| 摘要 |
This invention provides an amadoriase having high substrate specificity to fructosyl valyl histidine. Such amadoriase comprises substitution of one or more amino acid residues at positions corresponding to amino acids selected from the group consisting of position 98, position 259, position 154, position 125, position 261, position 263, position 106, position 103, position 355, position 96, position 66, position 67, position 70, position 100, position 110, position 113, position 114, and position 156 in the amadoriase derived from the genus Coniochaeta. This invention enables accurate measurement of α-fructosyl valyl histidine derived from the β-chain amino terminus in glycated hemoglobin in the presence of ε-fructosyl lysine. |
| 主权项 |
1. A modified amadoriase comprising an amino acid sequence that is at least 95% identical to the amino acid sequence as shown in SEQ ID NO: 1, and comprising one or more amino acid substitutions at positions corresponding to the amino acid sequence of SEQ ID NO: 1, selected from the group consisting of:
(a) substitution of glutamic acid at position 98 with glutamine, histidine, lysine, arginine, glycine, alanine, valine, isoleucine, leucine, methionine, cysteine, serine, threonine, asparagine, aspartic acid, phenylalanine, tyrosine, or tryptophan; (b) substitution of valine at position 259 with alanine, cysteine, or serine; (c) substitution of serine at position 154 with glycine, tyrosine, asparagine, glutamine, aspartic acid, glutamic acid, histidine, or cysteine; (d) substitution of histidine at position 125 with alanine, leucine, phenylalanine, tyrosine, asparagine, glutamine, glutamic acid, lysine, or arginine; (e) substitution of tyrosine at position 261 with alanine, leucine, phenylalanine, tryptophan, or lysine; (f) substitution of glycine at position 263 with lysine, arginine, histidine, aspartic acid, or glutamic acid; (g) substitution of aspartic acid at position 106 with an amino acid having a lower molecular weight than aspartic acid, selected from the group consisting of glycine, alanine, serine, valine, threonine, cysteine, leucine, isoleucine, and asparagine; (h) substitution of glycine at position 103 with lysine, arginine, or histidine; (i) substitution of alanine at position 355 with lysine, arginine, histidine, aspartic acid, or glutamic acid; (j) substitution of aspartic acid at position 96 with alanine, asparagine, histidine, or serine; (k) substitution of lysine at position 66 with glycine and/or valine at position 67 with proline; (l) substitution of glutamine at position 70 with proline; (m) substitution of threonine at position 100 with arginine; (n) substitution of glutamine at position 110 with alanine, leucine, methionine, phenylalanine, tryptophan, asparagine, histidine, lysine, or arginine; (o) substitution of alanine at position 113 with glutamic acid or lysine; (p) substitution of leucine at position 114 with lysine or arginine; and (q) substitution of aspartic acid at position 156 with asparagine, wherein the modified amadoriase exhibits: (i) a lower reactivity to ε-fructosyl lysine relative to the reactivity to α-fructosyl valyl histidine compared with an amadoriase comprising the amino acid sequence as shown in SEQ ID NO: 1; or (ii) a lower reactivity to ε-fructosyl lysine relative to the reactivity to α-fructosyl valine compared with an amadoriase comprising the amino acid sequence as shown in SEQ ID NO: 1. |
