that the precise stability of duplexes may not be predictable, that imprecision does not defeat the utility of DNA:DNA binding or require undue experimentation to exploit, even though the number of different DNA sequences of length n (=4n) that would fall within a patent for the DNA molecular recognition system would be enormous.
It has been argued that this rule-based behavior arises because of the repeating charge in the backbone of nucleic acids [Ben04]. Certainly, analogs that have that repeating charges in their backbone maintain their rule-based pairing behavior even if they become quite long. In contrast, the few examples of useful nucleic acid analogs that lack a repeating charge in their backbone do not maintain their rule-based binding behavior in polymers built from two-dozen or more monomer units (fewer if the nucleobases are predominately guanine). The archetypal example of such an uncharged DNA analog is the peptide nucleic acids (PNAs) [Egh92], where rule-based molecular recognition does not survive in longer molecules.
Artificially Expanded Genetic Information Systems (AEGIS)
An archetype of a human-invented rule-based molecular recognition is the artificially expanded genetic information system (AEGIS) disclosed in U.S. Pat. No. 5,432,272. The design of this artificial molecular recognition system began with the observation that two principles of complementarity govern the Watson-Crick pairing of nucleic acids: size complementarity (large purines pair with small pyrimidines) and hydrogen bonding complementarity (hydrogen bond donors from one nucleobase pair with hydrogen bond acceptors from the other). These two principles give rise to the simple rules for base pairing (“A pairs with T, G pairs with C”) that underlie genetics, molecular biology, and biotechnology.
U.S. Pat. No. 5,432,272 pointed out that these principles can be met by nucleotides other than adenine (A) and thymine (T), and guanine (G) and cytosine (C). Rather, twelve nucleobases forming six base pairs joined by mutually exclusive hydrogen bonding patterns might be possible within the geometry of the Watson-Crick base pair.
U.S. Pat. No. 5,432,272 and subsequent patents all taught that the hydrogen bonding pattern that makes an AEGIS component useful as a unit of molecular recognition is distinguishable from the heterocycle that implements it. This means that different heterocycles can often serve interchangeably as molecular recognition elements. This, in turn, permits the elements of an artificial molecular recognition system to be chosen based on considerations other than simple recognition. Thus, the pyADA hydrogen bonding pattern in AEGIS is implemented by thymidine, uridine, uridine derivatives carrying a 5-position linker attached to a fluorescent moiety, uridine derivatives carrying a 5-position linker attached to a biotin, and pseudouridine, for example.
Four features of the AEGIS system make it suited for application:
An archetypal application of AEGIS is in the branched DNA (bDNA) assay used to measure levels of HIV, hepatitis B, and hepatitis C viruses in human patients [Elb04a][Elb04b)]. As this example shows, even though the behavior of DNA duplexes built from AEGIS components having different sequences are not identical and may not be precisely predictable, this has not prevented the AEGIS molecular recognition system from improving the health care of some 400,000 patients annually [Ben04]. This is an illustration of the utility of orthogonality in the analytical chemistry of nucleic acids.
Self Avoiding Molecular Recognition Systems (SAMRS)
A self-avoiding molecular recognition system (SAMRS) has components that bind to natural DNA or RNA, but not to other components of the same unnatural system. In its general description, a SAMRS incorporates nucleobase analogs that replace T, A, G, and C by analogs that are indicated as T*, A*, G*, and C*, which are collectively called “* analogs” of T, A, G, and C respectively. In the simplest implementation of this concept, these * analogs are each able to form two hydrogen bonds to the complementary A, T, C, and G. This means that the T*:A, A*:T, C:*G, and G*:C nucleobase pairs contribute to duplex stability to approximately the same extent as an A:T pair. A SAMRS obtains its self-avoiding properties because the hydrogen bonding groups of the * analogs are chosen the T*:A* and C*:G* nucleobase pairs do not contribute as much to duplex stability because (in the simplest implementation) they are joined by only one hydrogen bond.
As with standard DNA, standard RNA, and oligonucleotides that add non-standard nucleobase pairing, within predicting the binding properties of any sequence within a SAMRS system will be subject to the same imprecision as predicting the properties of an arbitrary DNA or RNA molecule. Thus, as a general rule, if individuals of ordinary skill in the art wish to design a SAMRS sequence that binds to a preselected standard DNA molecule with a Tm of 25° C., they would write down the preselected sequence in the 5′-to-3′ direction, and then write below the SAMRS sequence in an antiparallel direction, matching a T* against every A in the preselected sequence, an A* against every T in the preselected sequence, a C* against every G in the preselected sequence, and a G* against every C in the preselected sequence. It is an open question as to whether such simple instructions allow one of ordinary skill in the art to obtain useful outcomes without undue experimentation. As elaborated below, attempts to obtain such utility failed when we took instruction from the prior art. One object of the instant invention is to provide SAMRS components that provide utility based on precisely this simple a set of rules and instructions.
The need for self-avoiding behaviors has long been pressing when an experimentalist sought to have mixtures containing more than two oligonucleotides, and especially pressing when making libraries of oligonucleotides (defined as having 10 or more oligonucleotide components), especially when those oligonucleotides were to interact with enzymes such as DNA polymerases. This problem is exemplified by multiplexed PCR, where the amplification is sought of many segments of DNA in one pot. This is attempted by adding in large excess two primers flanking each segment, contacting mixture with nucleoside triphosphates, and cycling the mixture up and down in temperature in the presence of a thermostable DNA polymerase. At low temperatures, the primers anneal to the template. At higher temperatures, the polymerase extends the primer to make a product copy of the template. At the highest temperature, the product copy falls off the template, allowing more primers to bind when the temperature is dropped. The primers compete with full length product copies for their binding sites on the template by being present in high concentrations.
While PCR can be successfully multiplexed up to a dozen or so amplicons, with careful design to avoid having the primers present in high concentrations interact with each other, eventually even the most careful design does not prevent primer-primer interactions. These create undesired amplicons, primer dimers, and other artifacts that defeat the utility of the PCR.
This invention combines AEGIS with SAMRS, where a tag containing one or more AEGIS nucleotides is appended to the 5′-end of the molecules that are claimed in the parent application, U.S. patent application Ser. No. 12/229,159, which is incorporated herein in its entirety by reference. This tag has utility, for example, by allowing multiplexed primer extension that is directed by templates built from only natural nucleotides to yield products that have tags that contain one or more AEGIS nucleotides, and therefore do not fully complement any natural oligonucleotide. It also has utility in a process for multiplexed nested PCR of multiple targets [Bro97], where the product amplicons carry one or more tags that contain one or more AEGIS nucleotides, and therefore do not fully complement any natural oligonucleotide.
The goal of the instant invention is to provide primers that could be extended by DNA polymerases when templated on a natural DNA, and to provide primers that could support PCR (which requires that a primer, after being extended, must also be accepted as a template by a DNA polymerase), where the products of these processes have an AEGIS tag.
With both SAMRS and AEGIS, the instant invention teaches a distinction between the hydrogen bonding pattern of a SAMRS system and the heterocycle used to implement it. As is well known in the art, appendages may be attached the 5-position of pyrimidines without interfering with the hydrogen bonding that supports duplex formation. Indeed, 5-position alkyl, allyl, and acetylenic substituents at those positions generally encourage duplex formation. Likewise, substituents at this position may carry tags useful for capture (such as biotin) or detection (such as fluorescent species). The instant invention teaches that similar substituents can be attached at the “5-equivalent” position of the heterocycle that implements the SAMRS and AEGIS, noting that the IUPAC numbering of the heterocycle may assign a different numbering to the 5-equivalent position of any given heterocycle.
Analogous substitutions may be placed at the 7-equivalent position of a 7-deazapurine analog that is a part of a SAMRS and AEGIS. Further, the 7-equivalent nitrogen may be replaced by a CH unit simply to prevent Hoogsteen binding.
Likewise, while 2′-deoxyribose is the preferred backbone when it is desired to have the SAMRS component be recognized by natural DNA polymerases, RNA polymerases, and reverse transcriptases, tighter binding is obtained by placing the SAMRS- and AEGIS-enabling heterocycles on 2′-OMe, 2′-O-alkyl, and/or 2′-O-allyl ribose, PNA, or LNA, which are all taught here as part of the instant invention (such disclosure not being obvious without such a teaching).
The discussion of the inventive steps by which the presently preferred implementations of the SAMRS concept were developed is provided in U.S. patent application Ser. No. 12/229,159, of which this is a continuation-in-part. U.S. patent application Ser. No. 12/229,159 is incorporated in its entirety by reference. The presently preferred implementations of the SAMRS heterocycles are in
As noted in U.S. patent application Ser. No. 12/229,159, reduction to practice discovered as an unexpected phenomenon that the melting temperatures of duplexes supported by only base pairs joined by two hydrogen bonds were abnormally low. Thus, while the 2-thioT:A pair was modestly more stable on average (with the metric being a higher Tm in a variety of contexts) than the T:A pair, a fact well known in the literature, and the I:C pair was significantly less stable than the G:C pair (a fact also well known), duplexes joined by only 2-thioT:A, 2-AP:T, I:C, and 4EtC:G pairs were significantly less stable than expected.
This observation prompted the exploration of primers having the self-avoiding property at the 3′-end of the primer more than at the 5′-end of the primer, as it is overlap of the 3′-ends of primers in primer libraries that causes primer-primer interactions that defeat the PCR analysis. Thus, this would direct one of ordinary skill in the art to place standard nucleobases at the 5′-end.
As a consequence, rules were developed that give the presently preferred embodiments for the primer segments. The preferred 5′-end of the primer is a moiety commonly used in primers, including without limitation OH (the 5′-OH group is free), O-phosphate (allowing the 5′-end to be ligatable), O-oligonucleotide, —NH2, or a phosphate or an amino group linked to a biotin or a fluorescent tag. The 3′-terminal nucleotide preferably has one of the standard nucleotides, adenine (or diaminopurine), thymine, guanine, cytosine, or uracil, or one of the A*, T*, G*, and C* nucleobases, with the most preferred application being a standard nucleotide at the 3′-end. The SAMRS-containing segment next in from the 3′-end is preferably 4 to 6 nucleotides in length, and entirely composed of A*, T*, G*, and C* nucleotides, although a single standard nucleotide can be in segment. The next segments, proceeding away from the 3′-end, are presently preferred to be constructed exclusively from A, T, G, and C, although single SAMRS nucleotides in this region can function as well, preferably if they are thiothymidine or thiouracil. This segment is chosen to give a desired affinity to its complement, and is preferably 10 to 20 nucleotides long. In any case, the presently preferred sum of these two segments primers is at least 15, so as to achieve useful affinity to a target oligonucleotide.
These segments, including the 3′-nucleotide, the SAMRS-rich segment, and the SAMRS-poor segments, are designed to be substantially complementary to a portion of the sequence of a target oligonucleotides, to which it will hybridize in the claimed process.
The preferred AEGIS tag contains nucleobases independently selected from the group consisting of A, T, G, C, K, X, V, J, S, B, Z and P, wherein K, X, V, J, S, B, Z and P are the nucleobases disclosed in
Mosquito-borne arboviruses must be detected in public health surveillance environments. This example combined the self avoiding molecular recognition system (SAMRS), which enables high levels of multiplexing, with an artificially expanded genetic information system (AEGIS), which enables very clean PCR amplification in nested PCR formats. Luminex “liquid microarrays” were exploited for downstream multiplexed detection.
Targets
This example showed this combination supporting single-tube PCR amplification assays to seek RNA from 21 mosquito-borne RNA viruses from the genera Flavivirus, Alphavirus, and Orthobunyavirus. This assay differentiated between many closely-related viral targets, including dengue, West Nile, Japanese encephalitis, and the California serological group viruses.
Flavivirus
Alphavirus
Orthobunyavirus
Primers and Probes
Primers and capture probes containing artificial SAMRS and AEGIS nucleotides (Table 2) were synthesized on ABI 394 and ABI 3900 synthesizers in-house. Primers and capture probes were designed to complement a majority of the strains from each of the target viruses. For the simulants, ssDNA oligonucleotides (Amplimers, Appendix A. Supplementary data Table 2) were chosen arbitrarily to represent a single strain.
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CTAPTCCPCCAPCPAPC
CTAPTCCPCCAPCPAPC
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
CAGPAAGPGGTPGPTPG
CTAPTCCPCCAPCPAPC
CAGPAAGPGGTPGPTPG
PCR and Simulant Preparation
PCR targeting RNA virus simulants was set up in 1× JumpStart reaction buffer (10 mM Tris-HCl, pH 8.3; 50 mM KCl; 1.5 mM MgCl2; 0.001% (w/v) gelatin) (Sigma-Aldrich, St. Louis, Mo.). The other components of the reaction mixture were (in a total volume of 100 μL): 2.5 ng/μL DNA oligo; 0.4 mM dNTPs; 0.4 μM each, Forward T7 primer and Reverse target-specific primer; JumpStart Taq DNA polymerase (2 units, Sigma), nuclease-free ddH2O (added to create a final volume of 100 μL). After the initial denaturation at 95° C. for 2 minutes, 35 cycles of amplification were performed (94° C. for 30 seconds, 55° C. for 30 seconds, and 72° C. for 1 minute). A final extension cycle was run at 72° C. for 5 minutes. Each PCR product (in 100 μL) was ethanol-precipitated and dissolved in nuclease-free dd H2O (12 μL). The resulting PCR products were sequenced in both directions (University of Florida, ICBR) and 5 pmol (about 2 μL) of the concentrated PCR product was used as a T7-DNA template to make RNA simulants.
For simulant production, a T7 RNA polymerase-dependent transcription reaction mixture (20 μL) was set up in a 1× transcription buffer (40 mM Tris, pH7.8, 20 mM NaCl, 18 mM MgCl2, 2 mM spermidine HCl, 10 mM DTT). The reaction mixture contained ATP, CTP, GTP, and UTP (75 mM stock concentration 2 μL each), DNA template (2.5-5 pmol, purified and concentrated PCR product); T7 RNA polymerase (2 μL of a 200 U/μL to give 20 U/μL final concentration). Reaction mixtures were incubated at 37° C. for 8-12 hours. Turbo DNase was then added (2 U per reaction mixture, Life Technologies) to remove DNA template. The mixtures were then incubated at 37° C. for 15-20 minutes. RNA products were isolated by phenol-chloroform extraction and dissolved in nuclease-free water (20 μL). RNA products were resolved by 3% TBE agarose-gel electrophoresis and quantitated by their UV absorbance at 260 nm. The purity of RNAs was evaluated from their A260/A280 ratio. For pure RNA, a ratio of 1.8-2.1 is expected. The absence of template DNA in the RNA samples was confirmed by conventional PCR with Platinum Taq DNA polymerase (Life Technologies) and the ethidium-bromide gel. Samples were aliquoted and kept at −80° C.
Monoplex PCRs were first performed using each target RNA simulant separately to assess the efficacy of the primers in PCR cycling, as well as to determine the sensitivity of the assay. Reactions were then optimized under multiplexed conditions to minimize cross-amplification or cross-hybridization resulting from possible sequence similarity between targets.
Mono- and 21-Fold Multiplexed Nested One-Step RT-PCRs with SAMRS-AEGIS Primers
These were carried out in 1× Reaction mix (Life Technologies) with RNA simulant (4 ng/μL) in a final volume of 20 μL accordingly to the Invitrogen protocol for the SuperScript One-Step RT-PCR with Platinum Taq (Life Technologies). The reaction mixture contained 0.2 mM of dZTP; 0.025 μM each of 21 pairs forward and Reverse hybrid SAMRS-AEGIS target-specific primers; 0.25 μM External AEGIS Forward and Reverse-biotinylated primers; 2.5 units RT/Platinum Taq enzyme Mix. Additional 1.5 mM MgSO4 were added to the RT-PCR buffer. Cycling conditions were: one cycle of the cDNA synthesis and pre-denaturation (53° C. for 30 minutes and 94° C. for 2 minutes), 55 cycles of PCR (94° C. for 15 seconds, 53° C. for 30 seconds, and 70° C. for 30 seconds) and final extension at 72° C. for 5 minute. A “no-target” PCR negative control was included with each assay run. To favor incorporation of biotin-labelled reverse primers to maximize hybridization sensitivity, the second PCR was performed with only reverse biotinylated primer (reverse primer extension reaction, RPER).
Digestion of Excess Primers and dNTPs
To destroy excess primers and deactivate dNTPs prior to RPER, ExoSAP-IT enzyme mixture (2 μL, Affymetrix, Cleveland, Ohio USA) were added to aliquots (5 μL) of standard or SAMRS-AEGIS nested PCR. Reaction mixtures were incubated at 37° C. for 30 minutes and the enzyme mixture was destroyed by heating at 80° C. for 20 minutes. Treated PCR products were added directly to the Reverse Primer Extension reaction.
Reverse Primer Extension Reaction (RPER)
Briefly, a RPER (20 μL) was set up in 1× ThermoPol Buffer (20 mM Tris-HCl, 10 mM (NH4)2SO4, 10 mM KCl, 2 mM MgSO4, 0.1% Triton X-100, pH 8.8 at 25° C.) with 3 μL of each ExoSAP-treated RT-PCR product, 5′-biotinylated external (common) Reverse AEGIS primer (0.2 μM), and Vent (exo-) DNA polymerase (1 unit NEB). Without conversion (an “extension” reaction), dNTPs (final 0.2 mM each) were added. For the dZ incorporation into the final amplicon (“conversion”), nucleoside triphosphates (dATP, dTTP, dGTP, and dZTP, final concentration 0.2 mM of each) were added. The “extension” and “conversion” reaction mixtures were incubated in s BioRad (DNA Engine) Peltier Thermal Cycler at 95° C. for 1 min, followed by 20 cycles (94° C. for 20 seconds, 55° C. for 30 seconds, 72° C. for 30 seconds). A final incubation was run at 72° C. for 1 minute. Reaction mixtures were then held at 4° C. and quenched with 4 mM EDTA.
For standard RT-PCR products, a set of 21 reverse target-specific primers (0.2 μM each) was added to the “extension” or “conversion” reactions. The other reaction components were the same as above.
Probe Coupling to Beads
Capture probes modified with an amino-C12 linker at the 5′-end were coupled to Luminex MicroPlex carboxylated micro-spheres (“beads”) by a carbodiimide-based procedure according to the manufacturer's protocol. Briefly, for each combination of probe and bead set (Table 5), 2.5 million Luminex beads were resuspended in 0.1 M MES buffer (morpholine ethane sulfonic acid, 50 μL, pH 4.5) with probe (4 μL of 0.1 mM stock to give 0.4 nanomole final concentration), and treated twice with 1-ethyl-3-[3-dimethylamino-propyl]-carbodiimide hydrochloride (EDC, 5 μL of a 10 mg/mL solution, Thermo Scientific/Pierce, Rockford, Ill.) at room temperature for 30 min, rinsed in Tween 20 (0.02% aqueous solution), then rinsed with a sodium dodecylsulfate solution (0.1%), and resuspended in Tris-EDTA buffer (pH 8.0) to 5.0.
Luminex Direct Hybridization (DHA)
This was performed accordingly to the “no wash” Luminex protocol (http://www.luminexcorp.com/Support/SupportResources/). In a pilot experiment “wash” and “no wash” Luminex protocols were compared; no differences were found between two protocols when applied to our target-specific probes' design. Briefly, aliquots (5 μL) of each extension or conversion reaction were transferred to 96-well plates (96-well PCR thermo polystyrene plates; Costar). Hybridization buffer (25 μL of 2×Tm 0.4 M NaCl; 0.2 M Tris, 0.16 Triton X-100, pH 8.0) containing 100 of each target-specific probe-coupled microsphere set per μL or totally 2,500 target-specific probe-coupled each microsphere types. Microspheres were vortexed and sonicated for 20 seconds. The total volume was adjusted to 50 μL by 20 μl of ddH20. 25 μl of ddH20 were added to each Background well (negative control). Hybridization was performed at 55° C. accordingly to the direct hybridization protocol (DHA) provided by Luminex: 95° C. for 5 min, cool to 55° C. at a speed of 0.1° C./second, 15 mM at the hybridization T 55° C. Tm buffer (25 μL of 1×) containing streptavidin-R-phycoerythrin (2 μg, PJRS14, PROzyme) were added to the each hybridization mixture, which was then incubated at 56° C. for 5 min. Hybridization reactions were carried out in triplicate, and “no-target” controls were run in replicates of 6. Beads were analyzed for internal bead color and R-phycoerythrin reporter fluorescence using a Luminex 200 analyzer (Luminex xMAP Technology, Luminex Corporation) and the xPonent Software solutions. The median reporter fluorescence intensity (MFI) was computed for each bead type in the sample. The instrument's gate setting was established before the samples were run, and was maintained throughout the course of the study.
Results
Twenty-one mosquito-borne arboviruses were selected (Table 1) to assemble and develop xMAP Luminex assays diagnostic panel based on PCR amplification and using the artificial SAMRS-AEGIS technology [Yan10; Yan13].
Viral simulant RNAs were produced in vitro by transcription of the appropriate templates using T7 RNA polymerase. In pilot experiments, SuperScript One-Step RT-PCR with Platinum Taq (Life Technology) was found to be more sensitive and robust than other enzyme combinations tested, and thus able to support the nested PCR amplification with external primers containing the nonstandard P nucleotide, which pairs with the Z nucleotide. The target-specific standard or hybrid SAMRS-AEGIS forward and reverse primer pairs designed for the panel were tested first by monoplexed one-step RT-PCR with viral RNA simulants. Each monoplexed RT-PCR produced the expected amplicons, which were visualized by the ethidium-bromide staining following electrophoresis. Multiplexed RT-PCR conditions were established in a series of preliminary experiments (data not shown). Finally, multiplexed nested RT-PCRs were executed with each viral target using 21 pairs of specific SAMRS-AEGIS primers and AEGIS external primers (Table 2). PCR amplicons generated under optimized conditions were visualized on ethidium bromide gel as clearly resolved bands of the expected sizes ranging from 59 to 160 base pairs. The PCR negative control showed non-substantial level of primer-dimerization.
Amplicons containing only standard nucleotides were also produced by multiplexed one-step RT-PCRs and analyzed by agarose-gel electrophoresis. The 21-fold multiplexed reactions were primed with full set of target-specific primers, each at the final concentration of 0.4 The standard PCR amplicons were visualized on the ethidium bromide gel as clearly resolved bands of the expected sizes.
Continuation in part of U.S. patent application Ser. No. 12/229,159 filed 2008 Aug. 20 Which is a Continuation in part of U.S. patent application Ser. No. 11/647,609 filed 2008 Dec. 30 Which is a Continuation in part of U.S. patent application Ser. No. 11/271,366 filed 2005 Nov. 12 Which is based on provisional patent applications 60/627,460 and 60/627,459 filed 2004 Nov. 13 and 60/654,424 filed 2005 Dec. 20
This invention was made with government support under W911NF12C0059 awarded by The Office of the Secretary of Defense US Army RDECOM ACQ CTR. The government may have certain rights in the invention.
| Number | Name | Date | Kind |
|---|---|---|---|
| 5432272 | Benner | Jul 1995 | A |
| 8871469 | Benner et al. | Oct 2014 | B1 |
| Number | Date | Country | |
|---|---|---|---|
| 60627460 | Nov 2004 | US | |
| 60627459 | Nov 2004 | US | |
| 60654424 | Feb 2005 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12229159 | Aug 2008 | US |
| Child | 14524227 | US | |
| Parent | 11647609 | Dec 2006 | US |
| Child | 12229159 | US | |
| Parent | 11271366 | Nov 2005 | US |
| Child | 11647609 | US |
