摘要

A soluble human O-6-alkylguanine-DNA alkyltransferase (hAGT) chimera was engineered containing the active site of OGT (residues 139-159) and an additional S134P mutation. The resulting hAGT chimera not only retained hAGT%26apos;s ability to repair bulky O-6-alkylene-2%26apos;-deoxyguanosine interstrand cross-linked DNA damage but also displayed enhanced repair of various O-4-alkyl thymidine adducts.

  • 出版日期2013