Method of detection of nucleic acids with a specific sequence composition

• US 8,114,962 B2
• Filed: 06/29/2009
• Issued: 02/14/2012
• Est. Priority Date: 12/09/1994
• Status: Expired due to Fees

• Current Assignee: Gene Pool, Inc.
• Original Assignee: Gene Pool, Inc.
• Inventors: Weininger, Susan, Weininger, Arthur M.
• Primary Examiner(s): Brusca, John S
• Application Number:
  US12/493,877
• Publication Number:
  US 20100113344A1
• Time in Patent Office: 960 Days
• Field of Search: None
• US Class Current: 530/358
• CPC Class Codes: A61P 31/14 for RNA viruses
• CPC Class Codes: A61P 31/18 for HIV
• CPC Class Codes: C12Q 1/6804 Nucleic acid analysis using immunogens immunoassay G01N33/53
• CPC Class Codes: C12Q 1/6811 Selection methods for production or design of target specific oligonucleotides or binding molecules
• CPC Class Codes: C12Q 1/6813 Hybridisation assays
• CPC Class Codes: C12Q 1/682 Signal amplification
• CPC Class Codes: C12Q 1/6827 for detection of mutation or polymorphism
• CPC Class Codes: C12Q 1/6853 using modified primers or templates
• CPC Class Codes: C12Q 1/703 Viruses associated with AIDS
• CPC Class Codes: C12Q 1/708 for papilloma
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides
• CPC Class Codes: C12Q 2537/143 Multiplexing, i.e. use of multiple primers or probes in a single reaction, usually for simultaneously analyse of multiple analysis
• CPC Class Codes: C12Q 2537/149 Sequential reactions
• CPC Class Codes: C12Q 2537/161 A competitive reaction step

Abstract

This invention is a novel method for detecting and localizing specific nucleic acid sequences in a sample with a high degree of sensitivity and specificity. The method and novel compositions used in the method involve the use of Probe Nucleic Acids, the production of nucleic acid binding regions and the use of nucleic acid Target Binding Assemblies to detect and localize specific Target Nucleic Acids. The detection and localization of the Target Nucleic Acid is accomplished even in the presence of nucleic acids which have similar sequences. The method provides for a high degree of amplification of the signal produced by each specific binding event. In particular, methods and compositions are presented for the detection of HIV and HPV nucleic acid in samples. These methods and compositions find use in diagnosis of disease, genetic monitoring, forensics, and analysis of nucleic acid mixtures. Some of the novel compositions used in the detection method are useful in preventing or treating pathogenic conditions.

Claims

1. An isolated target binding assembly (TBA) comprising a first and a second nucleic acid recognition unit, wherein:

said first nucleic acid recognition unit is capable of binding with specificity to a first target nucleotide sequence contained within a target polynucleotide;

said second nucleic acid recognition unit is capable of binding with specificity to a second target nucleotide sequence contained within a target polynucleotide;

said nucleic acid recognition units are polypeptides and are the same or different; and

wherein said TBA comprises a sequence selected from the group consisting of;

A. I+II+III;

B. IV+V+III; and

C. IV+III;

wherein

I indicates any of SEQ ID NOS;

85-92;

II indicates Met Ser, linked to any of SEQ ID NOS;

104-106, each of which is linked to SEQ ID NO;

99;

III indicates SEQ ID NO;

100 linked to any of SEQ ID NOS;

75-84 or 94-98;

SEQ ID NO;

101 linked to either SEQ ID NO;

74 or SEQ ID NO;

93;

or SEQ ID NO;

102 linked to SEQ ID NO;

74 or SEQ ID NO;

93;

or any of SEQ ID NOS;

72, 103, 73, or 63-71;

IV indicates any of SEQ ID NOS. 104-106; and

V indicates SEQ ID NO;

99.

2. The TBA of claim 1, wherein each said target nucleotide sequence includes at least 7 contiguous nucleotides.

3. The TBA of claim 1, wherein said first nucleic acid recognition unit is capable of binding said first target nucleotide sequence at the same time that said second nucleic acid recognition unit is bound to said second target nucleotide sequence, when said first and second target nucleotide sequences:

are both contained within the same target polynucleotide; and

are separated from one another by intervening nucleotide(s).

4. The TBA of claim 3, wherein each said target nucleotide sequence includes at least 7 contiguous nucleotides.

5. The TBA of claim 2, wherein said first and second nucleic acid recognition units are DNA-binding polypeptides.

6. The TBA of claim 3, wherein said first and second nucleic acid recognition units are DNA-binding polypeptides.

7. The TBA of claim 4, wherein said first and second nucleic acid recognition units are DNA-binding polypeptides that bind reversibly and non-covalently to double-stranded DNA.

8. The TBA of claim 7, wherein said first and second nucleic acid recognition units, when considered separately, each have a binding affinity K_d for their respective target nucleotide sequence that is numerically greater than 10⁻

6 M.

9. A composition comprising the TBA of claim 1 bound to a target polynucleotide comprising said first target nucleotide sequence and said second target nucleotide sequence, whereby transcription of a gene contained within the target polynucleotide is hindered.