IP Library Granted Patent US 12,428,666
Granted Patent B2
US 12,428,666 · App. 17/250,023 · Granted Sep 30, 2025

Compositions and methods related to kethoxal derivatives

Inventors: Chuan He (Chicago, IL); Xiaocheng Weng (Chicago, IL); Tong Wu (Chicago, IL)
Assignee: THE UNIVERSITY OF CHICAGO
C12Q1/6806C07C69/003C12N15/11C12N2830/46C12Q2565/518
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,428,666
App. No.
17/250,023
Granted
Sep 30, 2025
Kind
B2
Abstract

Embodiments are directed to N 3 -kethoxal reagents and derivatives thereof, and related methods that allow fast and reversible labeling of single-stranded nucleic acids in live cells. By way of example, one aspect is directed to a process for reversible labeling of single-stranded guanine bases in live cells, which results in an effective in vivo method for transcriptome-wide RNA secondary structure mapping and RNA G-quadruplex prediction.

Claims (22)

1. A compound of the formula:

wherein Y is an alkyne, an azide, a strained alkyne, a diene, a dieneophile, an alkoxyamine, a phosphine, a hydrazide, a thiol, or an alkene; and

X is a C1 to C10 alkyl or a C4 to C10 polyethylene glycol linker.

2. The compound of claim 1 , wherein Y is an azide.

3. A compound of the formula:

wherein Y is an alkyne, an azide, a strained alkyne, a diene, a dieneophile, an alkoxyamine, a phosphine, a hydrazide, a thiol, or an alkene; and X is CH 2 .

4. The compound of claim 1 , wherein the compound is of formula:

5. A method for labeling a guanine base comprising contacting a guanine base to be labeled with a compound of claim 1 to form a reaction mixture and incubating the reaction mixture at 30 to 40° C. for at least 5 minutes.

6. The method of claim 5 , wherein the compound is N3-kethoxal.

7. The method of claim 5 , wherein the guanine base is comprised in a polynucleotide.

8. The method of claim 5 , wherein the polynucleotide is a ribonucleic acid (RNA).

9. The method of claim 5 , wherein the polynucleotide is a deoxyribonucleic acid (DNA).

10. A method for labeling a single stranded nucleic acid in a cell comprising

(i) contacting a target cell with a compound of claim 1 , wherein Y is an azide, to form a treated cell comprising a nucleic acid having kethoxal derivative-labeled guanine bases;

(ii) contacting the treated cell with a crosslinking moiety comprising at least two click chemistry reactive moieties and a tag, wherein the crosslinking moiety crosslinks two proximal kethoxal derivative-labeled guanines to form a crosslinked nucleic acid; and

(iii) fragmenting and isolating the crosslinked nucleic acid using a reagent with an affinity for the tag;

wherein the click chemistry reactive moieties are alkyne moieties.

11. The method of claim 10 , wherein the tag is biotin, and wherein the reagent with an affinity for the tag is streptavidin.

12. The method of claim 10 , wherein the click chemistry reactive moieties are dibenzocyclooctyne moieties.

13. The method of claim 10 , wherein the crosslinked nucleic acid is RNA.

14. A compound having the formula:

15. A composition comprising the compound of claim 14 .

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 6, 2020
From: HE, CHUAN; WU, TONG; WENG, XIAOCHENG
To: THE UNIVERSITY OF CHICAGO
Reel/Frame 054292/0958 →
Continuity (3)
Provisional Application 62668543 · May 8, 2018
Provisional Application 62668994 · May 9, 2018
Related Publication 20210214773A1 · Jul 15, 2021
References Cited (46)
US 2889243A · Underwood et al. · 1959 [cited by applicant]
US 5385933A · Rabinovitz et al. · 1995 [cited by applicant]
US 7133783B2 · Noller et al. · 2006 [cited by applicant]
CN 112384524A · 2021 [cited by applicant]
JP H02150299 · 1990 [cited by applicant]
WO WO2019217549A1 · 2019 [cited by applicant]
Aw et al, “In Vivo Mapping of Eukaryotic RNA Interactomes Reveals Principles of Higher-Order Organiation and Regulation”, Mol Cell., 62(4):603-617, 2016. [cited by applicant]
Buenrostro et al., “Transposition of native chromatin for fast and sensitive epigenomic profiling of open chromatin, DNA-binding proteins and nucleosome position”, Nat Methods., 10(12):1213-1218, 2013. [cited by applicant]
Core et al., “Nascent RNA sequencing reveals widespread pausing and divergent initiation at human promoters”, 322(5909):1845-1848, 2008. [cited by applicant]
Ding et al., “In vivo genome-wide profiling of RNA secondary structure reveals novel regulatory features”, Nature., 505(7485):696-700, 2014. [cited by applicant]
Esfand and Tomalia, “Poly(amidoamine) (PAMAM) dendrimers: from biomimicry to drug delivery and biomedical applications”, Drug Discov Today., 6(8):427-436, 2001. [cited by applicant]
Feng et al., “Light-activated chemical probing of nucleobase solvent accessibility inside cells”, Nat Chem Biol., 14(3):276-283, 2018. [cited by applicant]
Jiang et al., “Enantioselective synthesis for the antipodes of slagenins B and C: establishment of absolute stereochemistry”, Org Lett., 3(25):4011-4013, 2001. [cited by applicant]
Kertesz et al., “Genome-wide measurement of RNA secondary structure in yeast”, Nature, 467(7311):103-107, 2010. [cited by applicant]
Kubota et al., “Progress and challenges for chemical probing of RNA structure inside living cells”, Nat Chem Biol., 11(12):933-941, 2015. [cited by applicant]
Lee et al., “Comparison of SHAPE reagents for mapping RNA structures inside living cells”, RNA, 23:169-174, 2017. [cited by applicant]
Lewis et al., “RNA modifications and structures cooperate to guide RNA-protein interactions”, Nat Rev Mol Cell Biol., 18(3):202-210, 2017. [cited by applicant]
Lo et al., “Synthesis, radiochemical characterization and biodistribution of Tc-99m labeled kethoxal bis(thiosemicarbazone) complexes”, Journal of Labelled Compounds and Radiopharmaceuticals, 44:S654-S656, 2001. [cited by applicant]
Lu and Chang, “Decoding the RNA structurome”, Curr Opin Struct Biol., 36:142-148, 2016. [cited by applicant]
Lu et al., “RNA Duplex Map in Living Cells Reveals Higher-Order Transcriptome Structure”, Cell., 165(5):1267-1279, 2016. [cited by applicant]
Lucks et al., “Multiplexed RNA structure characterization with selective 2′-hydroxyl acylation analyzed by primer extension sequencing (SHAPE-Seq)”, Proc Natl. Acad Sci USA., 108(27):11063-11068, 2011. [cited by applicant]
Nainar et al., “Temporal Labeling of Nascent RNA Using Photoclick Chemistry in Live Cells”, J Am Chem Soc., 139(24):8090-8093, 2017. [cited by applicant]
Pubmed Compound Summary for CID 109466, Butanal, 3-(heptyloxy)-2-oxo-, U.S. National Library Medicine, Aug. 8, 2005 (Aug. 8, 2005), p. 1-10; p. 2 (https://pubchem.ncbi.nlm.nih.gov/compound/109466). [cited by applicant]
Pubmed Compound Summary for CID 134685, “Bikethoxal”, U.S. National Library of Medicine, Aug. 8, 2005 (Aug. 8, 2005), p. 1-10; p. 2 (https://pubchem.ncbi.nlm.nih.gov/compound/134685). [cited by applicant]
Pubmed Compound Summary for CID 226599, ‘3-[2-(Methoxymethoxy)ethoxy]-2-oxobutanal’, U.S. National Library of Medicine, Mar. 26, 2005 (Mar. 26, 2005), p. 1-8; p. 2 (https://pubchem.ncbi.nlm.nih.gov/compound/226599). [cited by applicant]
Ramani et al., “High-throughput determination of RNA structure by proxmity ligation”, Nat Biotechnol., 33(9):980-984, 2015. [cited by applicant]
Rouskin et al., “Genome-wide probing of RNA structure reveals active unfolding of mRNA structures in vivo”, Nature., 505(7485):701-705, 2014. [cited by applicant]
Sharma et al, “Global Mapping of Human RNA-RNA Interactions”, Mol Cell., 62(4):618-626, 2016. [cited by applicant]
Siegfried et al., “RNA motif discovery by SHAPE and mutational profiling (SHAPE-MaP)”, Nat. Methods, 11(9):959-965, 2014. [cited by applicant]
Spitale et al., “Structural imprints in vivo decode RNA regulatory mechanisms”, Nature., 519(7544):486-490, 2015. [cited by applicant]
Strobel et al., “High-throughput determination of RNA structures”, Nat Rev Genet., 19(10):615-634, 2018. [cited by applicant]
Talkish et al, “Mod-seq: high-throughput sequencing for chemical probing of RNA structure”, RNA, 20(5):713-720, 2014. [cited by applicant]
Underwood et al., “FragSeq: transcriptome-wide RNA structure probing using high-througput sequencing”, Nat Methods., 7(12):995-1001, 2010. [cited by applicant]
Wan et al., “Landscape and variation of RNA secondary structure across the human transcriptome”, Nature., 505(7485):706-709, 2014. [cited by applicant]
Xu and Culver, “Chemical probing of RNA and RNA/protein complexes”, Methods Enzymol., 468:147-165, 2009. [cited by applicant]
Zubradt et al., “DMS-MaPseq for genome-wide or targeted RNA structure probing in vivo”, Nat. Methods., 14(1):75-82, 2017. [cited by applicant]
Shapiro, et al: “On the Reaction of Guanine with Glyoxal, Pyruvaldehyde, and Kethoxal, and the Structure of the Acylguanines. A New Synthesis of N [cited by applicant]
“3-Azido-2-oxopropanal” Pubchem CID 54201527 deposited on Dec. 4, 2011, pp. 1-8, https://pubchem.ncbi.nlm.nih.gov/compound/3-Azido-2-oxopropanal. Accessed Sep. 20, 2024. [cited by applicant]
Bocchetta et al., “23S rRNA Positions Essential for tRNA binding in Ribosomal Functional Sites,” Proc. Natl. Acad. Sci. USA, 1998, vol. 95, pp. 3525-3530. [cited by applicant]
Booth and Sartorelli, “Synergistic Interaction of Kethoxal bis(Thiosemicarbazone) and Cupric Ions in Sarcoma 180,” Nature 1966, 210, 104-105. [cited by applicant]
Brewer et al., “Ribonucleic acid-protein crosslinking within the intact [cited by applicant]
Christian et al., “Analysis of substrate recognition by the ribonucleoprotein endonuclease RNase P,” Methods, 2002, vol. 28, pp. 307-322. [cited by applicant]
International Search Report and Written Opinion issued in PCT Application No. PCT/US2020/070073, dated Sep. 14, 2020, 10 pages. [cited by applicant]
Noller et al., “Functional Modification of 16S Ribosomal RNA by Kethoxal,” Proc. Natl. Acad. Sci. USA, 1972, vol. 69(11 ), pp. 3115-3118. [cited by applicant]
Staehelin, M. “Inactivation of virus nucleic acid with glyoxal derivatives,” Biochimca Biophysica Acta 1959, 31 :448-54. [cited by applicant]
Tiffany et al., “Antiviral Compounds. I. Aliphatic Glyoxals, a-Hydroxyaldehydes and Related Compounds,” J. Am. Chem. Soc. 1957, 79(7), 1682-1687. [cited by applicant]