Petr Kolenko wrote:
Dear all,

I am working on crystallization of a protein purified using intein-chitin binding domain. There is 86% identity with protein with already known high-resolution structure, but I am not able to get any crystals. I heard that reversed phase chromatography is not good for crystallization, e.g. Has anyone of you observed something similar for intein-chitin chromatography? Is there any serious "structural" damage to the target protein during the purification?

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Petr Kolenko
kole...@imc.cas.cz <mailto:kole...@imc.cas.cz>
http://kolda.webz.cz
The failure in crystallisation can be due to so many reasons... including protein damage (ending up with a mixture of components is probably one of the worse cases) Sometimes you need to modify your protein in order to crystallise it, or even use an analog from another organism.

Fred.

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