IP Library Granted Patent US 12,158,470
Granted Patent B2
US 12,158,470 · App. 16/765,908 · Granted Dec 3, 2024

Methods and compositions for live cell analysis of intracellular ATP

Inventors: Daniel Appledorn (Ann Arbor, MI); Cicely Schramm (Ann Arbor, MI); Grigory Filonov (Ann Arbor, MI); Kirk Schroeder (Ann Arbor, MI)
Assignee: SARTORIUS BIOANALYTICAL INSTRUMENTS, INC.
G01N33/5735C07K1/082G01N33/542G01N33/582C07K2319/60C12Q2563/107
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Quick Facts
Patent No.
US 12,158,470
App. No.
16/765,908
Granted
Dec 3, 2024
Kind
B2
Abstract

Disclosed herein are ATP biosensor fusion proteins and their use for assaying ATP levels in cells.

Claims (37)

1. A polynucleotide comprising a nucleic acid encoding a fusion protein of genus X1-X2-X3-X4-X5, wherein:

X1 is a FRET acceptor polypeptide consisting of the amino acid sequence of SEQ ID NO: 1, and X5 is a FRET donor polypeptide consisting of the amino acid sequence of SEQ ID NO: 4;

X2 and X4 are selected from the group consisting of (i) X2 is A and X4 is A; (ii) X2 is S and X4 is SA; (iii) X2 is S and X4 is A; (iv) X2 is absent and X4 is GA; (v) X2 is absent and X4 is FF; and (vi) X2 is T and X4 is GTSG; and

X3 is an ATP binding protein consisting of the amino acid sequence of SEQ ID NO: 5;

wherein binding of ATP by the ATP binding protein causes interaction of the FRET acceptor polypeptide and the FRET donor polypeptide.

2. An expression vector comprising the polynucleotide of claim 1 , wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein.

3. A recombinant host cell comprising the expression vector of claim 2 .

4. A kit comprising:

(a) the polynucleotide of claim 1 ; and

(b) a control polynucleotide, wherein the control polynucleotide comprises a nucleic acid encoding a control fusion protein of genus X1-X2-X3-X4-X5, wherein:

X1 is a polypeptide consisting of the amino acid sequence of SEQ ID NO: 1, and X5 is a polypeptide consisting of the amino acid sequence of SEQ ID NO: 4;

X2 and X4 are selected from the group consisting of (i) X2 is A and X4 is A; (ii) X2 is S and X4 is SA; (iii) X2 is S and X4 is A; (iv) X2 is absent and X4 is GA; (v) X2 is absent and X4 is FF; and (vi) X2 is T and X4 is GTSG; and

X3 is a polypeptide consisting of the amino acid sequence of SEQ ID NO: 12.

5. A method of assaying ATP, comprising:

(a) expressing the fusion protein encoded by the polynucleotide of claim 1 in one or more first cells, and generating one or more images selected from the group consisting of:

(i) a fluorescence image generated by detecting fluorescent signals produced by light having the FRET acceptor polypeptide emission wavelength emitted from the one or more first cells upon exposing the one or more first cells to light having the FRET donor polypeptide excitation wavelength;

(ii) a fluorescence image generated by detecting fluorescent signals produced by light having the FRET acceptor polypeptide emission wavelength emitted from the one or more first cells upon exposing the one or more first cells to light having the FRET acceptor polypeptide excitation wavelength;

(iii) a fluorescence image generated by detecting fluorescent signals produced by light having the FRET donor polypeptide emission wavelength emitted from the one or more first cells upon exposing the one or more first cells to light having the FRET donor polypeptide excitation wavelength; and

(iv) any combinations of (i), (ii), and (iii); and

(b) determining a FRET ratio in the one or more first cells by comparing the output of fluorescent signals in the fluorescent image of (i), the fluorescent image of (ii), and/or the fluorescent image of (iii); wherein the level of ATP in the one or more first cells is proportional to the determined FRET ratio.

6. The polynucleotide of claim 1 , wherein X2 is A and X4 is A.

7. The polynucleotide of claim 1 , wherein the fusion protein comprises the amino acid sequence selected from the group consisting of SEQ ID NO: 7, 8, 9, 10, and 11.

8. The kit of claim 4 , wherein the control polynucleotide encodes a control fusion protein comprising the amino acid sequence of SEQ ID NO: 13.

9. The polynucleotide of claim 1 , wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 7.

10. An expression vector comprising the polynucleotide of claim 6 , wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein.

11. An expression vector comprising the polynucleotide of claim 7 , wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein.

12. An expression vector comprising the polynucleotide of claim 9 , wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein.

13. A recombinant host cell comprising the expression vector of claim 10 .

14. A recombinant host cell comprising the expression vector of claim 11 .

15. A recombinant host cell comprising the expression vector of claim 12 .

16. The kit of claim 4 , wherein the polynucleotide encodes a fusion protein, wherein the fusion protein comprises the amino acid sequence selected from the group consisting of SEQ ID NO: 7, 8, 9, 10, and 11.

17. The kit of claim 4 , wherein the polynucleotide encodes a fusion protein, wherein the fusion protein comprises the amino acid sequence of SEQ ID NO: 7.

18. The kit of claim 17 , wherein the control polynucleotide encodes a control fusion protein comprising the amino acid sequence of SEQ ID NO: 13.

19. The kit of claim 4 , wherein (i) the polynucleotide is present in a first expression vector, wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein; and (ii) the control polynucleotide is present in a second expression vector, wherein the control polynucleotide is operatively linked to a promoter sequence capable of directing expression of the control fusion protein.

20. The kit of claim 16 , wherein (i) the polynucleotide is present in a first expression vector, wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein; and (ii) the control polynucleotide is present in a second expression vector, wherein the control polynucleotide is operatively linked to a promoter sequence capable of directing expression of the control fusion protein.

21. The kit of claim 17 , wherein (i) the polynucleotide is present in a first expression vector, wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein; and (ii) the control polynucleotide is present in a second expression vector, wherein the control polynucleotide is operatively linked to a promoter sequence capable of directing expression of the control fusion protein.

22. The kit of claim 18 , wherein (i) the polynucleotide is present in a first expression vector, wherein the polynucleotide is operatively linked to a promoter sequence capable of directing expression of the fusion protein; and (ii) the control polynucleotide is present in a second expression vector, wherein the control polynucleotide is operatively linked to a promoter sequence capable of directing expression of the control fusion protein.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE STATE/COUNTRY PREVIOUSLY RECORDED AT REEL: 059280 FRAME: 0575. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER . Recorded Mar 31, 2022
From: ESSEN INSTRUMENTS, INC.
To: SARTORIUS BIOANALYTICAL INSTRUMENTS, INC.
Reel/Frame 059567/0690 →
MERGER Recorded Mar 16, 2022
From: ESSEN INSTRUMENTS, INC.
To: SARTORIUS BIOANALYTICAL INSTRUMENTS, INC.
Reel/Frame 059280/0575 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 23, 2020
From: SCHRAMM, CICELY; SCHROEDER, KIRK; APPLEDORN, DANIEL; FILONOV, GRIGORY
To: ESSEN INSTRUMENTS, INC. D/B/A ESSEN BIOSCIENCE, INC.
Reel/Frame 052739/0628 →