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Re: [ccp4bb] MAD wavelength |
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- Protein crystallographyMain steps:- Protein purification- Crystallisation Special:- Programs for crystallography- X-ray detectors Basic tutorials:- Chemistry- Protein - Peptide - Amino Acids Xtal community:- CCP4BB |
CCP4bb navigationCCP4bb <-- 1999 <-- November 1999 <-- 30 November 1999Subject: Re: MAD wavelength From: Jürgen_Bosch jubosch {- at -} JHSPH {- dot -} EDU Date: 2009-07-16 On a different note,it seems as if SeMet is not a regular experiment in your lab. So I would recommend not to burn your crystals and rather sacrifice the resolution versus loosing your SeMet anomalous signal after couple of degrees into the data collection. It would also be wise to run Mosflm STRATEGY ANOMALOUS to figure out where you should start collecting your data. Good luck, Jürgen On Jul 16, 2009, at 1:15 PM, Jerry McCully wrote: > Dear All: > > Next week we are going to try some seleno-Met labeled crystals. > > We checked the literature to try to find out the peak > wavelength that has been used for SAD or MAD data collection. But > they are slightly different ( may be 50 ev) in different papers. > > I guess this is due to the discrepancy between the fluorescence > scanning and the theoretical vaules of f' and f''. > > When we collect the data, which wavelength should we use? > Should we trust the scanning results? > > Thanks a lot for your comments. > > All the best, > > Jerry McCully > > > > Insert movie times and more without leaving Hotmail®. See how. - Jürgen Bosch Johns Hopkins Bloomberg School of Public Health Department of Biochemistry & Molecular Biology Johns Hopkins Malaria Research Institute 615 North Wolfe Street, W8708 Baltimore, MD 21205 Phone: +1-410-614-4742 Lab: +1-410-614-4894 Fax: +1-410-955-3655 http://web.me.com/bosch_lab/ CCP4bb navigationCCP4bb <-- 1999 <-- November 1999 <-- 30 November 1999 |
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