Patent Application
20150037797
This application contains references to amino acid sequences and/or nucleic acid sequences which have been submitted concurrently herewith as the sequence listing text file “2228736.1.txt”, file size 3.15 KiloBytes (KB), created on August 2014. The aforementioned sequence listing is hereby incorporated by reference in its entirety pursuant to 37 C.F.R. §1.52(e)(5).
The present invention relates to methods and kits for detecting a nucleic acid in a biological sample.
Very recently, molecular diagnostics has increasingly gained in importance. It has found an entry into the clinical diagnosis of diseases (inter alia detection of infectious pathogens, detection of mutations of the genome, detection of diseased cells and identification of risk factors for predisposition to a disease). However, in the meantime molecular diagnostic methods are also finding their uses in veterinary medicine, environmental analysis and foodstuff testing.
In particular, through the determination of gene expression in tissues, nucleic acid analysis opens up very promising new possibilities in the study and diagnosis of disease.
In order to reduce costs and keep the processing time from sample receipt to determination of the analytical result (also referred to as “time to result”) as short as possible, it is a priority target to make methods for detecting nucleic acids as efficient as possible and as far as possible to perform them with automation. This applies particularly to diagnostics. Those methods which can be carried out in reaction vessels differing as little as possible and can be carried out in standardized formats (e.g. 96-well microtiter plate format) are well suited for automation since in these methods efficient pipetting robots can be used. Hence in the state of the art there is the need for simple, efficient and automatable sample analysis.
Today, specific nucleic acid sequences are typically detected or quantified by e.g. heterogenous hybridization assays, PCR methods, or direct sequencing. Those types of assays typically have a quite long time to result, which makes them difficult to apply for critical medical situations e.g. in the course of cardiac events. Moreover, the current tests are not adaptable to immunoassay analyzers, which are the most prominent platforms in the clinical laboratory or in point-of-care settings such as emergency rooms.
Nucleic acids of interest to be detected include genomic DNA, expressed mRNA and other RNAs such as MicroRNAs (abbreviated miRNAs). MiRNAs are a new class of small RNAs with various biological functions (A. Keller et al, Nat Methods. 2011 8(10):841-3). They are short (average of 20-24 nucleotide) ribonucleic acid (RNA) molecules found in eukaryotic cells. Several hundred different species of microRNAs (i.e. several hundred different sequences) have been identified in mammals. They are important for post-transcriptional gene-regulation and bind to complementary sequences on target messenger RNA transcripts (mRNAs), which can lead to translational repression or target degradation and gene silencing. As such they can also be used as biologic markers for research, diagnosis and therapy purposes. In the prior art miRNAs are also detected and quantified by heterogenous hybridization assays or direct sequencing. It is a particular challenge to reliably quantify miRNAs as these are inherently chemically unstable and prone to degradation. This is due to the chemical instability of RNA, the fact that miRNA are present as single strand nucleic acids and due to their short length.
In a different approach, Quavit et al (Anal. Chem., 2011, 83(15), pp 5949-5956) employ oligo-nucleotide-coated gravimetric sensors to bind miRNAs. The resultant hybrids are bound by anti DNA:RNA antibodies and the mass difference between hybrid and hybrid with bound antibody is gravimetrically detected. As the nucleic acid probes are part of the sensor, this approach is inflexible with regard to target nucleic acid of interests, as an individual sensor needs to be configured for each target nucleic acid of interest.
A further problem is that many applications in molecular-biological research and diagnostics require determining the amount or concentration of particular nucleic acids in a sample. The standard method for quantifying nucleic acids is by PCR reaction, employing an internal standard of known concentration and/or using real-time PCR. Disadvantageously, however, these methods have a limited dynamic range. The typical dynamic range is between 1 to 100 and 1 to 1000, but the range of nucleic acid concentrations to be measured often is distinctly larger, for example 1 to 1 000 000. Further, PCR methods have been perceived as unreliable for quantization due to the possibility of contamination and nonlinear enzyme kinetics.
The technical problem underlying the present invention is to provide a method for the detection of nucleic acid molecules which is easily adaptable to nucleic acid molecules with different sequences and which is easily adaptable to automated laboratory platforms or point-of care type settings.
It is a further object of the invention to provide a method for the detection of nucleic acid molecules which allows to obtain quantifiable results with an improved dynamic range.
It is another object of the present invention to provide a method suitable for the detection and/or quantification of miRNAs.
It is another object of the present invention to provide a kit for the detection of nucleic acid molecules meeting the above criteria.
Before the invention is described in detail, it is to be understood that this invention is not limited to the particular component parts of the process steps of the methods described as such methods may vary. It is also to be understood that the terminology used herein is for purposes of describing particular embodiments only, and is not intended to be limiting. It must be noted that, as used in the specification and the appended claims, the singular forms “a,” “an” and “the” include singular and/or plural referents unless the context clearly dictates otherwise. It is also to be understood that plural forms include singular and/or plural referents unless the context clearly dictates otherwise. It is moreover to be understood that, in case parameter ranges are given which are delimited by numeric values, the ranges are deemed to include these limitation values.
An embodiment of the invention relates to a method of detecting nucleic acid molecules by immunoassay detection. Detection of a specific nucleic acid molecule of interest is achieved by using a nucleic acid probe in solution which hybridizes in solution to the nucleic acid molecule of interest. Immunoassay detection is achieved by using an antibody specific for the hybrid formed by hybridization of the nucleic acid probe to the nucleic acid molecule of interest.
In the most general terms, the invention relates to a method of detecting nucleic acid molecules by immunoassay detection. Detection of a specific nucleic acid molecule of interest is achieved by using a dissolved nucleic acid probe which hybridizes to the nucleic acid molecule of interest. Immunoassay detection is achieved by an antibody specific for the hybrid formed by hybridization of the nucleic acid probe to the nucleic acid molecule of interest. The antibody can be provided in a form which is bound to a solid phase. Alternatively the antibody can be provided in solution and the nucleic acid of interest can be detected in a homogeneous immunoassay. The hybrid is provided in solution. This solution is brought into contact with the antibody. The antibody will bind the hybrid and the complex of antibody and bound hybrid can be detected. This allows easy adaptation to nucleic acid molecules with different sequences and easy adaptation to automated laboratory platforms or point-of care type settings and devices. Such an antibody can e.g. be obtained by immunizing a host organism with the respective hybrid (e.g. a RNA:DNA hybrid) and collecting antibodies or antibody-producing cells, as is known in the art.
The method and kit of the invention allow a fast and homogenous detection and quantification of specific nucleic acid sequences such as miRNAs.
As immunoassays typically have short times to result, and are adaptable to immunoassay analyzers, this novel assay format overcomes the problems of the current test formats mentioned above.
Unless defined otherwise, technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
The term “antibody”, as used herein, refers to an immunoglobulin protein or a fragment thereof, said fragment being capable of specifically binding an antigen. An antibody, including an antibody fragment, suitable for the invention may be monoclonal, polyclonal, of any host organism source, recombinantly expressed or otherwise artificially produced and of any immunoglobuline type. In the context of the invention, the antibody is able to bind an antigen comprising a hybrid of a nucleic acid molecule of interest and a nucleic acid probe.
The term “hybridization”, as used herein, refers to the process of combining complementary, single-stranded nucleic acids or nucleotide analogues into a single double stranded molecule, the so-called “hybrid”. Nucleotides or nucleotide analogues will bind to their complement under normal conditions, so two complementary strands will bind to each other readily. Single stranded probes can be used in order to find complementary target sequences. If such sequences exist in the sample, the probes will hybridize to said sequences which can then be detected.
The term “immunoassay”, as used herein, refers to the detection or quantification of an analyte—such as a nucleic acid of interest—comprising an immune reaction between an antibody and an antigen. In the context of the invention the analyte to be detected or quantified comprises a nucleic acid of interest.
A “label moiety” within the meaning of the invention, shall have the ordinary meaning of this term which is well known to the person skilled in the art of molecular biology. The label moiety may comprise a binding partner of a specific binding pair, wherein the respective binding reaction is used to couple the label moiety to a detectable label. Further, the label moiety itself may comprise any detectable label. Detection may be achieved in any suitable fashion, e.g. by optical detection, chemical detection, electrochemical detection, radioactive detection, magnetic detection or any other suitable mode of detection. Examples for label moieties include enzymatic labels, chromogenic labels, fluorescent labels, chemiluminescent labels, radioactive labels, and magnetic labels.
The term “marker” or “biomarker” refers to a biological molecule, e.g., a nucleic acid, peptide, protein, hormone, etc., whose presence or concentration can be detected and correlated with a known condition, such as a disease state.
The term “nucleic acid” is intended to indicate any nucleic acid molecule and/or analogous molecules comprised of a sequence of nucleotides including DNA, cDNA and/or genomic DNA, RNA, preferably miRNA, peptide nucleic acid (PNA), locked nucleic acid (LNA) and/or morpholino.
“Nucleic acid of interest”, within the meaning of the invention refers to a target nucleic acid which is to be detected and/or quantified. In particular, this term refers to a nucleic acid having a specific predetermined sequence.
“Nucleic acid probes”, within the meaning of the invention, shall have the ordinary meaning of this term which is well known to the person skilled in the art of molecular biology. In a preferred embodiment of the invention they shall be understood as being polynucleotide molecules having a sequence identical, complementary, or homologous to the complement of regions of a target nucleic acid of interest which is to be detected or quantified. In yet another embodiment, nucleotide analogues are also comprised for usage as nucleic acid probes.
The terms “sample”, “biological sample”, or “clinical sample”, as used herein, refer to any sample containing a nucleic acid of interest. A sample may be obtained from a patient. The sample may be of any biological tissue or fluid. Such samples include, but are not limited to, sputum, blood, serum, plasma, blood cells (e.g., white cells), tissue, biopsy samples, smear samples, lavage samples, swab samples, cell-containing body fluids, free floating nucleic acids, urine, peritoneal fluid, and pleural fluid, liquor cerebro-spinalis, urine, feces, tear fluid, or cells therefrom. Biological samples may also include sections of tissues such as frozen or fixed sections taken for histological purposes or microdissected cells or extracellular parts thereof.
The term “solid phase”, as used herein, refers to an object which consists of a porous and/or nonporous, material which is insoluble in the solvent system used (e.g. water insoluble). It can have a wide variety of forms such as vessels, tubes, plates, spheres, microparticles, rods, strips, filter paper, chromatography paper, etc. The term “solid phase bound” refers to an object, such as an antibody, being attached to the solid phase in such a way that it will not become detached and dissolved into solution when the methods of the invention described herein are performed. Binding may be achieved for example by physissorbtion, chemisorption, covalent linking, as is known in the art.
To meet the need for a flexible assay system for the detection and/or quantification of miRNAs in e.g. a clinical laboratory setting, the present invention provides a method for the immunoassay detection of specific nucleic acid sequences such as miRNAs. This provides an alternative to existing methods. Immunoassays typically have short times to result, and are adaptable to automated immunoassay analyzers.
In a further aspect, an embodiment of the invention relates to a method for detecting a nucleic acid molecule of interest in a sample, comprising the following steps:
providing a nucleic acid probe in solution;
hybridizing the nucleic acid molecule of interest to the nucleic acid probe to obtain hybrids of said nucleic acid molecule of interest and said nucleic acid probe;
binding said hybrid to an antibody capable of specifically binding nucleic acid hybrids, wherein the antibody is bound to a solid phase; and
detecting the antibody-bound hybrid.
According to this aspect, binding of the antibody to the hybrid is achieved by bringing the solid-phase bound antibody into contact with the solution containing the hybrid. Because one of the binding partners forming the detectable complex of antibody and hybrid is solid-phase bound, this aspect of the invention can be referred top as a “hetereogeneous” format. A particular advantage of this format lies in the ability to provide a solid phase with a bound antibody, wherein the antibody serves as a universal capture moiety for the hybrids. This allows for convenient assay formats, where the antibody is pre-coated onto commonly used sold phase formats such as microtiter plates, test strips, articles and the like.
In a further aspect, an embodiment of the invention relates to a method for detecting a nucleic acid molecule of interest in a sample, comprising the following steps:
providing a nucleic acid probe in solution;
hybridizing the nucleic acid molecule of interest to the nucleic acid probe to obtain hybrids of said nucleic acid molecule of interest and said nucleic acid probe;
binding said hybrid to an antibody capable of specifically binding nucleic acid hybrids, wherein the antibody is in solution; and
detecting the antibody-bound hybrid in solution.
According to this alternative aspect, binding of the antibody to the hybrid is achieved by bringing the antibody in solution into contact with the solution containing the hybrid. Because of both binding partners forming the detectable complex of antibody and hybrid being in solution, this aspect of the invention can be referred to as a “homogeneous” format.
In both the homogeneous and the heterogeneous format, the nucleic acid probe is provided in solution and hybridization takes place in solution. This makes both formats easily adaptable to the detection of different nucleic acids of interest (by selecting the nucleic acid probe accordingly), and it also makes both formats easily adaptable to automated analysis systems such as are commonly used in clinical laboratories.
In a further aspect, an embodiment of the invention relates to a method wherein the antibody is bound to a competitive antigen prior to the binding of said first hybrid and said hybrid is detected by displacement of the competitive antigen.
The competitive antigen can be a competitive hybrid of nucleic acids. Further, the competitive hybrid can carry a label moiety. Well known detection technologies for competitive immunoassays, such as FRET (fluorescence resonance energy transfer) or EMIT (Enzyme multiplied immunoassay technique), can be employed.
Advantageously, the methods of the invention allow the detection of many different species (i.e. having different sequences) of nucleic acid of interest with the same antibody serving as a universal capture moiety. Specific detection of an individual species is achieved by using a nucleic acid probe which will hybridize to the individual species of the nucleic acid of interest. Further, advantageously, these methods offer a high dynamic range. Immunoassays routinely offer a dynamic range from 1:1000 to 1:100000 which can easily be increased further by performing a simple dilution series.
According to a further aspect of the invention, the nucleic acid molecule of interest is an RNA. In this case it is also contemplated that the RNA can be converted to complementary DNA (cDNA) prior to performing the method of the invention.
According to a further aspect of the invention, the nucleic acid probe is a DNA.
According to a further aspect of the invention, the antibody is specific for DNA/RNA hybrids.
According to a further aspect of the invention, the nucleic acid probe is labelled with a label moiety. According to a preferred embodiment the label moiety is provided by biotinylation of the nucleic acid probe. This allows detection by using a detectable label coupled to streptavidin.
According to a further aspect of the invention, the labeling moiety comprises an enzyme. A plurality of enzyme-substrate detection chemistries are commercially available. They are well established both for e.g. microtiter-plate formats micro-particle formats and test strip formats and are compatible with commercially available analyzer systems and testing devices and their detectors. According to a preferred embodiment the label moiety is provided by biotinylation of the nucleic acid probe and use of a strepatavidin-enzyme conjugate as detectable label. The use of an enzymatic label offers a further path to increasing dynamic range. As a detecable product is developed in an accumulating enzymatically catalyzed reaction between enzyme and substrate(s), the sample can be read when the reaction has developed to a degree where signal is well over background and within the linear range of the detection system. Many enzyme-substrate chemistries further offer the possibility to use stop solutions which usually comprises the addition of a substance that will stop enzymatic activity. In this way, the enzymatically catalyzed reaction can be stopped once it has progressed to an appropriate degree and the sample can be read either immediately or at a later point in time without the danger of “overdeveloping.”
According to a further aspect of the invention, the nucleic acid molecule of interest is a miRNA. As several hundred mi-RNA species are known in humans, the method and kit of the invention are particularly well suited for the detection and quantification of miRNAs. Simply by providing the appropriate nucleic acid probe it is possible to adapt the method and kit of the invention for the detection of any number of miRNAs.
According to a further aspect of the invention, the detection is a quantitative detection. If desired, the concentration can be measured as an absolute concentration, for example, by using an internal standard (a known nucleic acid with a known initial concentration, which is added to the sample or is amplified and measured in parallel). In many cases it may be sufficient to determine the relative concentration of the nucleic acid of interest in the test sample against a reference sample, e.g. by comparing a patient sample against a sample from a healthy control.
According to a further aspect of the invention, a plurality of different nucleic acids of interest are detected by using a respective plurality of nucleic acid probes.
An embodiment of the invention further relates to a kit for detecting a nucleic acid molecule of interest in a sample, said kit being useful for carrying out the methods of the invention, comprising at least a nucleic acid probe in solution or in a dissolvable form and an antibody capable of binding a hybrid of said nucleic acid molecule of interest to said nucleic acid probe.
In the kit of the invention, the nucleic acid probe can be provided in a solution, either as a working solution or as a dilutable stock solution. Alternatively it can be provided in a dissolvable form, for example in lyophilized form.
The kit may further comprise any or all of the following: controls, standards, calibrators developing solutions for developing detectable labelling reactions, stop solutions for stopping development of a labelling reactions, blocking solutions for blocking unspecific binding or hybridization, wash solutions for reduction of unspecific background signal etc., as is known in the art.
According to a further aspect of the invention, the kit further comprises the antibody bound to a solid phase. A particular advantage of this type of kit lies in the ability to provide a solid phase with a bound antibody, wherein the antibody serves as a universal capture moiety for the hybrids. This allows for convenient assay formats, where the antibody is pre-coated onto commonly used sold phase formats such as microtiter plates, test strips, articles and the like.
According to a further aspect of the invention, the kit further comprises a support for supporting the solid phase to which the antibody is bound.
According to a further aspect of the invention, the solid phase can have a very wide variety of forms, for example those of vessels, tubes, microtitration plates, spheres, microparticles, rods, strips, filter paper, chromatography paper, etc. As a rule, the surface of the solid phase is hydrophilic or can be made hydrophilic. The solid phase can consist of a very wide variety of materials, for example of inorganic and/or organic materials, of synthetic materials, of naturally occurring materials and/or of modified naturally occurring materials. Examples of solid phase materials are polymers, such as cellulose, nitrocellulose, cellulose acetate, polyvinyl chloride, polyacrylamide, crosslinked dextran molecules, agarose, polystyrene, polyethylene, polypropylene, polymethacrylate or nylon; ceramic, glass or metals, in particular precious metals such as gold and silver; magnetite; mixtures or combinations thereof; etc. Cells, liposomes and phospholipid vesicles are also covered by the term solid phase.
The solid phase can also possess a coating consisting of one or more layers, for example of proteins, carbohydrates, lipophilic substances, biopolymers or organic polymers, or mixtures thereof, in order, for example, to suppress or prevent the nonspecific binding of sample constituents to the solid phase or in order, for example, to achieve improvements with regard to the suspension stability of particular solid phases, with regard to storage stability, with regard to dimensional stability or with regard to resistance to UV light, microbes or other agents having a destructive effect.
According to a further aspect of the invention, the support comprises a microtiter plate.
According to a further aspect of the invention, the support comprises a test strip. The test strip can be of a simple dip format, wherein the strip is dipped into a sample fluid. It can also be embedded in a cassette, wherein a drop of sample fluid is transferred into an appropriate opening of the cassette.
It is to be understood that the support itself or a portion thereof may serve as solid-phase to which the antibody is bound. In the case of the support being a microtiter plate with at least one or a plurality of wells, the antibody can be coated on the interior surface (or on a portion thereof) of the well(s). In the case of the support being a test strip, the antibody can be coated on a portion of the test strip, e.g. on one or several distinct bands on the strip thus yielding a corresponding pattern of labelled bands when the test is performed.
The support may have distinct portions dedicated to controls, as is known in the art.
According to a preferred embodiment of the invention the method and kit can be in an ELISA format (Enzyme-linked immunosorbent assay). This format essentially combines the use of a solid-phase bound antibody with the use of an enzymatic label, i.e. a label moiety comprising an enzyme. Preferably, in a further variation of this preferred embodiment, suitable microtiter plates are coated with the antibody which will bind the hybrid. In a different variation of this preferred embodiment, a test strip or similar simple solid-phase device is pre-coated with the antibody which will bind the hybrid. In this form, the invention is well suited for use in a point-of care setting, e.g. in the emergency room.
According to a preferred embodiment of the invention, the nucleic acid probe may be labelled. In this way the hybrid will be easily detectable allowing for a simple, straightforward assay format. Alternatively, the complex of antibody and hybrid may be detected by a further suitable secondary antibody in a type of Sandwich-immunoassay format.
According to a preferred embodiment of the invention the kit may comprise the antibody in a solid phase-bound form on pre-coated microtiter plates, coated beads, test strips and the like. In this way multiplex assay are easily possible, where a combination of the solid phase-bound antibody with a plurality of nucleic acid probes can be used to detect a corresponding plurality of nucleic acids of interest. For example, in a microtiter plate, such as a 96-well plate, can be pre-coated with the antibody and different nucleic acid probes can be used in different wells to detect different nucleic acids of interest. Alternatively, different nucleic acid probes with different label moieties may be used in the same assay to detect different nucleic acids of interest.
By using an antibody bound to a solid phase as a universal capture moiety for hybrids comprising different combinations of nucleic acids of interest and respective nucleic acid probes a plurality of assays can be performed in parallel, e.g. using the same solid phase, such as an antibody-coated microtiter plate. Hybridization can be e.g. performed in a PCR machine or similar heating device which allows to select a predetermined temperature for hybridization. If such a heating device allows the application of a temperature gradient across the field of the microtiter plate, an optimal hybridization temperature can be quickly determined. Moreover, by using an antibody bound to a solid phase as a universal capture moiety it then becomes possible to perform hybridizations with a plurality of nucleic acid probes at a corresponding plurality of differing optimal hybridization temperatures. This can be done e.g. in separate wells of the same microtiter plate.
The method of the invention, wherein the antibody as a universal capture moiety for hybrids is provided in a solid phase-bound form and the hybrid (comprising the nucleic acid probe) as capture target is added in solution thus offers many advantages in terms of both adapting the method to multiplex assays and adapting the method to existing analyzer systems, devices, and workflows.
According to a preferred embodiment of the invention, the antibody is bound to a solid phase and the nucleic acid probe is labelled with a labelling moiety. This embodiment provides for a straightforward assay protocol and short time to result.
The method and kit of the invention provide a simple, specific, and sensitive way to detect a nucleic acid of interest which is easily adaptable to existing automated analyzer systems such as are used in central laboratory of hospitals or doctor's offices.
The method and kit of the invention have proven to be particularly useful for the detection of miRNAs. They allow a fast and accurate detection which can be carried out on automated analyzer systems.
Additional details, features, characteristics and advantages of the object of the invention are further disclosed in the following description of the respective examples, which, in an exemplary fashion, show preferred embodiments of the invention. However, these examples should by no means be understood as to limit the scope of the invention.
Briefly, in a first step, a defined quantity of biotin labelled sequence-specific DNA oligonucleotide is hybridized to the miRNA from e.g. a patient sample under conditions that only a single miRNA species can hybridize. The amount of RNA:DNA hybrids generated during this step is proportional to the amount of the specific miRNA species present in that sample. In a second step, the hybridisation mixture is transferred to a solid phase coated with a mAb to RNA:DNA hybrids; any hybrids present will bind to the solid phase. Binding of RNA:DNA hybrids is detected by a suitable label system e.g. Streptavidin-peroxidase (Streptavidin-POD). The amount of POD bound is proportional to the amount of RNA:DNA hybrids present in the original sample.
Detection and quantification of miRNA is inherently difficult. Surprisingly and unexpectedly, it has been found that this method allows for a highly specific, sensitive and reproducible detection of miRNAs. Without wishing to be bound to this theory, the inventors suspect that this may be due to stabilization of miRNAs in a double-stranded hybrid in solution, in particular in RNA:DNA heteroduplexes. It can be shown that the hybrids in solution can be frozen, stored for long periods of time and subsequently still be detected with high sensitivity in the method of the invention.
In an experiment the miRNAs miR-7, miR-380 or miR-1254 were hybridized to complementary DNA oligonucleotides, or to a non-specific DNA oligonucleotide as control. After hybridization, the DNA:RNA hybrid solutions were transferred to the wells of an ELISA plate that was pre-coated with an antibody to DNA:RNA hybrids. After washing steps and detection of antibody-bound DNA:RNA hybrids by Streptavidin-peroxidase, the peroxidase activity of each well was tested.
The miRNAs miR-7, miR-380 and miR-1254 were used as the targeted nucleic acids of interest. Each miRNA was hybridized with three different nucleic acid probes specific to the respective miRNA of interest. Hybridization was performed at varying temperatures as indicated in table 2 below. As control, the miRNA was also incubated with a non-specific nucleic acid probe under identical hybridization conditions. The nucleic acid probes were labelled with biotin.
The miRNAs were diluted to 100 pmol/μI in a suitable storage buffer (such as Tris HCl/EDTA (TE) buffer) and synthetic DNA oligonucleotides were diluted to 100 pmol/μI in 1× TrisHCl saline buffer (TBS). 30 μl RNA solution and 30 μl DNA solution were incubated for 2 min at 95° C. to dissolve secondary structures and then hybridized at 40-65° C. After that, hybrids could be used immediately or frozen (e.g. at −20° C.) and stored for later use.
The sequences for the nucleic acid probes and miRNAs are given in the table 1 below:
ELISA plates were pre-coated with an anti-DNA: RNA-Hybrid antibody under standard conditions (5 yg/ml in phosphate-buffered saline (PBS)). After coating, the ELISA plates were washed with a commercially available wash solution or a TRIS/citric acid buffer.
The hybrids were diluted 1:100, 1:1000, 1:10000 and 1:100000 in:
PBS,
PBS with 1 yg/ml BSA and 0.1 yg/ml Tween 20,
PBS with 0.5 yg/ml BSA and 0.05 yg/ml Tween 20, or
PBS with 0.25 yg/ml BSA and 0.025 yg/ml Tween 20, respectively and incubated on coated ELISA plates for 1 hr at 37° C. After incubation plates were washed and incubated with a commercially available Streptavidine POD conjugate. Plates were washed and a chromogenic substrate (tetramethyl benzidine) solution was added to the plates. Color development was stopped by addition of a sulphuric acid stop solution and optical density (OD) was read at 450 nm. Results for 1:100000 dilutions of hybrids 1 to 12 are given in table 2, below.
As can easily be seen from the results shown in table 2, the method of the invention allows for an accurate, sensitive, specific and reproducible detection of miRNAs.
All full complementary DNA:RNA hybrids tested resulted in ODs>>1, whereas unspecific DNA:RNA hybrids or buffer alone resulted in ODs<<0.1. The OD values for non-specific controls (i.e. hybrids 4, 8 and 12) were in the same order of magnitude as zero values obtained with only PBS instead of a hybrid sample. It has thus been shown for the first time that miRNAs can be detected with high sensitivity and specificity by an immunoassay method. The assay described in the above example has been repeatedly performed with varying combinations of buffers and washing solutions, all with comparable results, thus demonstrating a robust, reproducible method of detecting miRNAs. Dilution series show a good detection over several orders of magnitude with high linearity and reproducibility.
The ELISA assay format as used e.g. in the above example is known to be well suited for a quantitative detection of analytes as well.
| Number | Date | Country | Kind |
|---|---|---|---|
| 12159196.0 | Mar 2012 | EP | regional |
This application is the national phase under 35 U.S.C. §371 of PCT International Application No. PCT/EP2013/054745 which has an International filing date of 8 Mar. 2013, which designated the United States of America, and which claims priority to European patent application number EP 12159196.0 filed 13 Mar. 2012, the entire contents of each of which are hereby incorporated herein by reference.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2013/054745 | 3/8/2013 | WO | 00 |
