Methods employing oligonucleotide-binding e-tag probes

• US 6,686,152 B2
• Filed: 04/02/2001
• Issued: 02/03/2004
• Est. Priority Date: 04/30/1999
• Status: Expired due to Fees

• Current Assignee: Monogram Biosciences, Inc. (Laboratory Corporation Of America Holdings)
• Original Assignee: Aclara Biosciences, Inc (Laboratory Corporation Of America Holdings)
• Inventors: Tian, Huan, Singh, Sharat
• Primary Examiner(s): Siew, Jeffrey
• Assistant Examiner(s): Tung, Joyce
• Application Number:
  US09/825,247
• Publication Number:
  US 20020001808A1
• Time in Patent Office: 1,037 Days
• Field of Search: 435/6, 435/91.2, 536/24.2, 536/24.31, 536/23.1, 536/24.33, 536/25.32, 536/26.6
• US Class Current: 435/6.16
• CPC Class Codes: C07H 19/06 Pyrimidine radicals
• CPC Class Codes: C07H 19/10 with the saccharide radical esterified by phosphoric or polyphosphoric acids
• CPC Class Codes: C07H 21/00 Compounds containing two or more mononucleotide units having separate phosphate or polyphosphate groups linked by saccharide radicals of nucleoside groups, e.g. nucleic acids
• CPC Class Codes: C40B 70/00 Tags or labels specially adapted for combinatorial chemistry or libraries, e.g. fluorescent tags or bar codes
• CPC Class Codes: G01N 33/561 Immunoelectrophoresis
• CPC Class Codes: Y10S 435/81 Packaged device or kit

Abstract

Methods for the multiplexed detection of known, selected nucleotide target sequences are provided. Detection involves the release of identifying tags as a consequence of target recognition. The methods include the use of electrophoretic tag probes or e-tag probes, comprising a detection region and a mobility-defining region called the mobility modifier, both linked to a target-binding moiety. In practicing the methods, the target-binding moiety of the e-tag probes hybridizes to complementary target sequences followed by nuclease cleavage of the e-tag probes and release of detectable e-tags or e-tag reporters. The mixture is exposed to a capture agent which binds uncleaved and/or partially cleaved e-tag probes, followed by electrophoretic separation. In a multiplexed assay, different released e-tag reporters may be separated and detected providing for target identification.

Claims

1. A method of detecting the presence or absence of each of a plurality of polynucleotides in a sample, the method comprising the steps of:

providing for each polynucleotide a primer specific for a first region of the polynucleotide and an electrophoretic probe specific for a second region of the polynucleotide, the electrophoretic probe having a capture ligand attached and an eTag reporter attached, such that the eTag reporter of each electrophoretic probe has an electrophoretic mobility different from that of the eTag reporters of every other electrophoretic probe so that eTag reporters from different electrophoretic probes form distinct peaks in an electropherogram upon electrophoretic separation;

combining in a mixture a nuclease, the sample, the electrophoretic probes, and the primers under conditions that allow the primers and the electrophoretic probes to hybridize to their respective polynucleotides to form complexes, the nuclease recognizing such complexes and digesting the electrophoretic probes therein so that eTag reporters are released;

excluding from the electropherogram undigested electrophoretic probes by treating the mixture with a capture agent that specifically binds the capture ligands of the electrophoretic probes; and

electrophoretically separating and identifying the released eTag reporters to determine the presence or absence of each of the plurality of polynucleotides.

2. The method of claim 1 wherein said electrophoretic tag has a molecular weight of from 150 to 10,000 daltons.

10. The method of claim 1 wherein each of said electrophoretic probes is defined by the formula:

11. The method of claim 10 wherein:

(i) D is a fluorescent label, (ii) said capture ligand is biotin and said capture agent is avidin or streptavidin, (iii) M is a mobility modifier having a molecular weight in the range of from 35 to 1500 daltons, and (iv) said plurality of said polynucleotides is in the range of from 5 to 100.

3. The method according to 2 wherein each of said electrophoretic probes is defined by the formula:

4. The method of claim 3 wherein said plurality of said polynucleotides is in the range of from 5 to 100, and wherein said eTag reporter is defined by the formula:

5. The method of claim 4 wherein said fluorescent label is a fluorescein.

6. The method of claim 3 wherein said capture ligand is biotin and said capture agent is avidin or streptavidin.

7. The method of claim 3 wherein said capture ligand is an antigen and said capture agent is an antibody or antibody fragment that binds specifically to the antigen.

8. The method of claim 3 wherein said capture ligand is a polycation and said oligonucleotide, T, has a negatively charged backbone.

9. The method of claim 3 wherein T contains at least one nuclease-resistant intersubunit linkage.