An apparatus for varying the partial pressure of gas in equilibrium wi
th a mounted protein crystal and collecting X-ray diffraction data is
described. This gas cell allows data sets at several different partial
pressures to be collected from the same crystal and is, therefore, we
ll suited for sensitive difference studies. Data have been collected f
rom orthorhombic human hemoglobin A0 crystals at 0 and 406 torr oxygen
to a nominal resolution of 2.8 angstrom using Cu Kalpha radiation (1
torr = 133.32 Pa). The crystals were grown in 11% PEG 8000 at 277 K. T
he crystals were then transferred to 62% PEG 8000 and warmed to 288 K
to match the conditions used in spectroscopic studies of single crysta
ls [Mozzarelli, Rivetti, Rossi, Henry & Eaton (1991). Nature (London),
351, 416-4191. The measured time constant for oxygen binding by hemog
lobin in the gas cell was 174 min. A difference experiment conducted o
n hemoglobin at 0 and 406 torr oxygen pressure yielded data with R(sym
)'s of 5.2 and 6.5%, respectively, and an R factor between data sets o
f 19.5%. Thus, this cell is suitable for determining the structures of
partially ligated hemoglobin.