Hi Rhys

Following up on Santosh's post if you are visiting Diamond for your data 
collections we do have a Xenon cell available: 
http://www.diamond.ac.uk/mx-home/Equipment-on-Demand/Xe-Chamber.html

If you want to use it please let your local contact know in advance.

Dave

From: CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] On Behalf Of Santosh 
Panjikar
Sent: 16 January 2014 01:55
To: ccp4bb
Subject: Re: [ccp4bb] Best compounds for heavy atom soaks

Dear Rhys,

You may consider Xenon derivative, which could be prepared simply pressurizing 
the protein crystals in a xenon chamber. It does not require any modification 
of mother liquor. It just needs  cryo-protectant where crystals are stable for 
at least one to two mins. Higher Pressure (20 to 40 bar) and 1-2 min incubation 
time  are normally sufficient for binding of Xenon to proteins.

Xenon binds to pre existing hydrophobic cavities of proteins by dispersion 
force.  Xenon derivatives are highly isomorphous to native crystals. So SIRAS 
phasing could be efficient. However if you consider collecting data at longer 
wavelengths you could get anomalous signal from sulphur too. Weaker SAD or 
SIRAS phases from Xenon derivative could be used to bootstrap the Sulphur 
phasing.

Similarly Kr pressurisation could be tried. MAD experiment can be performed at 
any tunable beamline but the disadvantage with this derivative is, it desorps 
quickly during cooling after pressurisation leaving out with lower than 50-60% 
occupancy.

Success of the Xenon/Krypton derivatisation depends on size of the proteins and 
how stable your
crystals are under cryo-protectant.


The bigger the protein, higher the chance of Xe/Kr binding.


best
Santosh

Santosh Panjikar, Ph.D.
Scientist
Australian Synchrotron
800 Blackburn Road
Clayton VIC 3168
Australia
Ph: +61-4-67770815 (mobile)
      +61-3-85404276 (office)
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