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. An isolated polynucleotide encoding a mutant dehalogenase having at least 85% amino acid sequence identity to SEQ ID NO:82, and having at least two amino acid substitutions, the mutant dehalogenase 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 an amino acid residue corresponding to residue 272 of SEQ ID NO:82, and wherein a second substitution is at an amino acid residue corresponding to residue 273 of SEQ ID NO: 82.
2. The polynucleotide of claim 1 wherein the mutant dehalogenase has at least 90% amino acid sequence identity to SEQ ID NO: 82.
3. The polynucleotide of claim 1 wherein the amino acid at the position corresponding to residue 272 is phenylalanine, glycine or alanine.
4. The polynucleotide of claim 1 wherein the amino acid at position 273 is leucine, methionine or cysteine.
5. The polynucleotide of claim 1 further comprising a substitution at the position corresponding to amino acid residue 175.
6. The polynucleotide of claim 5 wherein the amino acid at position 175 is methionine, valine, glutamate, aspartate, alanine, leucine, serine or cysteine.
7. The polynucleotide of claim 1 further comprising a substitution at the position corresponding to amino acid residue 176.
8. The polynucleotide of claim 7 wherein the amino acid at the position corresponding to residue 176 is serine, glycine, asparagine, aspartate, threonine, alanine or arginine.
9. The polynucleotide of claim 1 further comprising an open reading frame for one or more proteins of interest, such that expression of the polynucleotide yields a fusion protein comprising the mutant dehalogenase and the protein of interest.
10. A method of expressing the polynucleotide of claim 1 in a host cell, comprising the step of transforming or transfecting the host cell with an expression vector comprising the polynucleotide of claim 1 wherein the polynucleotide is expressed and wherein the encoded mutant dehalogenase polypeptide is produced.
11. The method of claim 10 wherein the host cell is a bacterial cell.
12. The method of claim 10 wherein the host cell is a mammalian cell.