Fig. 4.
Fig. 4. βS-chain exchange as a function of incubation time with Hb β112 Cys→Asp tetramers. Tetrameric Hb βC112D was incubated with βs chains in 0.1 mol/L phosphate buffer, pH 7.0 at 25°C, and Hb S tetramer formation, as well as generation of β112 Cys→Asp chains, were analyzed by FPLC. (A), (B), and (C) correspond to chromatographic analyses before (zero time point) and after 15 and 30 minutes incubations in the presence of βs chains, respectively. Peaks a, b, c, and d represent β112 Cys→Asp, Hb βC112D, Hb S and βS, respectively. The dotted line is a trace of the gradient profile for NaCl.

βS-chain exchange as a function of incubation time with Hb β112 Cys→Asp tetramers. Tetrameric Hb βC112D was incubated with βs chains in 0.1 mol/L phosphate buffer, pH 7.0 at 25°C, and Hb S tetramer formation, as well as generation of β112 Cys→Asp chains, were analyzed by FPLC. (A), (B), and (C) correspond to chromatographic analyses before (zero time point) and after 15 and 30 minutes incubations in the presence of βs chains, respectively. Peaks a, b, c, and d represent β112 Cys→Asp, Hb βC112D, Hb S and βS, respectively. The dotted line is a trace of the gradient profile for NaCl.

Close Modal

or Create an Account

Close Modal
Close Modal