IP Library › Granted Patent US 11,209,438
Granted Patent B2
US 11,209,438 · App. 16/528,469 · Granted Dec 28, 2021

Fluorescent methods and materials for directed biomarker signal amplification

Inventors: Brent S. Gaylord (San Diego, CA); Janice W. Hong (San Diego, CA); Tsu-Ju Fu (Poway, CA); ChengJun Sun (Goleta, CA); Russell A. Baldocchi (Encinitas, CA)
Assignee: Becton, Dickinson and Company
G01N33/582C08G61/02C08G61/12G01N33/542C08G2261/3142C08G2261/3221C08G2261/3241C08G2261/3246C08G2261/522C08G2261/78C08G2261/94H01L51/0039Y10T436/13
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Quick Facts
Patent No.
US 11,209,438
App. No.
16/528,469
Granted
Dec 28, 2021
Kind
B2
Abstract

Methods and compositions are provided that include a multichromophore and/or multichromophore complex for identifying a target biomolecule. A sensor biomolecule, for example, an antibody can be covalently linked to the multichromophore. Additionally, a signaling chromophore can be covalently linked to the multichromophore. The arrangement is such that the signaling chromophore is capable of receiving energy from the multichromophore upon excitation of the multichromophore. Since the sensor biomolecule is capable of interacting with the target biomolecule, the multichromophore and/or multichromophore complex can provide enhanced detection signals for a target biomolecule.

Claims (45)

1. A multichromophore-biomolecule conjugate comprising:

a sensor biomolecule covalently linked to a light harvesting water soluble multichromophore via a bioconjugation site;

wherein the light harvesting water soluble multichromophore is a conjugated polymer having a backbone of π-conjugated repeat units and comprises the structure:

wherein:

CP 1 is present and is a fluorene repeat unit;

CP 2 is an aromatic repeat unit;

CP 3 is present and is an aromatic repeat unit comprising a bioconjugation functional group capable of covalently linking to a biomolecule or dye and that does not comprise a biotin group;

m is 1 to 10,0000;

n is independently 1 to 10,000 and; and

b is 0 to 250 and a and c are independently 1 to 250, wherein a+b+c>1.

2. The multichromophore-biomolecule conjugate according to claim 1 , wherein the multichromophore is substituted with a plurality of charge neutral water-soluble groups.

3. The multichromophore-biomolecule conjugate according to claim 1 , wherein CP 1 and CP 2 are each independently substituted with one or more water-soluble groups.

4. The multichromophore-biomolecule conjugate according to claim 1 , wherein the water-soluble groups comprise one or more groups selected from ethylene glycol oligomer, ethylene glycol polymer, ω-ammonium alkoxy salt and ω-sulfonate alkoxy salt.

5. The multichromophore-biomolecule conjugate according to claim 1 , wherein the sensor biomolecule is a protein, an antibody, a nucleic acid, an affinity ligand, a sugar, a lipid or a peptide.

6. The multichromophore-biomolecule conjugate according to claim 5 , wherein the sensor biomolecule is a protein, an antibody or a nucleic acid.

7. The multichromophore-biomolecule conjugate according to claim 6 , wherein the sensor biomolecule is an antibody.

8. The multichromophore-biomolecule conjugate according to claim 1 , wherein the bioconjugation site results from a linking chemistry selected from maleimide, thiol, succimidylester (NHS ester), amine, azide chemistry, carboxy/EDC (1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride, sulfo-SMCC (sulfosuccinimidyl 4-[N-maleimidomethyl]cyclohexane-1-carboxylate), amine/BMPH (N-[β-Maleimidopropionic acid]hydrazide.TFA) and sulfo-SBED sulfosuccinimidyl[2-6-(biotinamido)-2-(p-azidobenzamido)-hexanoamido]-ethyl-1,3′-dithiopropionate.

9. The multichromophore-biomolecule conjugate according to claim 8 , wherein the light harvesting multichromophore further comprises the structure:

wherein: L is a linker to a bioconjugation site A covalently linked to the sensor biomolecule; and *=site for covalent attachment to unsaturated backbone of the multichromophore.

10. A light harvesting water soluble multichromophore comprising a conjugated polymer having a backbone of π-conjugated repeat units and a bioconjugation functional group capable of covalently linking to a sensor biomolecule and that does not comprise a biotin group, wherein the multichromophore has the structure:

wherein:

CP 1 is present and is a fluorene repeat unit;

CP 2 is an aromatic repeat unit;

CP 3 is present and is an aromatic repeat unit comprising a bioconjugation functional group capable of covalently linking to a biomolecule or dye and that does not comprise a biotin group;

m is 1 to 10,0000;

n is independently 1 to 10,000 and; and

b is 0 to 250 and a and c are independently 1 to 250, wherein a+b+c>1.

11. The light harvesting water soluble multichromophore according to claim 10 , wherein the multichromophore is substituted with a plurality of charge neutral water-soluble groups.

12. The light harvesting water soluble multichromophore according to claim 11 , wherein CP 1 and CP 2 are each independently substituted with one or more water-soluble groups.

13. The light harvesting water soluble multichromophore according to claim 12 , wherein the water-soluble groups comprise one or more groups selected from ethylene glycol oligomer, ethylene glycol polymer, ω-ammonium alkoxy salt and ω-sulfonate alkoxy salt.

14. The light harvesting water soluble multichromophore according to claim 10 , wherein the bioconjugation functional group is selected from maleimide, thiol, succimidyl ester, amine, azide and carboxy/EDC (1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride).

15. An aqueous composition comprising a multichromophore-biomolecule conjugate comprising:

a sensor biomolecule covalently linked to a light harvesting multichromophore via a bioconjugation site;

wherein the light harvesting multichromophore is a conjugated polymer having a backbone of π-conjugated repeat units and comprises the structure:

wherein:

CP 1 is present and is a fluorene repeat unit;

CP 2 is an aromatic repeat unit;

CP 3 is present and is an aromatic repeat unit comprising a bioconjugation functional group capable of covalently linking to a biomolecule or dye and does not comprise a biotin group;

m is 1 to 10,0000;

n is independently 1 to 10,000 and; and

b is 0 to 250 and a and c are 1 to 250, wherein a+b+c>1.

16. The composition according to claim 15 , wherein the sensor biomolecule is a protein, an antibody, a nucleic acid, an affinity ligand, a sugar, a lipid or a peptide.

17. The multichromophore-biomolecule conjugate according to claim 16 , wherein the sensor biomolecule is a protein, an antibody or a nucleic acid.

18. The multichromophore-biomolecule conjugate according to claim 17 , wherein the sensor biomolecule is an antibody.

19. The composition according to claim 15 , wherein the bioconjugation site results from a linking chemistry selected from maleimide, thiol, succimidylester (NHS ester), amine, azide chemistry, carboxy/EDC (1-Ethyl-3-[3-dimethylaminopropyl]carbodiimide hydrochloride, sulfo-SMCC (sulfosuccinimidyl 4-[N-maleimidomethyl]cyclohexane-1-carboxylate), amine/BMPH (N-[β-Maleimidopropionic acid]hydrazide.TFA) and sulfo-SBED sulfosuccinimidyl[2-6-(biotinamido)-2-(p-azidobenzamido)-hexanoamido]-ethyl-1,3′-dithiopropionate.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2019
From: SIRIGEN, INC.
To: SIRIGEN II LIMITED
Reel/Frame 050867/0583 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 30, 2019
From: GAYLORD, BRENT S.; HONG, JANICE W.; FU, TSU-JU; SUN, CHENGJUN; BALDOCCHI, RUSSELL
To: SIRIGEN, INC.
Reel/Frame 050879/0187 →
Continuity (8)
Continuation 16154541 · Oct 8, 2018
Continuation 15799969 · Oct 31, 2017
Continuation 15162436 · May 23, 2016
Continuation 14307258 · Jun 17, 2014
Continuation 13195747 · Aug 1, 2011
Continuation 11868870 · Oct 8, 2007
Provisional Application 60828615 · Oct 6, 2006
Related Publication 20190376977A1 · Dec 12, 2019
Cited By (3)
US 12,312,437 US 12,366,577 US 12,366,578