IP Library Granted Patent US 8,633,307
Granted Patent B2
US 8,633,307 · App. 12/765,844 · Granted Jan 21, 2014

Dark quenchers for donor-acceptor energy transfer

Inventors: Ronald M. Cook (Novato, CA); Matt Lyttle (San Rafael, CA); Daren Dick (San Rafael, CA)
Assignee: Biosearch Technologies, Inc.
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Quick Facts
Patent No.
US 8,633,307
App. No.
12/765,844
Granted
Jan 21, 2014
Kind
B2
Abstract

The present invention provides a family of dark quenchers, termed Black Hole Quenchers (“BHQs”), that are efficient quenchers of excited state energy but which are themselves substantially non-fluorescent. Also provided are methods of using the BHQs, probes incorporating the BHQs and methods of using the probes.

Claims (29)

1. A quencher-labeled conjugate, comprising a quencher moiety and a conjugated substance, wherein the quencher moiety comprises structure (Q):

wherein:

at least one aryl carbon is substituted with an electron-withdrawing group; and

at least one aryl carbon is substituted with an electron-donating group,

and further wherein the quencher moiety is covalently linked to the conjugated substance at an aryl carbon, optionally by way of a linker; and

the conjugated substance is selected from an amino acid, a polypeptide, a nucleoside, a nucleotide, a polynucleotide and protected forms thereof.

2. The quencher-labeled conjugate of claim 1 in which the conjugated substance is a polynucleotide.

3. The quencher-labeled conjugate of claim 2 which further comprises a fluorescent moiety covalently attached to the polynucleotide, the fluorescence of which is capable of being quenched by the quencher moiety when the fluorescent and quencher moieties are in close proximity to one another.

4. The quencher-labeled conjugate of claim 3 in which the 3′-terminus of the polynucleotide cannot be extended by a polymerase.

5. The quencher-labeled conjugate of claim 4 in which the quencher moiety is attached to the 3′-terminal nucleotide of the polynucleotide and the fluorescent moiety is attached to the 5′-terminal nucleotide of the polynucleotide.

6. The quencher-labeled conjugate of claim 4 in which the quencher moiety is attached to the 3′-terminus of the polynucleotide.

7. The quencher-labeled conjugate of claim 4 in which the fluorescent moiety is attached to the 5′-terminus of the polynucleotide.

8. The quencher-labeled conjugate of claim 4 in which the fluorescent moiety is attached to the 3′-terminal nucleotide of the polynucleotide and the quencher moiety is attached to the 5′-terminal nucleotide of the polynucleotide.

9. The quencher-labeled conjugate of claim 4 in which the fluorescent moiety is attached to the 3′-terminus of the polynucleotide.

10. The quencher-labeled conjugate of claim 4 in which the quencher moiety is attached to the 5′-terminus of the polynucleotide.

11. A quencher-labeled conjugate, comprising a quencher moiety and a conjugated substance, wherein the quencher moiety comprises structure (Q):

wherein:

at least one aryl carbon is substituted with an electron-withdrawing group; and

at least one aryl carbon is substituted with an electron-donating group,

and further wherein the quencher moiety is covalently linked to the conjugated substance at an aryl carbon, optionally by way of a linker

in which the conjugated substance is a polypeptide.

12. The quencher-labeled conjugate of claim 1 in which the quencher moiety (Q) comprises structure (Q1):

wherein:

R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 and R 14 are each, independently of one another, selected from hydrogen, an electron-withdrawing group and an electron-donating group, or, alternatively R 4 may be taken together with R 5 or R 6 may be taken together with R 7 to form a benzo group,

with the provisos that: (i) at least one of R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 or R 14 is an electron-withdrawing group; and (ii) at least one of R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 or R 14 is an electron-donating group.

13. The quencher-labeled conjugate of claim 12 in which the electron-withdrawing groups are each, independently of one another, selected from NO 2 , CN, CF 3 , CO 2 H, CO 2 R′, C(O)NH 2 , N(O)NHR′, C(O)NR′R′, CHO, C(O)R′, SO 2 R′, SO 2 CF 3 , SO 2 OR′, SO 3 H, NO and C 5 -C 14 aryl, where R′ is H, C 1 -C 12 alkyl or C 5 -C 14 aryl.

14. The quencher-labeled conjugate of claim 12 in which R 10 is NO 2 .

15. The quencher-labeled conjugate of claim 12 in which at least one of R 1 , R 2 , R 4 , R 5 , R 6 , R 7 , R 8 , R 9 , R 10 , R 11 , R 12 , R 13 and R 14 is OCH 3 .

16. The quencher-labeled conjugate of claim 12 in which Q1 is selected from:

Assignments (4)
RELEASE OF SECURITY INTEREST IN PATENTS PREVIOUSLY RECORDED AT REEL/FRAME (035957/0976) Recorded Mar 8, 2016
From: HSBC CORPORATE TRUSTEE COMPANY (UK) LIMITED
To: BIOSEARCH TECHNOLOGIES, INC.
Reel/Frame 038037/0669 →
CORRECTIVE ASSIGNMENT TO CORRECT THE INCORRECT APPL. NO. 61/996,902 PREVIOUSLY RECORDED AT REEL: 035957 FRAME: 0976. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Aug 11, 2015
From: BIOSEARCH TECHNOLOGIES, INC.
To: HSBC CORPORATE TRUSTEE COMPANY (UK) LIMITED, AS SECURITY AGENT
Reel/Frame 036335/0516 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2015
From: BIOSEARCH TECHNOLOGIES, INC.
To: HSB CORPORATE TRUST COMPANY (UK) LIMITED, AS SECURITY AGENT
Reel/Frame 035957/0976 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 3, 2010
From: COOK, RONALD M.; LYTTLE, MATT; DICK, DAREN
To: BIOSEARCH TECHNOLOGIES, INC.
Reel/Frame 024481/0766 →
Continuity (5)
Continuation 12546927 · Aug 25, 2009
Continuation 11437991 · May 19, 2006
Division 11192705 · Jul 29, 2005
Continuation 09567863 · May 9, 2000
Related Publication 20110092679A1 · Apr 21, 2011