IP Library › Granted Patent US 10,641,777
Granted Patent B2
US 10,641,777 · App. 15/799,969 · Granted May 5, 2020

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: SIRIGEN, INC.
G01N33/582C08G61/02C08G61/12G01N33/542C08G2261/3142C08G2261/3221C08G2261/3241C08G2261/3246C08G2261/522C08G2261/78C08G2261/94H01L51/0039Y10T436/13
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Quick Facts
Patent No.
US 10,641,777
App. No.
15/799,969
Granted
May 5, 2020
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 (30)

1. A multichromophore-biomolecule conjugate comprising:

a sensor biomolecule covalently linked to a π-conjugated repeat unit of a light harvesting multichromophore through a linker via a bioconjugation site, wherein the linker and the bioconjugation site do not comprise a biotin group, wherein the sensor biomolecule is a protein, an antibody, a nucleic acid, a sugar, a lipid or a peptide;

wherein the light harvesting multichromophore is a conjugated polymer having a backbone of π-conjugated repeat units comprising a fluorene unit of the structure:

wherein:

each R 1 is a water solubilizing group; and

* is a site for covalent attachment of the fluorene unit to another group of the backbone.

2. The multichromophore-biomolecule conjugate according to claim 1 , wherein the sensor biomolecule is a protein, an antibody, a nucleic acid, or a peptide.

3. The multichromophore-biomolecule conjugate according to claim 2 , wherein the sensor biomolecule is a protein, an antibody or a nucleic acid.

4. The multichromophore-biomolecule conjugate according to claim 3 , wherein the sensor biomolecule is an antibody.

5. The multichromophore-biomolecule conjugate according to claim 1 , wherein the π-conjugated repeat units further comprise an aromatic repeat unit.

6. The multichromophore-biomolecule conjugate according to claim 5 , wherein the aromatic repeat unit is selected from benzene, naphthalene, anthracene, fluorene, thiophene, furan, pyridine, and oxadiazole, each optionally substituted.

7. The multichromophore-biomolecule conjugate according to claim 6 , wherein the aromatic repeat unit is a benzene covalently attached with a para configuration to the backbone of the conjugated polymer.

8. The multichromophore-biomolecule conjugate according to claim 6 , wherein the aromatic repeat unit is an oxadiazole.

9. The multichromophore-biomolecule conjugate according to claim 1 , wherein the conjugated polymer is a charge-neutral conjugated polymer.

10. The multichromophore-biomolecule conjugate according to claim 1 , wherein each R 1 is independently selected from the group consisting of ethylene glycol oligomers, ethylene glycol polymers, ω-ammonium alkoxy salts and ω-sulfonate alkoxy salts.

11. The multichromophore-biomolecule conjugate according to claim 1 , further comprising a linker unit comprising a second bioconjugation site.

12. The multichromophore-biomolecule conjugate according to claim 1 , wherein the bioconjugation site comprises 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), and amine/BMPH (N-[β-Maleimidopropionic acid]hydrazide.TFA).

13. The multichromophore-biomolecule conjugate according to claim 11 , further comprising a signaling chromophore covalently linked to the light harvesting multichromophore via the second bioconjugation site, wherein the signaling chromophore is capable of receiving energy from the multichromophore upon excitation of the light harvesting multichromophore.

14. A multichromophore-biomolecule conjugate comprising:

a sensor biomolecule covalently linked to a π-conjugated repeat unit of a light harvesting multichromophore through a linker via a bioconjugation site, wherein the linker and the bioconjugation site do not comprise a biotin group, wherein the sensor biomolecule is a protein, an antibody or a nucleic acid;

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

a fluorene unit of the structure:

wherein each R 1 is a water solubilizing group; and * is a site for covalent attachment of the fluorene unit to another group of the backbone; and

an aromatic repeat unit selected from an oxadiazole and a benzene covalently attached with a para configuration to other groups of the backbone.

15. The multichromophore-biomolecule conjugate according to claim 14 , wherein the sensor biomolecule is a nucleic acid.

16. The multichromophore-biomolecule conjugate according to claim 14 , wherein the sensor biomolecule is an antibody.

17. The multichromophore-biomolecule conjugate according to claim 14 , wherein the conjugated polymer is a charge-neutral conjugated polymer.

18. The multichromophore-biomolecule conjugate according to claim 14 , wherein each R 1 is independently selected from the group consisting of ethylene glycol oligomers, ethylene glycol polymers, ω-ammonium alkoxy salts and ω-sulfonate alkoxy salts.

19. The multichromophore-biomolecule conjugate according to claim 14 , wherein the bioconjugation site comprises 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), and amine/BMPH (N-[β-Maleimidopropionic acid]hydrazide.TFA).

20. The multichromophore-biomolecule conjugate according to claim 14 , further comprising a signaling chromophore covalently linked to the light harvesting multichromophore via a second bioconjugation site, wherein the signaling chromophore is capable of receiving energy from the multichromophore upon excitation of the light harvesting multichromophore.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 12, 2018
From: GAYLORD, BRENT S.; HONG, JANICE W.; FU, TSU-JU; SUN, CHENGJUN; BALDOCCHI, RUSSELL
To: SIRIGEN, INC.
Reel/Frame 044608/0026 →
Continuity (6)
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 20180059117A1 · Mar 1, 2018
Cited By (7)
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