Use of Nucleic Acid Probes to Detect Nucleotide Sequences of Interest in a Sample
The invention relates to methods for the determination and detection of nucleic acids sequences in a sample. The nucleic acid may be RNA or DNA or both. The invention also relates to methods for the determination of the presence and species of various microorganisms in a sample. We have also identified a set of oligonucleotide nucleic acid sequences within the rRNAs of Gram-negative organisms that facilitates both the broad identification of Gram-negative organisms as a class when used as a pool, or in combination, for example in a hybridization assay. This set of oligonucleotides may detect sequences that are indicative of the presence of organisms of the broad class of Gram-negative organisms while exhibiting little or no false identification of Gram-positive organisms, and fungi, or other microorganisms. The assay includes concurrent incubation with at least one nucleotide sequence of interest, at least one nucleic acid probe, a fluorosurfactant, and a nuclease. The assay may further be employed to detect the presence of bacteria, fungi, or other microorganisms by use of additional specific probes, or to detect and/or identify target nucleic acid sequences in a sample. Further, the invention also relates to methods of reducing non-specific binding and facilitating complex formation in a binding assay. The binding assay may be, but is not limited to, a nucleic acid hybridization assay or an immunoassay. The invention also relates to methods of detection that employ at least one target of interest, which may be a nucleotide sequence, at least one probe, which may be a nucleic acid probe and a nuclease.
1 . A method of detecting the presence of at least one nucleotide sequence of interest in a sample comprising:
a) providing a sample potentially containing at least one nucleotide sequence of interest;
b) creating a mixture by combining:
i) the sample,
ii) at least one nucleic acid probe labeled with a detectable label, and
iii) a nuclease capable of degrading the sequence of interest;
wherein the nuclease is added to the sample before or concurrently with adding the probe;
wherein a complex forms between the sequence of interest and the probe; and
c) measuring the level of the detectable label in the complex, wherein the presence of the detectable label in the complex indicates the presence of the sequence of interest.
2 . A method of detecting the presence of at least one nucleotide sequence of interest in a sample comprising:
a) providing a sample potentially containing at least one nucleotide sequence of interest;
b) creating a mixture by combining:
i) the sample, and
ii) a combination of at least one nucleic acid probe labeled with a detectable label, and a nuclease capable of degrading the sequence of interest; wherein a complex forms between the sequence of interest and the probe; and
c) measuring the level of the detectable label in the complex, wherein the presence of the detectable label in the complex indicates the presence of the sequence of interest.
3 . A method of detecting the presence of at least one nucleotide sequence of interest in a sample comprising:
a) providing a sample potentially containing at least one nucleotide sequence of interest;
b) creating a mixture by combining:
i) the sample,
ii) at least one nucleic acid probe labeled with a detectable label, and
iii) a nuclease capable of degrading the sequence of interest;
wherein the probe is added to the sample within a selected time period;
wherein a complex forms between the sequence of interest and the probe; and
c) measuring the level of the detectable label in the complex, wherein the presence of the detectable label in the complex indicates the presence of the sequence of interest.
4 . The method according to claim 3 , wherein the selected time period is from about 0 to about 15 minutes after addition of the nuclease.
5 . A method of detecting the presence of at least one nucleotide sequence of interest in a sample comprising:
a) providing a sample potentially containing at least one nucleotide sequence of interest;
b) creating a mixture by combining:
i) the sample,
ii) at least one nucleic acid probe labeled with a detectable label, and
iii) a nuclease capable of degrading the sequence of interest;
wherein the nuclease is added to the sample and the probe before the sequence of interest hybridizes to the probe, resulting in a selected percentage of hybridization;
wherein a complex forms between the sequence of interest and the probe; and
c) measuring the level of the detectable label in the complex, wherein the presence of the detectable label in the complex indicates the presence of the sequence of interest.
6 . The method of claim 5 , wherein the selected percentage of hybridization is from about 5% to about 95%.
7 . A method of detecting the presence of at least one nucleotide sequence of interest in a sample comprising:
a) providing a sample potentially containing at least one nucleotide sequence of interest;
b) creating a mixture by combining:
i) the sample,
ii) at least one nucleic acid probe labeled with a detectable label, and
iii) a nuclease capable of degrading the sequence of interest; and
iv) at least one fluorosurfactant;
wherein a complex forms between the sequence of interest and the probe; and
c) measuring the level of the detectable label in the complex, wherein the presence of the detectable label in the complex indicates the presence of the sequence of interest.
8 . The method according to claim 7 , wherein the fluorosurfactant is selected from the group of an anionic fluorosurfactants, cationic fluorosurfactants, amphoteric fluorosurfactants, nonionic fluorosurfactants, zwitterionic fluorosurfactants, and mixtures thereof.
9 . The method according to any of claims 1 , 2 , 3 , or 5 , further comprising adding at least one fluorosurfactant to the mixture.
10 . The method according to claim 9 , wherein the at least one fluorosurfactant is selected from the group consisting of anionic fluorosurfactants, cationic fluorosurfactants, amphoteric fluorosurfactants, nonionic fluorosurfactants, zwitterionic fluorosurfactants, and mixtures thereof.
11 . The method according to any of claims 1 , 2 , 3 , 5 , or 7 , further comprising extracting the nucleotide sequence of interest from the sample before creating the mixture.
12 . The method according to any of claims 1 , 2 , 3 , 5 , or 7 , wherein the nuclease is selected from the group consisting of RNase A, RNase T1, RNase I, and S1 nuclease.
13 . The method according to any of claims 1 , 2 , 3 , 5 , or 7 , wherein the complex is immobilized.
14 . The method according to claim 13 , further comprising washing the complex with a wash buffer.
15 . The method according to any of claims 1 , 2 , 3 , 5 , or 7 , further comprising adding a reagent substrate to the complex.
16 . The method according to any of claims 1 , 2 , 3 , 5 , or 7 , wherein the probe comprises a capture probe labeled with biotin and a signal probe labeled with alkaline phosphatase.
17 . The method according to claim 16 , further comprises adding a reagent substrate to the complex, wherein the reagent substrate is selected from the group consisting of adamantyl-1,2-dioxetane phosphate, 5-bromo-4-chloro-3-indolyl phosphate/nitro blue tetrazolium and para-nitrophenyl phosphate.
18 . A kit comprising:
a) at least one nucleic acid probe labeled with a detectable label;
b) at least one fluorosurfactant; and
c) a nuclease capable of degrading a nucleotide sequence of interest.
19 . The kit of claim 18 , further comprising instructions for using the kit.
20 . The kit of claim 18 , further comprising a substrate reagent.
21 . A method of detecting the presence of a target of interest in a sample comprising:
a) providing a sample potentially containing a target of interest;
b) creating a mixture by combining:
i) the sample;
ii) at least one probe labeled with a detectable label; and
iii) at least one fluorosurfactant;
wherein a complex forms between the target of interest and the probe; and
c) measuring the level of the detectable label in the complex, wherein the presence of the detectable label in the complex indicates the presence of the target of interest.
22 . The method of claim 21 , wherein the at least one fluorosurfactant is selected from the group consisting of anionic fluorosurfactants, cationic fluorosurfactants, amphoteric fluorosurfactants, nonionic fluorosurfactants, zwitterionic fluorosurfactants, and mixtures thereof.
23 . The method of claim 21 , wherein the target of interest is selected from the group consisting of proteins, peptides, small chemical molecules, carbohydrates, lipopolysaccharides, polysaccharides, and lipids.
24 . A method of reducing non-specific binding of cells, subcellular organelles, biomolecules, or chemical molecules comprising:
a) adding at least one fluorosurfactant to a buffer; and
b) contacting the cells, subcellular organelles, biomolecules or chemical molecules with the buffer;
wherein the presence of the at least one fluorosurfactant results in the reduction of non-specific binding of the cells, subcellular organelles, biomolecules or chemical molecules to a surface or to each other.
25 . The method of claim 24 , wherein the at least one fluorosurfactant is selected from the group consisting of anionic fluorosurfactants, cationic fluorosurfactants, amphoteric fluorosurfactants, nonionic fluorosurfactants, zwitterionic fluorosurfactants, and mixtures thereof.
26 . The method of claim 24 , wherein the application is selected from the group consisting of an immunoassay, a microfluidic assay, passivation of a vessel surface, and cell culture.