Hi,

I try to crystallize a protein/DNA complex. Is there a general guideline about size / affinity / symmetry of the DNA site? My understanding is that the shorter DNA size preserving strong binding affinity is the better. Is it right? The protein is a homodimer. I have options of using the native asymmetric DNA binding site or a symmetric site derived from sequence concensus. I will try both but I would like to hear your expert comments also. Thank you in advance.

Best,

Joe

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