抄録
Myosin has 2 mol of the most reactive thiol, named SH1. 1, 2, 4-Trinitrobenzene (TNB), a novel dinitrophenyl (DNP) ating reagent [Takahashi et al. (1983) Chem. Lett. 1445-1448], was found to react only with SH1 without any other amino acid residues in myosin under the conditions used. Its reaction with myosin SH1 was about 30 times faster than that with N-acetylcysteine (NAC). The reaction rate of TNB with SH1 was about twice compared with that of NEM, the most reactive and selective reagent for SH1 so far found, although its rate with NAC was only one sixtieth that of NEM. As to the λmax, of the absorption spectrum of SH1-DNP-myosin, a large red shift of as much as 20 nm was observed compared with low molecular S-DNP derivatives. This red shift disappeared in 8M urea.
This outstanding feature of SH1 modification with TNB was discussed in terms of affinity labeling by interaction with an aromatic amino acid near SH1.
