IP Library Granted Patent US 12,699,094
Granted Patent B2
US 12,699,094 · App. 18/448,632 · Granted Aug 4, 2026

Fluorescent biosensor for acetyl coenzyme A

Inventors: Katharine L. Diehl (Salt Lake City, UT); Joseph J. Smith (Salt Lake City, UT)
Assignee: UNIVERSITY OF UTAH RESEARCH FOUNDATION
G01N33/5735C07K14/001C07K2319/60
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 12,699,094
App. No.
18/448,632
Filed
Aug 11, 2023
Granted
Aug 4, 2026
Kind
B2
Art Unit
1645
USPC
435/7.4
Abstract

Disclosed herein are a polypeptide biosensor and compositions comprising the polypeptide biosensor that detects acetyl coenzyme A (acetyl-CoA). The polypeptide comprises an acetyl-CoA binding protein and a fluorescent protein. Further described herein are methods of using the biosensor to detect acetyl-CoA and expression vectors comprising the biosensor.

Claims (76)

1 . A recombinant acetyl-coenzyme A (acetyl-CoA) biosensor polypeptide comprising:

an acetyl-CoA binding protein having an amino acid sequence at least 95% identical to SEQ ID NO: 1, wherein the acetyl-CoA binding protein is divided into:

a first acetyl-CoA binding protein fragment comprising an N-terminal portion of the acetyl-CoA binding protein; and

a second acetyl-CoA binding protein fragment comprising a C-terminal portion of the acetyl-CoA binding protein;

wherein the first and second acetyl-CoA binding protein fragments collectively include all of the amino acids of the acetyl-CoA binding protein; and

a fluorescent protein inserted between the first and second acetyl-CoA binding protein fragments and attached to a C-terminus of the first acetyl-CoA binding protein fragment and an N-terminus of the second acetyl-CoA binding protein fragment; and

wherein:

(i) the C-terminus is an arginine at position 69 of SEQ ID NO: 1 (Arg69) and the N-terminus is a glutamic acid at position 70 of SEQ ID NO: 1 (Glu70);

(ii) the C-terminus is a tryptophan at position 23 of SEQ ID NO: 1 (Trp23) and the N-terminus is a proline at position 24 of SEQ ID NO: 1 (Pro24);

(iii) the C-terminus is a valine at position 71 of SEQ ID NO: 1 (Val71) and the N-terminus is a threonine at position 72 of SEQ ID NO: 1 (Thr72);

(iv) the C-terminus is an aspartic acid at position 99 of SEQ ID NO: 1 (Asp99) and the N-terminus is an alanine at position 100 of SEQ ID NO: 1 (Ala100);

(v) the C-terminus is an aspartic acid at 104 of SEQ ID NO: 1 (Asp104) and the N-terminus is an arginine at position 105 of SEQ ID NO: 1 (Arg105); or

(vi) the C-terminus is a glycine at position 116 of SEQ ID NO: 1 (Gly116) and the N-terminus is a phenylalanine at position 117 of SEQ ID NO: 1 (Phe117); and

wherein the recombinant acetyl-CoA biosensor polypeptide selectively binds acetyl-CoA, and the binding of acetyl-CoA induces a change in the fluorescence of the fluorescent protein.

2 . The recombinant acetyl-CoA biosensor polypeptide of claim 1 , wherein the fluorescent protein is a circularly permuted GFP (cpGFP), a circularly permuted yellow fluorescent protein (cpYFP), or a circularly permuted blue fluorescent protein (cpBFP).

3 . The recombinant acetyl-CoA biosensor polypeptide of claim 2 , wherein the cpGFP comprises an amino acid sequence of SEQ ID NO: 2, the cpYFP comprises an amino acid sequence of SEQ ID NO: 3, and the cpBFP comprises an amino acid sequence of SEQ ID NO: 4.

4 . The recombinant acetyl-CoA biosensor polypeptide of claim 1 , wherein the acetyl-CoA binding protein comprises an amino acid sequence at least 99% identical to SEQ ID NO: 1.

5 . The recombinant acetyl-CoA biosensor polypeptide of claim 1 , wherein the acetyl-CoA binding protein comprises the amino acid sequence of SEQ ID NO: 1.

6 . The recombinant acetyl-CoA biosensor polypeptide of claim 1 , wherein:

the fluorescent protein is either directly attached to the C-terminus of the first acetyl-CoA binding protein fragment or is attached by a first amino acid linker that is from 1 to 3 amino acids in length; and

the fluorescent protein is either directly attached to the N-terminus of the second acetyl-CoA binding protein fragment or is attached by a second linker that is from 1 to 3 amino acids in length.

7 . The recombinant acetyl-CoA biosensor polypeptide of claim 6 , wherein the first and second amino acid linkers are each independently selected from the group consisting of a Gly, Gly-Ala, Ala-Ser, and Gly-Ala-Ser.

8 . The recombinant acetyl-CoA biosensor polypeptide of claim 6 , wherein:

(i) the first linker is Gly-Ala and the second linker is Gly-Ala;

(ii) the first linker is Ala-Ser and the second linker is Ala-Ser;

(iii) the first linker is Gly-Ala-Ser and the second linker is Gly;

(iv) the C-terminus and N-terminus are directly attached to the fluorescent protein;

(v) the C-terminus is directly attached to the fluorescent protein and the second linker is Gly-Ala-Ser;

(vi) the first linker is Gly-Ala-Ser and the N-terminus is directly attached to the fluorescent protein;

(vii) the first linker is Gly-Ala and the N-terminus is directly attached to the fluorescent protein; or

(viii) the first linker is Gly and the second linker is Gly-Ala-Ser.

9 . The recombinant acetyl-CoA biosensor polypeptide of claim 1 , further comprising one or more of a histidine tag, a TEV cleavage site, a tag having the amino acid sequence of SEQ ID NO: 89, a human influenza hemagglutinin (HA) tag, a nuclear export signal, a nuclear localization signal, a cytoplasmic localization signal, and a mitochondrial localization signal at the N-terminal portion of the acetyl-CoA binding protein.

10 . The recombinant acetyl-CoA biosensor polypeptide of claim 1 , wherein:

(i) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 5;

(ii) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 6;

(iii) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 7;

(iv) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 8;

(v) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 9;

(vi) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 10;

(vii) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 11;

(viii) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 12;

(ix) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 13;

(x) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 14;

(xi) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 15;

(xii) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 16;

(xiii) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 17;

(xiv) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 18; or

(xv) the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid sequence of SEQ ID NO: 19.

11 . The recombinant acetyl-CoA biosensor polypeptide of claim 10 , wherein the recombinant acetyl-CoA biosensor polypeptide comprises the amino acid of SEQ ID NO: 5.

12 . An expression vector comprising:

a nucleic acid that encodes the recombinant acetyl-CoA biosensor polypeptide of claim 1 ; and

a promoter operably linked to the nucleic acid.

13 . The expression vector of claim 12 , wherein the expression vector is a lentiviral vector, an adeno-associated virus (AAV) vector, or a cytomegalovirus (CMV) vector.

14 . A method of detecting acetyl-CoA in a sample comprising:

contacting the sample with the recombinant acetyl-CoA biosensor polypeptide of claim 1 ;

exciting the recombinant acetyl-CoA biosensor polypeptide in the sample at an excitation wavelength;

measuring a fluorescence intensity of the recombinant acetyl-CoA biosensor polypeptide in the sample at an emission wavelength; and

comparing the fluorescence intensity to a standard curve, wherein the fluorescence intensity correlates with a concentration of acetyl-CoA in the sample.

15 . The method of claim 14 , wherein the excitation wavelength is from about 460 nm to about 490 nm.

16 . The method of claim 14 , wherein the excitation wavelength is 485 nm.

17 . The method of claim 14 , wherein the emission wavelength is from about 513 nm to about 540 nm.

18 . The method of claim 14 , wherein the emission wavelength is 514 nm.

19 . The method of claim 14 , wherein the pH of the sample is maintained at a pH of 6.5-8.0.

20 . A method of monitoring acetyl-CoA activity in a cell, comprising:

providing a cell with the recombinant acetyl-CoA biosensor polypeptide of claim 1 ;

exciting the recombinant acetyl-CoA biosensor polypeptide in the cell at a first excitation wavelength between about 400 nm and about 430 nm while measuring a first fluorescence intensity at an emission wavelength between about 513 nm and about 540 nm;

exciting the recombinant acetyl-CoA biosensor polypeptide in the cell at a second excitation wavelength between about 460 nm and about 490 nm while measuring a second fluorescence intensity at the emission wavelength; and

normalizing the second fluorescence intensity based on the first fluorescence intensity.

21 . The method of claim 20 , wherein normalizing comprises dividing the second fluorescence intensity by the first fluorescence intensity.

22 . The method of claim 20 , further comprising treating the cell with an acetyl-CoA precursor or nutrient affecting the function of the cell and comparing the normalized fluorescence intensity of the cell to the normalized fluorescence intensity of a control cell.

23 . The method of claim 22 , wherein one or more of a nuclear export signal, a nuclear localization signal, a cytoplasmic localization signal, and a mitochondrial localization signal is attached to an N-terminus of the recombinant acetyl-CoA biosensor polypeptide.

24 . The method of claim 23 , further comprising determining where acetyl-CoA is localized in the cell.

25 . The method of claim 20 , wherein the first excitation wavelength is 405 nm.

26 . The method of claim 20 , wherein the second excitation wavelength is 485 nm.

27 . The method of claim 20 , wherein the emission wavelength is 514 nm.

28 . The method of claim 20 , wherein the providing step comprises transforming the cell with a plasmid comprising a polynucleotide that encodes the recombinant acetyl-CoA biosensor polypeptide.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 10, 2025
From: DIEHL, KATHARINE L.; SMITH, JOSEPH J.
To: UNIVERSITY OF UTAH
Reel/Frame 071977/0496 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 10, 2025
From: UNIVERSITY OF UTAH
To: UNIVERSITY OF UTAH RESEARCH FOUNDATION
Reel/Frame 071978/0165 →
CONFIRMATORY LICENSE Recorded Jan 11, 2024
From: UNIVERSITY OF UTAH
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 066273/0811 →
Continuity (1)
Related Publication 20250052755A1 · Feb 13, 2025
References Cited (18)
US 20160153023A1 · Goodman et al. · 2016 [cited by applicant]
Monteiro DCF, Patel V, Bartlett CP, Nozaki S, Grant TD, Gowdy JA, et al. The structure of the PanD/PanZ protein complex reveals negative feedback regulation of pantothenate biosynthesis by coenzyme A. Chem Biol. Apr. 23… [cited by examiner]
Huttanus HM, Senger RS. A synthetic biosensor to detect peroxisomal acetyl-CoA concentration for compartmentalized metabolic engineering. PeerJ. Sep. 8, 2020;8:e9805. doi: 10.7717/peerj.9805. PMID: 33194349; PMCID: PMC7… [cited by examiner]
Lieberman WK, Brown ZA, Kantner DS, Jing Y, et al.. Chemoproteomics Yields a Selective Molecular Host for Acetyl-CoA. J Am Chem Soc. Aug. 2, 2023;145(30):16899-16905. doi: 10.1021/jacs.3c05489. Epub Jul. 24, 2023. PMID:… [cited by examiner]
Lin W, Mehta S, Zhang J. Genetically encoded fluorescent biosensors illuminate kinase signaling in cancer. J Biol Chem. Oct. 4, 2019;294(40):14814-14822. doi: 10.1074/jbc.REV119.006177. Epub Aug. 21, 2019. PMID: 3143471… [cited by examiner]
BCC Reasearch. Life Science Tools and Reagents: Global Markets Report Overview. Version dated May 19, 2022. Available online at https://web.archive.org/web/20220519080456/https://www.bccresearch.com/market-research/biot… [cited by applicant]
ABCAM. Acetyl COA Assay Kit (ab87546). Version dated Jun. 25, 2022. Available online at https://web.archive.org/web/20220701000000*/https://www.abcam.com/acetyl-coa-assay-kit-ab87546.html (5 pages). [cited by applicant]
Cambronne, X. A., et al. “Biosensor reveals multiple sources for mitochondrial NAD+.” Science 352.6292 (2016): 1474-1477. [cited by applicant]
Greenwald, E. C., et al. “Genetically encoded fluorescent biosensors illuminate the spatiotemporal regulation of signaling networks.” Chemical reviews 118.24 (2018): 11707-11794. [cited by applicant]
Kamphorst, J. J., et al. Quantitative analysis of acetyl-CoA production in hypoxic cancer cells reveals substantial contribution from acetate. Cancer Metab. 2, 23 (2014) (8 pages). [cited by applicant]
Kyte, J. et al. “A Simple Method for Displaying the Hydropathic Character of a Protein.” J. Mol. Biol 157 (1982): 105-132. [cited by applicant]
Monteiro, D. C. F. et al. Formation of a heterooctameric complex between aspartate a-decarboxylase and its cognate activating factor, PanZ, is CoA-dependent. Biochem. Biophys. Res. Commun. 426, 350-355 (2012). [cited by applicant]
Monteiro, D. C. F. et al. The structure of the PanD/PanZ protein complex reveals negative feedback regulation of pantothenate biosynthesis by coenzyme A. Chem. Biol. 22, 492-503 (2015). [cited by applicant]
Pietrocola, F., et al. Acetyl Coenzyme A: A Central Metabolite and Second Messenger. Cell Metab. 21, 805-821 (2015). [cited by applicant]
Ryu, K. W., et al. “Metabolic regulation of transcription through compartmentalized NAD+ biosynthesis.” Science 360.6389 (2018): eaan5780. [cited by applicant]
Shi, L. et al. Acetyl-CoA and the Regulation of Metabolism: Mechanisms and Consequences. Curr. Opin. Cell Biol. 33, 125-131 (2015) (11 pages). [cited by applicant]
Trefely, S. et al. Quantitative subcellular acyl-CoA analysis reveals distinct nuclear metabolism and isoleucine-dependent histone propionylation. Mol. Cell 82, 447-462.e6 (2022). [cited by applicant]
Zhang, S. et al. Metabolic engineering for efficient supply of acetyl-CoA from different carbon sources in [cited by applicant]