Covalent tethering of functional groups to proteins and substrates therefor
View Patent ↗A mutant hydrolase optionally fused to a protein of interest is provided. The mutant hydrolase is capable of forming a bond with a substrate for the corresponding nonmutant (wild-type) hydrolase which is more stable than the bond formed between the wild-type hydrolase and the substrate and has at least two amino acid substitutions relative to the wild-type hydrolase. Substrates for hydrolases comprising one or more functional groups are also provided, as well as methods of using the mutant hydrolase and the substrates of the invention. Also provided is a fusion protein capable of forming a stable bond with a substrate and cells which express the fusion protein.
1. A method for detecting or determining the presence or amount of a mutant dehalogenase polypeptide in a sample comprising the steps of:
a) providing a sample containing a polypeptide comprising said mutant dehalogenase, wherein the mutant dehalogenase has at least 85% amino acid sequence identity to SEQ ID NO:82 and at least two amino acid substitutions, the mutant dehalogenase being capable of forming a bond with a dehalogenase substrate that is more stable than the bond formed between the dehalogenase of SEQ ID NO:82 and the substrate, wherein one substitution is at a residue corresponding to residue 272 of SEQ ID NO:82, and wherein a second substitution is, or wherein second and third substitutions are, at a residue or residues corresponding to residue 175 and/or residue 176 of SEQ ID NO:82;
b) contacting the mutant dehalogenase with a dehalogenase substrate which comprises one or more functional groups; and
c) detecting or determining the presence or amount of the functional group, thereby detecting or determining the presence or amount of the polypeptide.
2. The method of claim 1 , wherein the sample comprises cells comprising the mutant dehalogenase.
3. The method of claim 2 , wherein the cells comprise bacterial cells.
4. The method of claim 2 , wherein the cells comprise mammalian cells.
5. The method of claim 1 , wherein the substrate is a compound of formula (I): R-linker-A-X, wherein: R is one or more functional groups; linker is a group that separates R and A; A-X is a substrate for a dehalogenase; and X is a halogen.
6. The method of claim 5 , wherein the functional group comprises a fluorescent label.
7. The method of claim 5 , wherein A comprises (CH.sub.2).sub.n and n is 4-10.
8. The method of claim 5 , wherein X is Cl.
9. The method of claim 1 , wherein the mutant dehalogenase has at least 90% amino acid sequence identity to SEQ ID NO:82.
10. The method of claim 1 , wherein the substituted amino acid at the position corresponding to amino acid residue 272 is phenylalanine, glycine or alanine.
11. The method of claim 1 , wherein said polypeptide comprises a substituted amino acid at the position corresponding to amino acid residue 176, wherein the substituted amino acid at the position corresponding to amino acid residue 176 is serine, glycine, asparagine, aspartate, threonine, alanine or arginine.
12. The method of claim 1 , wherein said polypeptide comprises a substituted amino acid at the position corresponding to amino acid residue 175, wherein the substituted amino acid at the position corresponding to amino acid residue 175 is methionine, valine, glutamate, aspartate, alanine, leucine, serine or cysteine.
13. The method of claim 1 , wherein said polypeptide comprises substitutions at the position corresponding to amino acid residue 175 and at the position corresponding to amino acid residue 176.
14. The method of claim 1 , further comprising a substitution at the position corresponding to amino acid residue 273.
15. The method of claim 14 , wherein the substituted amino acid at the position corresponding to amino acid residue 273 is leucine, methionine or cysteine.
16. The method of claim 1 , wherein the polypeptide further comprises one or more proteins of interest, thereby yielding a fusion protein.
17. The method of claim 16 , wherein determining the presence or amount of the polypeptide results in determining the presence or amount of the protein of interest.