IP Library Granted Patent US 11,208,663
Granted Patent B2
US 11,208,663 · App. 16/283,022 · Granted Dec 28, 2021

Post-selex modification methods

Inventors: Thale C. Jarvis (Boulder, CO); John C. Rohloff (Boulder, CO); Amy D. Gelinas (Lafayette, CO); Chi Zhang (Superior, CO); Daniel W. Drolet (Boulder, CO); Sheela M. Waugh (Erie, CO); Nebojsa Janjic (Boulder, CO)
Assignee: SomaLogic, Inc.
C12N15/115C12N2310/16C12N2310/315C12N2310/318C12N2310/321C12N2310/335C12N2320/30
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Quick Facts
Patent No.
US 11,208,663
App. No.
16/283,022
Granted
Dec 28, 2021
Kind
B2
Abstract

Aptamers that bind PDGF and aptamers that bind VEGF are provided. In addition, aptamer constructs comprising a PDGF aptamer and a VEGF aptamer are provided. Pharmaceutical compositions comprising the aptamers and aptamer constructs are provided, as well as methods of treating conditions using the aptamers and aptamer constructs.

Claims (11)

1. An aptamer comprising at least one first C-5 modified uridine and at least one second C-5 modified uridine, wherein the first C-5 modified uridine is selected from 5-(N-thiophenylmethylcarboxyamide)-2′-deoxyuridine (ThdU), 5-(N-4-fluorobenzylcarboxyamide)-2′-deoxyuridine (FBndU), 5-(N-phenethylcarboxyamide)-2′-deoxyuridine (PEdU), 5-(N-3-phenylpropylcarboxyamide)-2′-deoxyuridine (PPdU), 5-(N-tyrosylcarboxyamide)-2′-deoxyuridine (TyrdU), 5-(N-3,4-methylenedioxybenzylcarboxyamide)-2′-deoxyuridine (MBndU), 5-(N-2-naphthylmethylcarboxyamide)-2′-deoxyuridine (2NapdU), 5-(N-2-naphthylmethylcarboxyamide)-2′-O-methyluridine, 5-(N-2-naphthylmethylcarboxyamide)-2′-fluorouridine, 5-(N-1-naphthylethylcarboxyamide)-2′-deoxyuridine (NEdU), 5-(N-1-naphthylethylcarboxyamide)-2′-O-methyluridine, 5-(N-1-naphthylethylcarboxyamide)-2′-fluorouridine, 5-(N-2-naphthylethylcarboxyamide)-2′-deoxyuridine (2NEdU), 5-(N-2- naphthylethylcarboxyamide)-2′-O-methyluridine, 5-(N-2-naphthylethylcarboxyamide)-2′-fluorouridine, 5-(N-3-benzothiophenylethylcarboxyamide)-2′-deoxyuridine (BTdU), 5-(N-3-benzothiophenylethylcarboxyamide)-2′-O-methyluridine, and 5-(N-3-benzothiophenylethylcarboxyamide)-2′-fluorouridine;

and the second C-5 modified uridine is 5-(N-benzylcarboxyamide)-2′-deoxyuridine (BndU), 5-(N-benzylcarboxyamide)-2′-O-methyluridine, or 5-(N-benzylcarboxyamide)-2′-fluorouridine.

2. The aptamer of claim 1 , wherein the first C-5 modified uridine is selected from ThdU, FBndU, PPdU, MBndU, 2NapdU, 5-(N-2-naphthylmethylcarboxyamide)-2′-O-methyluridine, 5-(N-2-naphthylmethylcarboxyamide)-2′-fluorouridine, NEdU, 5-(N-1-naphthylethylcarboxyamide)-2′-O-methyluridine, and 5-(N-1-naphthylethylcarboxyamide)-2′-fluorouridine.

3. The aptamer of claim 1 , wherein the first C-5 modified uridine is selected from ThdU and FBndU.

4. The aptamer of claim 1 , wherein the aptamer consists of at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18, at least 19, at least 20, at least 21, at least 22, at least 23, at least 24, at least 25, at least 26, at least 27, at least 28, at least 29, or at least 30 contiguous nucleotides.

5. The aptamer of claim 4 , wherein the aptamer consists of up to about 100 nucleotides, up to about 95 nucleotides, up to about 90 nucleotides, up to about 85 nucleotides, up to about 80 nucleotides, up to about 75 nucleotides, up to about 70 nucleotides, up to about 65 nucleotides, up to about 60 nucleotides, up to about 55 nucleotides, up to about 50 nucleotides, up to about 45 nucleotides, up to about 40 nucleotides, up to about 35 nucleotides, up to about 30 nucleotides, up to about 25 nucleotides, or up to about 20 nucleotides.

6. An aptamer comprising at least one first C-5 modified uridine and at least one second C-5 modified uridine, wherein the first C-5 modified uridine is selected from a 5-(N-4-fluorobenzylcarboxyamide)-2′-deoxyuridine (FBndU), 5-(N-2-naphthylmethylcarboxyamide)-2′-deoxyuridine (2NapdU), 5-(N-2-naphthylmethylcarboxyamide)-2′-O-methyluridine, 5-(N-2-naphthylmethylcarboxyamide)-2′-fluorouridine, 5-(N-phenethylcarboxyamide)-2′-deoxyuridine (PEdU), 5-(N-tyrosylcarboxyamide)-2′-deoxyuridine (TyrdU), 5-(N-1-naphthylethylcarboxyamide)-2′-deoxyuridine (NEdU), 5-(N-1-naphthylethylcarboxyamide)-2′-O-methyluridine, 5-(N-1-naphthylethylcarboxyamide)-2′-fluorouridine, 5-(N-2-naphthylethylcarboxyamide)-2′-deoxyuridine (2NEdU), 5-(N-2-naphthylethylcarboxyamide)-2′-O-methyluridine, 5-(N-2-naphthylethylcarboxyamide)-2′-fluorouridine, 5-(N-3,4-methylenedioxybenzylcarboxyamide)-2′-deoxyuridine (MBndU), 5-(N-3-phenylpropylcarboxyamide)-2′-deoxyuridine (PPdU), 5-(N-thiophenylmethylcarboxyamide)-2′-deoxyuridine (ThdU), 5-(N-3-benzothiophenylethylcarboxyamide)-2′-deoxyuridine (BTdU), 5-(N-3-benzothiophenylethylcarboxyamide)-2′-O-methyluridine, and 5-(N-3-benzothiophenylethylcarboxyamide)-2′-fluorouridine;

and the second C-5 modified uridine is 5-(N-naphthylmethylcarboxyamide)-2′-deoxyuridine (NapdU), 5-(N-naphthylmethylcarboxyamide)-2′-O-methyluridine, or 5-(N-naphthylmethylcarboxyamide)-2′-fluorouridine.

7. The aptamer of claim 6 , wherein the first C-5 modified uridine is selected from FBndU, NEdU, 5-(N-1-naphthylethylcarboxyamide)-2′-O-methyluridine, 5-(N-1-naphthylethylcarboxyamide)-2′-fluorouridine, MBndU, BTdU, 5-(N-3-benzothiophenylethylcarboxyamide)-2′-O-methyluridine, and 5-(N-3-benzothiophenylethylcarboxyamide)-2′-fluorouridine.

8. The aptamer of claim 6 , wherein the aptamer consists of at least 12, at least 13, at least 14, at least 15, at least 16, at least 17, at least 18, at least 19, at least 20, at least 21, at least 22, at least 23, at least 24, at least 25, at least 26, at least 27, at least 28, at least 29, or at least 30 contiguous nucleotides.

9. The aptamer of claim 8 , wherein the aptamer consists of up to about 100 nucleotides, up to about 95 nucleotides, up to about 90 nucleotides, up to about 85 nucleotides, up to about 80 nucleotides, up to about 75 nucleotides, up to about 70 nucleotides, up to about 65 nucleotides, up to about 60 nucleotides, up to about 55 nucleotides, up to about 50 nucleotides, up to about 45 nucleotides, up to about 40 nucleotides, up to about 35 nucleotides, up to about 30 nucleotides, up to about 25 nucleotides, or up to about 20 nucleotides.

Assignments (2)
MERGER AND CHANGE OF NAME Recorded Jan 14, 2022
From: SOMALOGIC, INC.; SOMALOGIC OPERATING CO., INC.
To: SOMALOGIC OPERATING CO., INC.
Reel/Frame 058736/0574 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 26, 2019
From: JARVIS, THALE C.; ROHLOFF, JOHN C.; GELINAS, AMY D.; ZHANG, CHI; DROLET, DANIEL W.; WAUGH, SHEELA M.; JANJIC, NEBOJSA
To: SOMALOGIC, INC.
Reel/Frame 049592/0913 →
Continuity (8)
Continuation 15602377 · May 23, 2017
Continuation 15189159 · Jun 22, 2016
Division 14381679
Provisional Application 61616881 · Mar 28, 2012
Provisional Application 61648394 · May 17, 2012
Provisional Application 61719354 · Oct 26, 2012
Provisional Application 61722099 · Nov 2, 2012
Related Publication 20200056181A1 · Feb 20, 2020