Cyanine dyes
The invention provides a novel class of cyanine dyes that are functionalized with sulfonic acid groups and a linker moiety that facilitates their conjugation to other species and substituent groups which increase the water-solubility, and optimize the optical properties of the dyes. Also provided are conjugates of the dyes, methods of using the dyes and their conjugates and kits including the dyes and their conjugates.
1. A cyanine compound or conjugate having the structure of Formula (I) or (II):
wherein
n is an integer selected from 1, 2, and 3;
a, e, and j are independently selected from the integers 1, 2, 3, and 4, such that when a is 2 or greater, each R a is independently selected, when e is 2 or greater, each R e is independently selected, and when j is 2 or greater, each R j is independently selected;
b and e′ are independently selected from the integers 0, 1, and 2, such that when b is 2, each R b is independently selected, and when e′ is 2, each R e′ is independently selected;
R a , R b , R e , R e′ , and R j , are independently selected from C(O)R 9 , OR 12 , NR 12 R 13 , CR 12 C(O)R 13 , NR 12 C(O) 2 R 13 , SO 3 H, and C(O)NR 12 R 13 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, and a bond to M;
R f , R g , R h , and R i are members independently selected from halogen, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl and substituted or unsubstituted heteroalkyl, and a bond to M;
R c , and R d are independently selected from a bond to M, and alkyl substituted with a member selected from sulfonic acid, carboxylic acid, phosphonic acid, and phosphoric acid, and heteroalkyl substituted with a member selected from sulfonic acid, carboxylic acid, phosphonic acid, and phosphoric acid;
wherein
R 9 is a member selected from OR 10 , and a bond to M;
R 10 is a member selected from H and substituted or unsubstituted alkyl; and
R 12 and R 13 are members independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, and a bond to M,
wherein
M comprises a linker bound to a carrier molecule.
2. The cyanine compound or conjugate according to claim 1 , wherein said linker bound to a carrier molecule is a linker bound to a moiety having the structure of Formula III:
wherein
u is an integer selected from 1, 2, 3, 4, 5, 6, 7 and 8;
r is 0 or 1; and
Y is a nucleobase.
3. The cyanine compound or conjugate according to claim 1 , said compound or conjugate having the structure of Formula IV:
4. The cyanine compound or conjugate according to claim 1 , said compound or conjugate having the structure of Formula V:
5. The cyanine compound or conjugate according to claim 1 , said compound or conjugate having the structure of Formula VI:
6. The cyanine compound or conjugate of claim 1 , comprising at least one M moiety, wherein the linker of this moiety comprises the structure C(O)NH(CH 2 ) t , wherein the index t is an integer selected from 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, and 12.
7. The cyanine compound or conjugate of claim 1 , comprising at least one M moiety, wherein said linker of this moiety comprises a polyvalent scaffold.
8. The cyanine compound or conjugate according to claim 7 , wherein said polyvalent scaffold is a polyvalent arylene scaffold.
9. The cyanine compound or conjugate of claim 7 , wherein the polyvalent scaffold comprises a second cyanine moiety bound thereto, said second cyanine moiety having a structure according to Formula I or Formula II.
10. The cyanine compound or conjugate of claim 1 , comprising at least one M, wherein the linker comprises biotin bound to streptavidin.
11. The cyanine compound or conjugate according to claim 1 , wherein said cyanine compound or conjugate has a structure selected from the following formulae:
12. The cyanine compound according to claim 1 , wherein the linker of the M moiety includes a —C(O)—.
13. The cyanine compound or conjugate according to claim 2 , having a structure selected from the following formulae:
14. The cyanine compound or conjugate according to claim 1 , having the formula:
M-(R D ) 2
wherein
each R D has a structure independently selected from Formula I and Formula II.
15. The cyanine compound or conjugate according to claim 7 , wherein M comprises the polyvalent arylene scaffold moiety:
16. The cyanine compound or conjugate according to claim 13 , having the formula:
wherein
each R D has a structure independently selected from Formula I and Formula II.
17. The cyanine compound or conjugate according to claim 2 , having at least one Y moiety comprising a natural nucleobase.
18. The cyanine compound or conjugate according to claim 1 , wherein the carrier molecule comprises a member selected from a nucleic acid, a protein, a glycoprotein, a peptide, a saccharide, a hormone, a receptor, an antigen, a substrate, metabolite, a transition state analog, a cofactor, an inhibitor, a drug, a dye, a nutrient, and a growth factor.
19. The cyanine compound or conjugate according to claim 1 , wherein the carrier molecule comprises a member selected from a solid support, a virus and a microorganism.
20. A method of monitoring an enzyme reaction, said method comprising:
(a) forming a reaction mixture by contacting said enzyme with a cyanine compound or conjugate according to claim 1 , wherein said cyanine compound or conjugate is a substrate for said enzyme under conditions sufficient for said enzyme and said cyanine compound or conjugate to react; and
(b) monitoring fluorescence of said reaction mixture, thereby monitoring said enzyme reaction.
21. The method according to claim 20 , wherein said enzyme is a DNA polymerase and said cyanine compound or conjugate comprises a nucleic acid moiety, which is said substrate for said enzyme.
22. The method according to claim 20 , wherein said enzyme reaction is template directed DNA synthesis.
23. The method according to claim 20 , wherein said reaction is a component of a single molecule DNA sequencing analysis.
24. A cyanine compound or conjugate having the structure of Formula (I) or (II):
wherein
n is an integer selected from 1, 2, and 3;
a is selected from the integers 2, 3 and 4, and each R a is independently selected;
e, and j are independently selected from the integers 1, 2, 3, and 4, such that when e is 2 or greater, each R e is independently selected, and when j is 2 or greater, each R j is independently selected;
b and e′ are independently selected from the integers 0, 1, and 2, such that when b is 2, each R b is independently selected, and when e′ is 2, each R e′ is independently selected;
R a , R b , R e , R e′ , and R j , are independently selected from C(O)R 9 , OR 12 , NR 12 R 13 , CR 12 C(O)R 13 , NR 12 C(O) 2 R 13 , SO 3 H, and C(O)NR 12 R 13 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, and a bond to M;
R f , R g , R h , and R i are members independently selected from halogen, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl and substituted or unsubstituted heteroalkyl, and a bond to M;
R c , and R d are independently selected from a bond to M, and alkyl substituted with a member selected from sulfonic acid, carboxylic acid, phosphonic acid, and phosphoric acid, and heteroalkyl substituted with a member selected from sulfonic acid, carboxylic acid, phosphonic acid, and phosphoric acid;
wherein
R 9 is a member selected from OR 10 , and a bond to M;
R 10 is a member selected from H and substituted or unsubstituted alkyl; and
R 12 and R 13 are members independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, and a bond to M,
wherein
M comprises a linker bound to a carrier molecule.
25. A cyanine compound or conjugate having the structure of Formula (I) or (II):
wherein
n is an integer selected from 1, 2, and 3;
a, e, and j are independently selected from the integers 1, 2, 3, and 4, such that when a is 2 or greater, each R a is independently selected, when e is 2 or greater, each R e is independently selected, and when j is 2 or greater, each R j is independently selected, and at least one of R a , R b , R e and Rj is:
in which each Z is independently selected from SO 3 H and CO 2 H, each x is an integer independently selected from 0, 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10, and each R N is independently selected from H, and substituted or unsubstituted alkyl;
b and e′ are independently selected from the integers 0, 1, and 2, such that when b is 2, each R b is independently selected, and when e′ is 2, each R e′ is independently selected;
R a , R b , R e , R e′ , and R j , are independently selected from C(O)R 9 , OR 12 , NR 12 R 13 , CR 12 C(O)R 13 , NR 12 C(O) 2 R 13 , SO 3 H, and C(O)NR 12 R 13 , substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, and a bond to M;
R f , R g , R h , and R i are members independently selected from halogen, substituted or unsubstituted alkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl and substituted or unsubstituted heteroalkyl, and a bond to M;
R c , and R d are independently selected from a bond to M, and alkyl substituted with a member selected from sulfonic acid, carboxylic acid, phosphonic acid, and phosphoric acid, and heteroalkyl substituted with a member selected from sulfonic acid, carboxylic acid, phosphonic acid, and phosphoric acid;
wherein
R 9 is a member selected from OR 10 , and a bond to M;
R 10 is a member selected from H and substituted or unsubstituted alkyl; and
R 12 and R 13 are members independently selected from H, substituted or unsubstituted alkyl, substituted or unsubstituted heteroalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, substituted or unsubstituted heterocycloalkyl, and a bond to M,
wherein
M comprises a linker bound to a carrier molecule.