Linkers and methods for optical detection and sequencing

Patent metadata

Field	Value
Publication number	US-11946097-B2
Application number	US-202217697636-A
Country	US
Kind code	B2
Filing date	Mar 17, 2022
Priority date	Feb 19, 2019
Publication date	Apr 2, 2024
Grant date	Apr 2, 2024

Abstract

The present disclosure provides labeling reagents for labeling substrates such as nucleotides, proteins, antibodies, lipids, and cells. The labeling reagents provided herein may comprise fluorescent labels and semi-rigid linkers. Methods for nucleic acid sequencing using materials comprising such labeling reagents are also provided here.

First claim

What is claimed is:

1. A kit comprising: a plurality of linkers, wherein a linker of said plurality of linkers comprises (i) one or more water soluble groups and (ii) two or more ring systems, wherein said linker is coupled to a nucleotide via a nucleobase of said nucleotide, wherein at least two ring systems of said two or more ring systems are connected to each other by no more than two atoms, and wherein said linker comprises a non-proteinogenic amino acid comprising a ring system of said two or more ring systems.

2. The kit of claim 1 , wherein said linker is coupled to a plurality of substrates.

3. The kit of claim 2 , wherein said plurality of substrates is selected from the group consisting of a nucleotide, a protein, a lipid, a cell, and an antibody.

4. The kit of claim 1 , wherein said linker is connected to a fluorescent dye.

5. The kit of claim 1 , wherein said linker comprises a plurality of non-proteinogenic amino acids.

6. The kit of claim 5 , wherein said linker comprises a plurality of hydroxyprolines.

7. The kit of claim 6 , wherein said linker comprises at least three hydroxyprolines.

8. The kit of claim 7 , wherein said linker comprises at least ten hydroxyprolines.

9. The kit of claim 1 , wherein said at least two ring systems of said two or more ring systems are connected to each other by an sp 2 carbon atom.

10. The kit of claim 1 , wherein said at least two ring systems of said two or more ring systems are connected to each other directly without an intervening atom.

11. The kit of claim 1 , wherein said one or more water soluble groups are selected from the group consisting of a pyridinium, an imidazolium, a quaternary ammonium group, a sulfonate, a phosphate, an alcohol, an amine, an imine, a nitrile, an amide, a thiol, a carboxylic acid, a polyether, an aldehyde, a boronic acid, and a boronic ester.

12. The kit of claim 1 , wherein said linker further comprises a cleavable group that is configured to be cleaved to separate a first portion of said linker from a second portion of said linker.

13. The kit of claim 12 , wherein said cleavable group is selected from the group consisting of an azidomethyl group, a disulfide bond, a hydrocarbyldithiomethyl group, and a 2-nitrobenzyloxy group.

14. The kit of claim 1 , wherein said linker comprises a moiety selected from the group consisting of

15. The kit of claim 1 , wherein said plurality of linkers comprises a first linker associated with a first substrate and a second linker associated with a second substrate, wherein said first substrate and said second substrate are different types of substrates.

16. The kit of claim 15 , wherein said first linker and said second linker comprise a same chemical structure.

17. The kit of claim 15 , wherein said first substrate and said second substrate are nucleotides comprising nucleobases of different types.

18. The kit of claim 15 , wherein said plurality of linkers further comprises a third linker associated with a third substrate and a fourth linker associated with a fourth substrate, and wherein said first substrate, said second substrate, said third substrate, and said fourth substrate are different types of substrates.

19. The kit of claim 18 , wherein said first substrate, said second substrate, said third substrate, and said fourth substrate are nucleotides comprising nucleobases of different types.

20. The kit of claim 18 , wherein said first linker and said second linker comprise a same chemical structure, and wherein said first linker and said third linker comprise different chemical structures.

Assignees

• Ultima Genomics Inc

Inventors

• Lee Linda G
• Almogy Gilad
• Menchen Steven

Classifications

• C12Q1/6823 Primary

  Release of bound markers · CPC title

• C12Q1/6869

  Methods for sequencing · CPC title

• C12Q1/6876

  Nucleic acid products used in the analysis of nucleic acids, e.g. primers or probes · CPC title

• G01N33/582 Primary

  with fluorescent label · CPC title

• C12Q1/6806 Primary

  Preparing nucleic acids for analysis, e.g. for polymerase chain reaction [PCR] assay (C12Q1/6804 takes precedence) · CPC title