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. 2023 Mar 30;79(Pt 4):95–104. doi: 10.1107/S2053230X23002224

Table 2. Crystallization.

Method Vapor diffusion
Plate type Sitting drop
Temperature (K) 293
Protein concentration (mg ml−1) 4
Buffer composition of protein solution 50 mM HEPES pH 7.5, 150 mM Li2SO4, 10 mM DTT, 10%(v/v) glycerol, 0.1%(w/v) BOG, 0.02 mM DHT
Composition of reservoir solution 0.1 M HEPES pH 7.5, 500–800 mM sodium citrate, 20%(v/v) ethylene glycol
Volume and ratio of drop 0.75 µl protein solution:0.75 µl reservoir solution
Volume of reservoir (µl) 100

The crystallization method was the same for all five structures reported here.