Key probe compositions and methods for polynucleotide detection

• US 7,504,218 B2
• Filed: 02/09/2006
• Issued: 03/17/2009
• Est. Priority Date: 02/09/2005
• Status: Expired due to Fees

• Current Assignee: Stratagene California (Agilent Technologies, Inc.)
• Original Assignee: Stratagene California (Agilent Technologies, Inc.)
• Inventors: Happe, Scott B, Sorge, Joseph A, Firmin, Andrew
• Primary Examiner(s): WHISENANT, ETHAN C
• Application Number:
  US11/351,129
• Publication Number:
  US 20060292592A1
• Time in Patent Office: 1,132 Days
• Field of Search: 435/6, 536/23.1, 536/24.3
• US Class Current: 435/6.1
• CPC Class Codes: C12Q 1/6818 involving interaction of two or more labels, e.g. resonant energy transfer
• CPC Class Codes: C12Q 2525/301 Hairpin oligonucleotides

Abstract

The invention relates to compositions and methods for detection of nucleic acid sequences. The invention further relates to kit format of said compositions for detection of nucleic acid sequences. Oligonucleotide probes of the invention comprise a target binding sequence and a sequence at least partially complementary thereto, joined by an optional linker to form a hairpin structure in the absence of the target nucleic acid sequence. The probes of the invention comprise a pair of moieties that produce a detectable signal when the probe hybridizes to the target sequence.

Claims

1. A method of detecting a target nucleic acid sequence, comprising the steps of (1) incubating the target sequence with a probe capable of binding to a target nucleic acid sequence, said probe comprising (a) a first sequence which is at least partially complementary to a target sequence and has a stem portion and a loop portion, wherein the loop portion does not hybridize to the target sequence:

(b) a second sequence which is at least partially complementary to the stem portion of the first sequence;

(c) a first moiety operatively coupled to the first sequence; and

(d) a second moiety operatively coupled to the second sequence;

wherein the 3′

end of the first sequence is linked to the 5′

end of the second sequence;

wherein the stem portion of the first sequence and the second sequence are capable of hybridizing to each other when the probe is not hybridized to the target sequence; and

wherein hybridization of the probe to the target sequence causes either the first moiety or the second moiety to produce a detectable signal; and

(2) detecting a signal from the first or second moiety, wherein the step of incubating is performed in the presence of a nuclease.

2. The method of claim 1 wherein the nuclease is a flap endonuclease.

3. The method of claim 2 wherein a detectable signal is produced if the flap endonuclease performs an invasive cleavage.

4. The method of claim 2 wherein a detectable signal is produced if the flap endonuclease performs a non-invasive cleavage.

5. A method of detecting a target nucleic acid sequence, comprising the steps of (1) amplifying the target sequence using a polymerase chain reaction in the presence of a probe capable of binding to the target sequence, said probe comprising (a) a first sequence which is at least partially complementary to the target sequence and which consists of a stem portion and a loop portion, wherein the loop portion does not hybridize to the target sequence;

(b) a second sequence which is shorter than the first sequence and at least partially complementary to the stem portion of the first sequence; and

(c) first and second moieties;

wherein the 3′

end of the first sequence is linked to the 5′

end of the second sequence;

wherein the first sequence and the second sequence are capable of hybridizing to each other when the probe is not hybridized to the target sequence; and

wherein hybridization of the probe to the target sequence causes the first or second moiety to produce a detectable signal; and

(2) detecting a signal from the first or second moiety.

6. The method of claim 5 wherein the step of incubating amplifying is performed in the presence of a nuclease.

7. The method of claim 6 wherein the nuclease is a flap endonuclease.

8. The method of claim 7 wherein a detectable signal is produced if the flap endonuclease produces an invasive cleavage.

9. The method of claim 7 wherein a detectable signal is produced if the flap endonuclease produces a non-invasive cleavage.