One-electron reduction of selenomethionine oxide

Experimental evidence is provided that selenomethionine oxide (MetSeO) is more readily reducible than its sulfur analogue, methionine sulfoxide (MetSO). Pulse radiolysis experiments reveal an efficient reaction of MetSeO with one-electron reductants, such as e-aq (k = 1.2 × 1010M-1s-1), CO·-2 (k = 5.9 × 108 M-1s-1) and (CH3)2) C·OH (k = 3.5 × 107M-1s-1), forming an intermediate selenium-nitrogen coupled zwitterionic radical with the positive charge at an intramolecularly formed Se∴ N 2σ/1σ* three-electron bond, which is characterized by an optical absorption with λmax at 375 nm, and a half-life of about 70 μs. The same transient is generated upon HO· radical-induced one-electron oxidation of selenomethionine (MetSe). This radical thus constitutes the redox intermediate between the two oxidation states, MetSeO and MetSe. Time-resolved optical data further indicate sulfur-selenium interactions between the Se∴ N transient and GSH. The Se∴ N transient appears to play a key role in the reduction of selenomethionine oxide by glutathione.