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25th European Crystallographic Meeting, ECM 25, İstanbul, 2009 Acta Cryst. (2009). A65, s 81 Page s 81 difference Patterson for the ID31 data at two wavelengths around the Br K edge and also the Pt LIII edge shows up binding site 1 clearly in one of the six samples tested. In order to investigate the detailed binding behaviour we have conducted single crystal analyses with time-resolved freeze quenching after lysozyme single crystal soak times of 10, 90 and 170 minutes. Whilst the quick soaking of 10 minutes, used in our first experiments at ESRF ID31 above, shows clear binding there is a steady progression of increasing binding strength with increasing soak time. Thus, these timeresolved analytical chemistry results show that further heavy atom signal optimizations, and reproducible behaviour, are possible. Prospects for extending our approach to the yet larger isomorphous and wavelength dispersive signal case of Ta6Br12 bound to lysozyme for powder experiments will also be described. Overall, such multi heavy atom cluster compounds like K2PtBr6 and Ta6Br12 offer a way forward to solve de novo protein structures by powder diffraction.

X-ray diffraction study of piezoelectric crystal response on the nanosecond time scale