Indeed, XChem people have found that it’s rarely NOT possible to make the 
crystal tolerate at least some DMSO – it just “just” requires systematic 
testing.


From: CCP4 bulletin board <[email protected]> On Behalf Of Jon Cooper
Sent: 22 May 2026 14:17
To: [email protected]
Subject: Re: [ccp4bb] Fragment soaking protein crystals with small molecules

Going back to the original question and my apologies if this is obvious, but 
re: "I aliquot the compounds onto pedestal of sitting drop trays then wait for 
the DMSO to evaporate before adding my cryo-protectant solution and pre-grown 
protein crystals." I was wondering if there is any scope to use DMSO as the 
cryoprotectant then you wouldn't have to wait so long (if at all) for it to 
evaporate? I guess you have tested this. I remember the XChem people were very 
keen on having DMSO in everything about a decade ago.
Best wishes, Jon Cooper (Emeritus at UCL) 
[email protected]<mailto:[email protected]>
Erratum and other hopefully useful things: https://crxp.org.uk


Sent from Proton Mail<https://proton.me/mail/home> for Android.


-------- Original Message --------
On Friday, 05/22/26 at 08:02 Weiss, Manfred 
<[email protected]<mailto:[email protected]>>
 wrote:

Dear Leon,



you may want to check out the workflow at your F2X facility in Berlin.



hz-b.de/F2X



In particular, the paper in JoVE by Wollenhaupt et al. should be interesting

for you 
(https://www.jove.com/de/t/62208/workflow-tools-for-crystallographic-fragment-screening-at-helmholtz)

You are welcome to contact us offline, if you have more questions.

Best wishes
Manfred

________________________________
From: CCP4 bulletin board <[email protected]<mailto:[email protected]>> 
on behalf of Giang, Leon (MU-Student) 
<[email protected]<mailto:[email protected]>>
Sent: Tuesday, May 12, 2026 6:16 PM
To: [email protected]<mailto:[email protected]>
Subject: [ccp4bb] Fragment soaking protein crystals with small molecules

Hello everyone,

I am looking for advice on my fragment soaking protocol. Recently, I obtained a 
crystal structure of a small molecule within my protein. These compounds are 
insoluble in aqueous solution so I've been preparing aliquots of the compound 
at known concentrations in 100% DMSO.  I aliquot the compounds onto pedestal of 
sitting drop trays then wait for the DMSO to evaporate before adding my 
cryo-protectant solution and pre-grown protein crystals. I am trying to 
reproduce my results with different concentrations of compound but have to wait 
a long time for the DMSO to evaporate. I am looking for advice on how to speed 
up the DMSO evaporation.

Thanks,
Leon

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