We had a similar situation: great diffraction, multiple lattices due to stacked plates that appeared to be single crystals. We ran an additive screen with about a dozen common salts and solvents, e.g., AmSO4, LiCl, MgSO4, AmPO4, PEG400, EG, glycerol, DMSO, etc. at 100 mM for salts or 5-10% for liquids in our best crystallization conditions. AmSO4 and EG changed the crystal form slightly to more blocky plates. Those additives were screened from 50-200 mM and 75 mM AmSO4 was the winner: single crystals that diffracted to 2.4 A, slightly worse than the 2.0 for the stacked plates, but good enough to get a structure.

Cheers.

james09 pruza wrote:
Deal all,
 
Sorry for the non-ccp4 query once again.
I need suggestions regarding the improvement in crystal quality. I have crystallized a protein in MPD. The crystals grow like a thin plates and the plates are stacked together. So, the mosaicity is very high and also indexing is difficult even at 2 angstrom data set.
All suggestions are welcome.
Thanks.
James.
--

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