I do not have the reference you are seeking, but I have seen cacodylate-containing xtals diffract to better than 1.2 and hold up very well. Also, arsenic has an anomalous signal which may be exploited for phasing, peak ~ 1.04 A.

On 07/29/12 18:53, Tatyana Sysoeva wrote:
Hi!

I heard a couple of times that use of cacodylate buffers in crystallization is bad, and not only because of the compound toxicity.

As I understood, presence of the cacodylate in a protein crystal will cause a particular crystal degradation pattern upon X-ray exposure - "darkening of the crystals, gas formation"
I tried to find some references on that and failed in doing so.
I found some earlier discussions like this one:
http://www.proteincrystallography.org/ccp4bb/message23691.html
but don't have anything to reference in literature. I would appreciate if someone can point me to a right direction.

I am sorry if this question is out of the groups topic range.

Thank you in advance!
Sincerely,
Tanya



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                               modern man in a post-modern world
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