Debasish

Assuming you do not need seeds, just lift the coverslip, add a small amount of water to the reservoir, close and allow the drop to equilibrate for 20min, or untill you are sure that you have enough liquid to avoid that the drops becomes solid while you pick up the crystals with a loop and transfer to a suitable cryosolution very rich in cryocomponents with very little water.

Improved diffraction? 10% chance!

Enrico.

On Thu, 20 Feb 2014 17:21:53 +0100, Zhijie Li <zhijie...@utoronto.ca> wrote:

Hi Debasish,

I would first use some of those crystals to make seeds and grow some new crystals so that I would not lose the crystal. Dehydration, even done systematically (eg, http://www.mitegen.com/mic_catalog.php?c=jenCrystaloptdehydrate), may or may not improve the diffraction. Like most other things in biological crystallography, it varies from case to case. I do not think other people’s experience really means anything for your crystals.

Zhijie


From: Debasish Chattopadhyay
Sent: Thursday, February 20, 2014 10:59 AM
To: CCP4BB@JISCMAIL.AC.UK
Subject: [ccp4bb] Recovering crystals from dry drops

Would you please share your experience and comments on recovering protein crystals from dry (or almost dry hanging drops) for data collection.


I found some beautiful crystals in hanging drops that were set up three years ago; from the color of the crystals ( the protein binds a colored substrate) and the their shape I know these are crystals of my protein. I had collected data using some of these crystals when they were fresh; resolution was poor and the overall I/sigma was low. I am curious if the dehydration would improve the diffraction now.


Thanks


Debasish




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