BIGGER is almost always BETTER if you spend the time to do your experiment well, and in particular freezing (flash-cooling) your crystal after an appropriate soak in a good cryo-mixture that is respectful
of your crystal.

Thierry,

X-ray absorption, varies with the wavelength, and by going to shorter wavelengths you can reduce absorption. That will allow you some extra margin before you have a crystal that is too big for X-ray diffraction. At that point you can go to neutron diffraction and position all your hydrogens
too!!

BIGGER is almost always BETTER!

AND

Jürgen,

I never said that you need to look ONLY at large crystals. I just said that once you have extracted as much information as possible from your small crystals, (if possible consolidated a structure at any resolution you can get), by improving your experimental methodology, you should aim towards BIGGER crystals, better Cryo-conditions and that WILL give you higher resolution. Refining a structure at 1.6-1.2A will be much easier than doing it at 3A or lower. The time you spend getting better crystals will save you a lot of time trying to get a decent structure out of bad crystals.

BIGGER is almost always BETTER!

AND

Dirk Kostrewa,

Does stream-cooling beat liquid ethane as well or not?


Enrico.

On Tue, 07 Feb 2012 18:27:04 +0100, Fischmann, Thierry <[email protected]> wrote:


-----Original Message-----
From: CCP4 bulletin board [mailto:[email protected]] On Behalf Of Enrico Stura
Sent: Tuesday, February 07, 2012 11:52 AM
To: [email protected]
Subject: Re: [ccp4bb] Freezing crystal

BIGGER is not always BETTER?

Theoretically it should be better because you have more scattering matter.

Enrico: what you state above is only true if you ignore absorption of the X-ray by the crystal.

Thierry


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