Wei Dai, Hong Yuan, Xiao-Juan Wang, Shu-Qin Gao, Xiangshi Tan and Ying-Wu Lin
RSC Chem. Biol., 2023,4, 330-333
DOI:
10.1039/D3CB00007A,
Communication
Myoglobin (Mb) was found to undergo self-oxidation when a cysteine residue was engineered at position 67 in the heme distal site. Both the X-ray crystal structure and mass spectrum confirmed the formation of a sulfinic acid (Cys–SO2H). Moreover, the self-oxidation could be controlled during protein purification to yield the unmodified form (T67C Mb). Importantly, both T67C Mb and T67C Mb (Cys–SO2H) were able to be labeled by chemicals, which provided useful platforms to generate artificial proteins.