Non-fluorescent quencher compounds and biomolecular assays
View Patent ↗Bis-diazo, triaryl and aryldiazo-N-arylphenazonium quencher moieties, substituted with electron-withdrawing and electron-donating substituents which induce polarity in the delocalized aryl/diazo ring systems, are useful as labels when attached to biomolecules such as polynucleotides, nucleosides, nucleotides and polypeptides. The quencher moieties are non-fluorescent and accept energy transfer from fluorescent reporter labels by any energy-transfer mechanism, such as FRET. Fluorescence quencher compositions are useful in preparing quencher labeled biomolecules for various molecular biology assays based on fluorescence detection.
1. A composition useful for synthesizing a quencher-labeled polynucleotide which has the structure (II):
wherein:
Q is a quencher moiety Q1 having the following structure:
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,
further wherein:
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
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; and
a reactive linking group linking the aryl carbon of the quencher moiety to L 1 , either directly or by way of a linker NR″R″ moiety, where each R″ is independently C 1 -C 12 alkyl;
L 1 , L 3 and L 4 are each, independently of one another, selected from a bond, C 1 -C 12 alkyldiyl, C 1 -C 12 alkoxyldiyl, C 1 -C 12 alkylaminodiyl, C 1 -C 12 alkylamidediyl, C 5 -C 14 aryldiyl, and 1-20 ethyleneoxy units;
L 2 is a C 1 -C 12 alkoxyldiyl, wherein the hydroxyl group is attached to X;
A is a cleavable linker;
X is an acid-labile protecting group;
Y is selected from N and CR, where R is selected from H, C 1 -C 6 alkyl, and C 5 -C 14 aryl; and
represents the solid support.
2. The composition of claim 1 , wherein 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, wherein each R′ is independently H, C 1 -C 12 alkyl or C 5 -C 14 aryl.
3. The composition of claim 1 , wherein the electron-donating groups are each, independently of one another, selected from O − , S − , NR″R″, NHR″, NH 2 , NHC(O)R″, OR″, OH, OC(O)R″, SR″, SH, Br, I, Cl, F, R″ and C 5 -C 14 aryl, wherein each R″ is independently H, C 1 -C 12 alkyl or C 5 -C 14 aryl.
4. The composition of claim 1 , wherein R 10 is NO 2 .
5. The composition of claim 1 , wherein at least one of R 1 , R 2 , R 3 , 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 .
6. The composition of claim 1 , wherein the reactive linking group comprises an electrophile.
7. The composition of claim 6 , wherein the electrophile of the reactive linking group is a carboxylic acid or an ester.
8. The composition of claim 1 , wherein one R″ is substituted C 1 -C 12 alkyl and the other R″ is unsubstituted C 1 -C 12 alkyl.
9. The composition of claim 8 , wherein the one R″ that is unsubstituted C 1 -C 12 alkyl is CH 2 CH 3 .
10. A compound having a structure of one of the following formulae:
11. A compound having a structure of one of the following formulae:
12. The composition of claim 1 , wherein A is selected from;
wherein R a is selected from H, C 1 -C 12 alkyl, and C 1 -C 12 alkoxy.
13. The composition of claim 1 , wherein X is selected from DMT, MMT, trityl, substituted trityl, pixyl, and trialkylsilyl.
14. The composition of claim 1 , wherein the solid support is selected from polystyrene, controlled-pore glass, silica gel, silica, polyacrylamide, polyacrylate, hydroxyethylmethycrylate, polyamide, polyethylene, polyethyleneoxy, and copolymers and grafts of such polymers.
15. A quencher-labeled conjugate, produced by reacting a phosphoramidite reagent of a nucleoside, a nucleotide or a polynucleotide with the alkoxydiyl L 2 moiety of the composition of claim 1 , after removal of the acid labile X moiety of the composition.
16. The quencher-labeled conjugate of claim 15 , wherein the conjugated substance is a polynucleotide comprising 2-100 nucleotides, and protected forms thereof.
17. The quencher-labeled conjugate of claim 16 , further comprising 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.
18. A method of attaching a nucleotide to the composition of claim 1 , comprising:
removing the acid labile protecting group X from the composition thereby forming a deprotected composition;
contacting the deprotected composition with a phosphoramidite nucleotide reagent, thereby forming a quencher labeled nucleotide.
19. A 3′ quencher polynucleotide bound to a solid support, having the structure:
wherein the polynucleotide comprises 2 to 100 nucleotides;
Q is a quencher moiety Q1 having the following structure:
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, further wherein:
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
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; and
a reactive linking group linking the aryl carbon of the quencher moiety to L 1 , either directly or by way of a linker NR″R″ moiety, where each R″ is independently C 1 -C 12 alkyl;
L 1 , L 3 and L 4 are each, independently of one another, selected from a bond, C 1 -C 12 alkyldiyl, C 1 -C 12 alkoxyldiyl, C 1 -C 12 alkylaminodiyl, C 1 -C 12 alkylamidediyl, C 5 -C 14 aryldiyl, and 1-20 ethyleneoxy units;
L 2 is a C 1 -C 12 alkoxyldiyl, wherein the hydroxyl group is attached to a phosphodiester moiety of a first nucleotide;
A is a cleavable linker;
Y is selected from N and CR, where R is selected from H, C 1 -C 6 alkyl, and C 5 -C 14 aryl; and
represents the solid support.
20. The 3′ quencher polynucleotide of claim 19 , wherein A is selected from;
wherein R a is selected from H, C 1 -C 12 alkyl, and C 1 -C 12 alkoxy.
21. The 3′ quencher polynucleotide of claim 19 , wherein 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, wherein each R′ is independently H, C 1 -C 12 alkyl or C 5 -C 14 aryl.
22. The 3′ quencher polynucleotide of claim 19 , wherein the electron-donating groups are each, independently of one another, selected from O − , S − , NR″R″, NHR″, NH 2 , NHC(O)R″, OR″, OH, OC(O)R″, SR″, SH, Br, I, Cl, F, R″ and C 5 -C 14 aryl, wherein each R″ is independently H, C 1 -C 12 alkyl or C 5 -C 14 aryl.
23. The 3′ quencher polynucleotide of claim 19 , wherein the reactive linking group comprises an electrophile.
24. The 3′ quencher polynucleotide of claim 19 , further comprising a fluorescent dye label.
25. A 5′ quencher polynucleotide bound to a solid support, having the structure:
wherein the polynucleotide comprises 2 to 100 nucleotides;
Q is a quencher moiety Q1 having the following structure:
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, further wherein:
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
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; and
a reactive linking group linking the aryl carbon of the quencher moiety to L 1 , either directly or by way of a linker NR″R″ moiety, where each R″ is independently C 1 -C 12 alkyl;
L 1 , L 3 and L 4 are each, independently of one another, selected from a bond, C 1 -C 12 alkyldiyl, C 1 -C 12 alkoxyldiyl, C 1 -C 12 alkylaminodiyl, C 1 -C 12 alkylamidediyl, C 5 -C 14 aryldiyl, and 1-20 ethyleneoxy units;
L 2 is a C 1 -C 12 alkoxyldiyl, wherein the hydroxyl group is attached to a phosphodiester moiety of a first nucleotide;
A is a cleavable linker;
Y is selected from N and CR, where R is selected from H, C 1 -C 6 alkyl, and C 5 -C 14 aryl; and
represents the solid support.
26. The 5′ quencher polynucleotide of claim 25 , wherein A is selected from;
wherein R a is selected from H, C 1 -C 12 alkyl, and C 1 -C 12 alkoxy.
27. The 5′ quencher polynucleotide of claim 25 , wherein 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, wherein each R′ is independently H, C 1 -C 12 alkyl or C 5 -C 14 aryl.
28. The 5′ quencher polynucleotide of claim 25 , wherein the electron-donating groups are each, independently of one another, selected from O − , S − , NR″R″, NHR″, NH 2 , NHC(O)R″, OR″, OH, OC(O)R″, SR″, SH, Br, I, Cl, F, R″ and C 5 -C 14 aryl, wherein each R″ is independently H, C 1 -C 12 alkyl or C 5 -C 14 aryl.
29. The 5′ quencher polynucleotide of claim 25 , wherein the reactive linking group comprises an electrophile.