IP Library Granted Patent US 10,442,842
Granted Patent B2
US 10,442,842 · App. 15/448,282 · Granted Oct 15, 2019

Cleavage resistant photoluminescent proteins and applications thereof

Inventors: Robert R. Beitle (Fayetteville, AR); Rudra Palash Mukherjee (Fayetteville, AR); Suresh K. Thallapuranam (Fayetteville, AR); Joshua Sakon (Fayetteville, AR); David S. McNabb (Fayetteville, AR)
Assignee: The Board of Trustees of the University of Arkansas
C07K14/43595B01D15/08
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Quick Facts
Patent No.
US 10,442,842
App. No.
15/448,282
Granted
Oct 15, 2019
Kind
B2
Abstract

Photoluminescent proteins resistant to protein cleavage reagents are described herein. In being resistant to cleavage reagents, such photoluminesncent proteins can reduce the number of digestion or cleavage products, thereby simplifying quantification and purification of recombinant protein compositions. In some embodiments, a photoluminescent protein described herein comprises an amino acid sequence having an absence of internal methionine residues.

Claims (25)

1. A photoluminescent protein comprising:

an amino acid sequence having an absence of internal methionine residues, wherein each internal methionine residue is substituted with an amino acid inert to cyanogen bromide (CNBr), and at least three internal methionine residues are each substituted by a leucine residue.

2. The photoluminescent protein of claim 1 , wherein the photoluminescent protein is a green fluorescent protein.

3. The photoluminescent protein of claim 2 , wherein the amino acid sequence of the green fluorescent protein includes the sequence of SEQ ID NO:1.

4. The photoluminescent protein of claim 1 , wherein the photoluminescent protein is selected from the group consisting of blue fluorescent protein, cyan fluorescent protein, yellow fluorescent protein and red fluorescent protein and wherein the internal methionine residues are substituted with one or more amino acids inert to CNBr.

5. A recombinant protein composition comprising:

a first amino acid sequence of a target protein; and

a photoluminescent protein coupled to the first amino acid sequence, the photoluminescent protein comprising an amino acid sequence having an absence of internal methionine residues, wherein each internal methionine residue is substituted with an amino acid inert to CNBr and at least three of the substituted amino acids is leucine.

6. The recombinant protein composition of claim 5 , wherein the photoluminescent protein is a green fluorescent protein.

7. The recombinant protein composition of claim 1 , wherein the amino acid sequence of the green fluorescent protein includes the sequence of SEQ ID NO:1.

8. The recombinant protein composition of claim 5 , wherein the photoluminescent protein is selected from the group consisting of blue fluorescent protein, cyan fluorescent protein, yellow fluorescent protein and red fluorescent protein and wherein the internal methionine residues are substituted with one or more amino acids inert to CNBr.

9. A method of purifying recombinant protein composition comprising:

providing a mixture including the recombinant protein composition, the recombinant protein composition comprising a first amino acid sequence of a target protein and a photoluminescent protein coupled to the first amino acid sequence, the photoluminescent protein including an amino acid sequence having an absence of internal methionine residues; and

treating the recombinant protein composition with CNBr to release the recombinant protein from an intact photoluminescent protein.

10. The method of claim 9 , wherein the photoluminescent protein is a green fluorescent protein and wherein the internal methionine residues are substituted with one or more amino acids inert to CNBr.

11. The method of claim 10 , wherein the one or more substitute amino acids is leucine.

12. The method of claim 11 , wherein the amino acid sequence of the green fluorescent protein includes the sequence of SEQ ID NO:1.

13. The method of claim 8 , wherein the photoluminescent protein is selected from the group consisting of blue fluorescent protein, cyan fluorescent protein, yellow fluorescent protein and red fluorescent protein and wherein the internal methionine residues are substituted with one or more amino acids inert to CNBr.

14. The method of claim 8 further comprising separating the recombinant protein from the intact photoluminescent protein.

15. The method of claim 14 , wherein separating comprises loading the recombinant protein and intact photoluminescent protein on a chromatographic column.

16. The photoluminescent protein of claim 1 , wherein the photoluminescent protein substantially retains its native photoluminescent intensity.

17. The photoluminescent protein of claim 2 , wherein the green fluorescent protein is a GPF UV variant.

18. The photoluminescent protein of claim 1 , wherein the photoluminescent protein is substantially free of additional amino acid mutations.

19. A photoluminescent protein comprising:

an amino acid sequence having an absence of internal methionine residues, wherein internal methionine residues are substituted with amino acids inert to cyanogen bromide (CNBr), and the photoluminescent protein retains photoluminescent intensity of an unsubstituted photoluminescent protein comprising the internal methionine residues.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 7, 2017
From: BEITLE, ROBERT R.; MUKHERJEE, RUDRA PALASH; THALLAPURANAM, SURESH K.; SAKON, JOSHUA; MCNABB, DAVID S.
To: THE BOARD OF TRUSTEES OF THE UNIVERSITY OF ARKANSAS
Reel/Frame 042634/0104 →
Continuity (2)
Provisional Application 62302447 · Mar 2, 2016
Related Publication 20170253640A1 · Sep 7, 2017
Cited By (1)
US 12,403,179