Nucleic acids encoding oxidation-reduction sensitive green fluorescent protein variants
View Patent ↗The disclosure provides proteins that can be used to determine the redox status of an environment (such as the environment within a cell or subcellular compartment). These proteins are green fluorescent protein (GFP) variants (also referred to as redox sensitive GFP (rosGFP) mutants), which have been engineered to have two cysteine amino acids near the chromophore and within disulfide bonding distance of each other. Also provided are nucleic acid molecules that encode rosGFPs, vectors containing such encoding molecules, and cells transformed therewith. The disclosure further provides methods of using the rosGFPs (and encoding molecules) to analyze the redox status of an environment, such as a cell, or a subcellular compartment within a cell. In certain embodiments, both redox status and pH are analyzed concurrently.
1. An isolated nucleic acid molecule encoding a mutant green fluorescent protein (GFP) with a fluorescence spectrum that is sensitive to redox status,
wherein the mutant GFP shares at least 90% sequence identity with SEQ ID NO: 1 and
wherein mutations include:
a) a cysteine at one or both of the residues corresponding to 147 or 149 of SEQ ID NO: 1 and
b) a cysteine at one or both of the residues corresponding to 202 or 204 of SEQ ID NO: 1.
2. The isolated nucleic acid molecule of claim 1 , comprising an expression control sequence.
3. An isolated nucleic acid comprising the isolated nucleic acid molecule of claim 1 functionally linked to a promoter.
4. A purified host cell comprising the isolated nucleic acid of claim 1 .
5. The purified host cell of claim 4 wherein the purified host cell is a bacterial cell, a plant cell, or an animal cell.
6. The purified host cell of claim 4 wherein the purified host cell is a mammalian cell.
7. A method of analyzing an oxidation-reduction condition of or in a purified host cell comprising:
expressing the mutant GFP encoded by the isolated nucleic acid molecule of claim 1 in the purified host cell; and
measuring a fluorescence signal from the mutant GFP, thereby analyzing the oxidation-reduction condition of or in the purified host cell.
8. The method of claim 7 , wherein the mutant GFP is expressed as a fusion protein.
9. The method of claim 7 , further comprising analyzing a pH condition of or in the purified host cell using the mutant GFP.
10. The isolated nucleic acid molecule of claim 1 , comprising mutations selected from the group consisting of:
a) the residues corresponding to 147 and 202 of SEQ ID NO: 1 are cysteine;
b) the residues corresponding to 147 and 204 of SEQ ID NO: 1 are cysteine;
c) the residues corresponding to 149 and 202 of SEQ ID NO: 1 are cysteine;
d) the residues corresponding to 149 and 204 of SEQ ID NO: 1 are cysteine; and
e) the residues corresponding to 147, 149, 202, and 204 of SEQ ID NO: 1 are cysteine.
11. A method of analyzing an oxidation-reduction condition of or in a purified host cell comprising:
expressing the mutant GFP encoded by the isolated nucleic acid molecule of claim 10 in the purified host cell; and
measuring a fluorescence signal from the mutant GFP, thereby analyzing the oxidation-reduction condition of or in the purified host cell.
12. The isolated nucleic acid molecule of claim 10 , comprising an expression control sequence.
13. An isolated nucleic acid comprising the isolated nucleic acid molecule of claim 10 functionally linked to a promoter.
14. A purified host cell comprising an isolated nucleic acid according to claim 10 .
15. The purified host cell of claim 14 wherein the purified host cell is a bacterial cell, a plant cell, or an animal cell.
16. The purified host cell of claim 14 wherein said purified host cell is a mammalian cell.
17. The isolated nucleic acid molecule of claim 1 , comprising the nucleic acid sequence as shown in SEQ ID NO:2, SEQ ID NO:4, SEQ ID NO:6, SEQ ID NO:8, SEQ ID NO:10, or SEQ ID NO:12.