Polymer dye modification and applications
Water-soluble photoactive polymers, included polymer tandem dyes, as described as well as methods for their preparation and use. The photoactive polymers can be prepared by direct modification of core polymers (e.g., violet excitable polymers) with dyes or other functional groups. Methods of detecting analytes using the polymers are also described.
1. A conjugated polymer according to Formula I:
wherein:
each A is independently selected from the group consisting of an aromatic co-monomer and a heteroaromatic co-monomer;
L 1 comprises a sulfonamide, a sulfinamide, a disulfonamide, a disulfinamide, a sultam, an amide, a secondary amine, a phosphonamide, a phosphinamide, a phosphonamidate, a selenonamide, or a seleninamide; L 2 and L 3 are linker moieties;
W is a water-solubilizing moiety;
each E is an independently selected chromophore, functional moiety, or binding agent;
each B is independently selected from the group consisting of an aromatic co-monomer, a heteroaromatic co-monomer, a bandgap-modifying monomer, optionally substituted eth lene, and optionally substituted ethynylene;
G 1 and G 2 are independently selected from an unmodified polymer terminus and a modified polymer terminus, wherein one or both of G 1 and G 2 are modified with a capping moiety;
subscripts n and m are independently integers ranging from 1 to 10,000,
subscript p is an integer ranging from 0 to 10,000, and
the sum of subscripts n, m, and p ranges from 2 to 10,000;
subscript q is 1, 2, 3, or 4;
subscript r is 1, 2, 3, or 4;
subscript s is 0, 1, 2, or 3;
subscript t is 1 or 2
the sum of subscript r and s ranges from 1 to 4; and
A and B are distributed randomly or non-randomly in the conjugated polymer, wherein the functional moiety is a biotin, digoxigenin, a peptide tag, an oligonucleotide, or a polynucleotide, and the binding agent is a molecule or complex of molecules capable of specific binding to a target analyte, wherein the binding agent is selected from the group consisting of protein, antibody, antibody fragment, carbohydrate, polysaccharide, oligonucleotide, polynucleotide, lipid, affinity ligand, and aptamer.
2. The conjugated polymer of claim 1 , wherein L 3 is a bond.
3. The conjugated polymer of claim 1 , wherein:
subscript q is equal to the sum of subscripts r and s,
subscript r is 1 or 2,
if subscript r is 1, then subscript s is 0 or 1, and
if subscript r is 2, then subscript s is 0.
4. The conjugated polymer of claim 1 , having a structure according to Formula II:
wherein:
L 1a is a linker moiety; and
R 1 is selected from the group consisting of H and an amine protecting group.
5. The conjugated polymer of claim 4 , wherein:
L 1a is selected from the group consisting of a covalent bond, C 1-8 alkylene, 2- to 8-membered heteroalkylene, —NHC(O)L a —, —C(O)NHL a —, and —C(O)L a —;
L 2 is selected from the group consisting of a covalent bond, C 1-8 alkylene; 2- to 8-membered heteroalkylene, —L b NHC(O)—, —L b C(O)NH—, —L b C(O)—, —C(O)NHL b —, and —C(O)L b —; and
L a and L b are independently selected from the group consisting of C 1-8 alkylene and 2- to 8-membered heteroalkylene.
6. The conjugated polymer of claim 1 , wherein W comprises one or more ethylene glycol monomers.
7. The conjugated polymer of claim 1 , wherein W comprises poly(ethylene glycol).
8. The conjugated polymer of claim 1 , wherein each A is the same co-monomer.
9. The conjugated polymer of claim 1 , wherein A is a violet fluorescent monomer.
10. The conjugated polymer of claim 1 , wherein A is a 9,10-phenanthrenedione-based monomer, a dihydrophenanthrene-based monomer, a dihydrophcnanthrene oxepine-based monomer, a fluorene-based monomer, or a fluorenooxepine-based monomer.
11. The conjugated polymer of claim 1 , having a structure according to Formula III:
wherein each subscript t is an integer ranging from 1 to 20.
12. The conjugated polymer of claim 1 , wherein one or both of G 1 and G 2 modified with a capping moiety is covalently bonded to a binding agent or a substrate material.
13. The conjugated polymer of claim 1 , wherein one of G 1 and G 2 is modified with a capping moiety, and one of G 1 and G 2 is modified with reactive functional group.
14. The conjugated polymer of claim 1 , wherein each E is an independently selected chromophore.
15. A method of making a conjugated polymer according to Formula II:
the method comprising converting a conjugated polymer according to Formula IIa:
to the polymer according to Formula II, wherein:
A is a fluorescent monomer;
L 1a and L 2 are linker moieties;
W is a water-solubilizing moiety;
each E is an independently selected chromophore;
each B is independently selected from the group consisting of an aromatic co-monomer, a heteroaromatic co-monomer, a bandgap-modifying monomer, optionally substituted ethylene, and optionally substituted ethynylene;
G 1 and G 2 are independently selected from an unmodified polymer terminus and a modified polymer terminus, wherein one or both of G 1 and G 2 are modified with a capping moiety;
R 1 is selected from the group consisting of H and an amine protecting group;
subscripts n and in are independently integers ranging from 1 to 10,000,
subscript p is an integer ranging from 0 to 10,000, and
the sum of subscripts n, m, and p ranges from 2 to 10,000;
subscript q is 1, 2, 3, or 4;
subscript r is 1, 2, 3, or 4;
subscript s is 0, 1, 2, or 3;
subscript t is 1 or 2
the sum of subscript r and s ranges from 1 to 4; and
A and B are distributed randomly or non-randomly in the fluorescent polymer.