- which may well be caused by your cryo-protection or flash-cooling procedure.
I'd try to collect a few images at room temperature to see how good the crystals can be and if this procedure can be improved.
To prevent overlaps, it may help to find a way to collect the data with the crystal rotating around the most problematic cell axis, which tends to be the shortest in the crystal. Bent loops might be helpful.

Mark J van Raaij
Dpto de Estructura de Macromoleculas
Centro Nacional de Biotecnologia - CSIC
calle Darwin 3
E-28049 Madrid, Spain
tel. (+34) 91 585 4616
http://wwwuser.cnb.csic.es/~mjvanraaij



On 13 Jul 2017, at 11:13, Keller, Jacob <[log in to unmask]> wrote:

You've got multiple lattices--try seeding approaches mentioned in a recent/current thread.

JPK

-----Original Message-----
From: CCP4 bulletin board [mailto:[log in to unmask]] On Behalf Of ???
Sent: Thursday, July 13, 2017 3:56 AM
To: [log in to unmask]
Subject: [ccp4bb] weird diffraction pattern

hello everyone,
I would like to seek your opinion on my crystal hits. I am working on a helicase

of which the native structure is solved and the all solution statistics are

fine. I am trying to crystallize and solve the structure of the protein/ssDNA

complex. I recently got some hits from commercial screens using sitting drop

vapor diffusion. After crystallization optimization, these crystals diffract

weakly but to 3.2 Angstroms for the longer exposure time. However, when the

crystals rotate between 120 degrees to 180 degrees, the spots become streaky

(attached), no matter the crystals are hexagonal or flaky. I have tried to

determine the structure by molecular replacement method, but the Rwork/Rfree

values are huge (above 0.5) and can’t be reduced further. I suspect the

obtained crystals quality and resulting processed statistics is the reason for

the observed high Rwork/Rfree values. Are there any suggestions?

All comments will be appreciated!

Best,
Chenjun Tang