Hi Blake,
You can cross seed and get new condition with good stable crystal
system. Also you could try VMXi beamline, you do not need to use cryo and
use the plate directly.. You have to use Greiner Crystal QuickX ™ or
MiTeGen In-Situ-1 ™ plates.
Thanks Kannan
Show quoted text
On Wed, 22 Nov 2023, 16:54 Blake, Morgan Elizabeth, <[email protected]> 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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