Just a thought, Mary - going back to your original question about MPD.  I 
extracted the crystallization conditions from REMARK 280 of 3939 PDB entries a 
couple of years ago.  The average concentration of the MPD used was high - 
38.6%, while PEGs tended to be used at lower concs, e.g. PEG400 25.7%.  You can 
see the data at www.douglas.co.uk/top14.htm 

I thought this information could be useful if you want to replace some of the 
MPD with another precipitant (or cryoprotectant).

Best wishes

Patrick Shaw Stewart


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> -----Original Message-----
> From: CCP4 bulletin board [mailto:[EMAIL PROTECTED] On Behalf Of Mary
> Fitzgerald
> Sent: 09 July 2007 23:05
> To: CCP4BB@JISCMAIL.AC.UK
> Subject: [ccp4bb] Help with reducing crystal mosaicity
> 
> Help please!
> 
> I'm looking for some new ideas.  I have crystals that come out of a
> sitting drop with a mixture of sodium cacodylate at pH 6.5, magnesium
> acetate and MPD for the well solution.  The MPD concentration is
> sufficient to act as a cryoprotectant.  Currently, I directly freeze
> these crystals in liquid nitrogen.  When I collect data, I typically
> have high anisotropic mosaicity; it ranges from 0.8 to 1.2.  This is
> further complicated with a weakly diffracting crystal (4-5 A) that has
> a long unit cell axis of ~500 and often twinning.
> 
> It has been suggested to me that the cryoprotectent is a problem.  I
> haven't checked the diffraction at room temperature, yet.  Please no
> suggestions of finding a different crystal form as that's not a
> consideration at the moment.  I have my reasons.  I did find one
> crystal that has lower mosaicity (0.5 to 0.8) but had weaker
> diffraction then the typical crystal.  Attempts at flash cryoannealing
> have not helped.
> 
> So, what's a good way to change the cryoprotectant if the
> cryoprotectant is the precipitant?  I've considered trying dehydration
> but wasn't certain if that would help with the mosaicity.
> 
> Thanks for any ideas,
> 
> Mary X. Fitzgerald
> Postdoctoral Associate

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