IP Library › Granted Patent US 11,884,826
Granted Patent B2
US 11,884,826 · App. 17/556,800 · Granted Jan 30, 2024

Protected dye-labeled reagents

Inventors: Lubomir Sebo (Redwood City, CA); Honey Osuna (San Francisco, CA); Stephen Yue (Eugene, OR); Yuri Lapin (Newark, CA)
Assignee: Pacific Biosciences of California, Inc.
C09B69/105C07D495/04C07H19/10C07H19/207C12Q1/6869G01N21/6428G01N2021/6439
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Quick Facts
Patent No.
US 11,884,826
App. No.
17/556,800
Granted
Jan 30, 2024
Kind
B2
Abstract

Labeled nucleotide analogs comprising at least one avidin protein, at least one dye-labeled compound, and at least one nucleotide compound are provided. The analogs are useful in various fluorescence-based analytical methods, including the analysis of highly multiplexed optical reactions in large numbers at high densities, such as single molecule real time nucleic acid sequencing reactions. The analogs are detectable with high sensitivity at desirable wavelengths. They contain structural components that modulate the interactions of the analogs with DNA polymerase, thus decreasing photodamage and improving the kinetic and other properties of the analogs in sequencing reactions. Also provided are nucleotide and dye-labeled compounds of the subject analogs, as well as intermediates useful in the preparation of the compounds and analogs. Compositions comprising the compounds, methods of synthesis of the intermediates, compounds, and analogs, and mutant DNA polymerases are also provided.

Claims (44)

1. A dye-labeled compound of structural formula (IIIG):

wherein

each L′ is independently a dye compound linker element;

each S is independently a shield element, wherein the shield element does not comprise a protein;

each Dye is independently either an acceptor dye or a donor dye;

each B″ is independently a terminal coupling element;

each p is independently 0 or 1; and

each r″ is independently an integer from 0 to 8;

s is an integer from 1 to 6; and

t is 0 or 1;

wherein the compound comprises at least one shield element, at least one acceptor dye, and at least one donor dye; and

wherein the terminal coupling element comprises a first reactive functional group or a residue derived from a first reactive functional group.

2. The dye-labeled compound of claim 1 , wherein each r″ is independently an integer from 0 to 4.

3. The dye-labeled compound of claim 1 , wherein s is an integer from 1 to 4.

4. The dye-labeled compound of claim 1 comprising at least two donor dyes.

5. The dye-labeled compound of claim 4 , wherein each donor dye is directly coupled to a donor shield element.

6. The dye-labeled compound of claim 1 comprising at least two acceptor dyes.

7. The dye-labeled compound of claim 6 , wherein each acceptor dye is directly coupled to an acceptor shield element.

8. The dye-labeled compound of claim 1 comprising at least four donor dyes and at least two acceptor dyes.

9. The dye-labeled compound of claim 1 , comprising at least two shield elements.

10. The dye-labeled compound of claim 1 , wherein at least one dye compound linker element comprises a shield element or a side chain element.

11. The dye-labeled compound of claim 1 , wherein the at least one shield element comprises a plurality of side chains.

12. The dye-labeled compound of claim 11 , wherein at least one side chain has a molecular weight of at least 300.

13. The dye-labeled compound of claim 11 , wherein all of the side chains have a molecular weight of at least 300.

14. The dye-labeled compound of claim 11 , wherein at least one side chain comprises a polyethylene glycol.

15. The dye-labeled compound of claim 11 , wherein at least one side chain comprises a negatively-charged component.

16. The dye-labeled compound of claim 15 , wherein the negatively-charged component comprises a sulfonic acid.

17. The dye-labeled compound of claim 11 , wherein at least one side chain comprises a substituted phenyl group.

18. The dye-labeled compound of claim 17 , wherein the at least one side chain comprises the structure:

wherein each x is independently an integer from 1 to 6.

19. The dye-labeled compound of claim 18 , wherein each x is independently an integer from 1 to 4.

20. The dye-labeled compound of claim 11 , wherein at least one side chain comprises a triazole.

21. The dye-labeled compound of claim 11 , wherein at least one side chain comprises the structure:

22. The dye-labeled compound of claim 1 , wherein the at least one shield element comprises the structure:

wherein each y is independently an integer from 1 to 6.

23. The dye-labeled compound of claim 1 , wherein the at least one shield element comprises the structure:

24. The dye-labeled compound of claim 1 , wherein t is 1.

25. The dye-labeled compound of claim 1 , wherein the at least one acceptor dye or the at least one donor dye is a cyanine dye.

26. The dye-labeled compound of claim 1 , wherein the compound does not contain a nucleoside.

27. The dye-labeled compound of claim 1 , wherein the terminal coupling element comprises a first reactive functional group.

28. The dye-labeled compound of claim 1 , wherein the terminal coupling element comprises a residue derived from a first reactive functional group.

29. The dye-labeled compound of claim 28 , wherein the residue derived from the first reactive functional group is an amide moiety.

30. The dye-labeled compound of claim 28 , wherein the residue derived from the first reactive functional group results from a click reaction.

31. The dye-labeled compound of claim 1 , wherein the terminal coupling element is connected by the residue derived from the first reactive functional group to a nucleotide compound.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2024
From: SEBO, LUBOMIR; OSUNA, HONEY; YUE, STEPHEN; LAPIN, YURI
To: PACIFIC BIOSCIENCES OF CALIFORNIA, INC.
Reel/Frame 066070/0311 →
Continuity (4)
Continuation 16779439 · Jan 31, 2020
Continuation 15357965 · Nov 21, 2016
Provisional Application 62258415 · Nov 20, 2015
Related Publication 20220396702A1 · Dec 15, 2022
Cited By (1)
US 12,391,834