Dear Morgan Elizabeth,

To complete the answers and suggestion made by the ccp4 community, I would add, that you can actually combine the service offered by HTX facility : You send your protein, and they are preparing the crystallization plate for you in CD-plate which may be use in both Harvester and for Direct in-situ data collection (no harvesting, nothing except the X-ray will touch the crystals). The great advantage is that like this, you don't have to be worried by the plate transportation. They are prepared on-site and then if you go for an in-situ experiment, it can be measured on three of the ESRF beamlines. Notably, we can on MASSIF-1 combine in-situ screening then if required automated harvesting directly at the beamline.


Feel free to contact us.

mbow...@embl.fr

didier.nuri...@esrf.fr

marq...@embl.fr


All the best,

Nicolas




On 23/11/2023 10:31, Jose A. MARQUEZ wrote:

Dear Elizabeth,


/In situ/ data collection is a good approach to try in your case. You could use the CrystalDirect technology for automated crystal harvesting that is more gentle to crystals than manual harvesting. This is  available both at EMBL Grenoble and EMBL Hamburg facilities, which offer integrated crystallography services in collaboration with the ESRF and Petra III synchrotrons.


doi:10.3791/62491.

doi:10.1016/j.crmeth.2021.100102.

doi:10.1107/s0907444912031459.


Best wishes


Josan

_________________________________________________________
Jose A. Marquez, Senior Scientist
Head of the Crystallization Facility
European Molecular Biology Laboratory, Grenoble.
Delivery address: EMBL, 71, Avenue des Martyrs
38000 Grenoble, France
Postal address: EMBL, 71, Avenue des Martyrs
CS 90181 38042 Grenoble Cedex 9, France
Phone +33 (0)476 20 74 25
Fax. +33 (0)476 20 71 99

https://www.embl.org/groups/marquez/ https://www.embl.org/services-facilities/grenoble/high-throughput-crystallisation/ https://htxlab.embl.org/ _________________________________________________________
On 11/22/2023 5:44 PM, Blake, Morgan Elizabeth wrote:
Hello!

I am a PhD student working on a crystallography project to wrap up my dissertation research. I have purified a complex of two proteins, and I can consistently grow crystals in 10% PEG3350, 0.2M KSCN, 0.1M BIS-TRIS propane pH 7.5. These crystals have sharp edges and can grow to a large size (greater than 0.5 mm), but the crystals seem to be very fragile. When we open the drops to harvest the crystals, we have little time to harvest the crystals before they crack. When we move the crystals to a cryoprotectant, over time they start fracturing. We've tried using different percentages of glycerol, ethylene glycol, PEG400, and oil for cryoprotectants with no success. Needless to say, the crystals do not diffract well, with spot patterns that look very streaky/mosaic, which I presume is due to the defects that we see in harvesting/handling. We have screened for alternate crystallization conditions, but we seem to get the same morphology in other conditions. Does anyone have suggestions for additives we could use post-crystallization to help stabilize our crystals?

Thanks for your advice!

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--
Nicolas Foos PhD - ARISE fellow
https://orcid.org/0000-0003-2331-8399
EMBL Grenoble, McCarthy Team
71 av. des Martyrs,
38000 Grenoble FRANCE
+33 4 57 42 84 67

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