Dear All:

Many thanks for your commoents and advice.

I will keep them in mind.

Uma

On Thu, Feb 14, 2013 at 7:54 AM, Fischmann, Thierry <
thierry.fischm...@merck.com> wrote:

>  Collect small slices of data (instead of a complete data set) on several
> crystals then merge the data together to get a full data set.****
>
> The slices of must be small enough so that the damage to the S-NO group is
> still very limited on each slice. You may have to play with beam
> attenuation a bit, depending on how fast the degradation occurs.****
>
> ** **
>
> Good luck****
>
> ** **
>
> Thierry****
>
> ** **
>
> *From:* CCP4 bulletin board [mailto:CCP4BB@JISCMAIL.AC.UK] *On Behalf Of *Uma
> Ratu
> *Sent:* Wednesday, February 13, 2013 5:38 PM
>
> *To:* CCP4BB@JISCMAIL.AC.UK
> *Subject:* [ccp4bb] S-nitrosylation protein****
>
> ** **
>
> Dear All:****
>
>  ****
>
> I plan to use X-ray crystallography method to study the S-nitrosylated
> protein structure. ****
>
>  ****
>
> The native protein crystals diffracted to 2A with synchrontron. I now have
> the crystals of S-ntrosylated protein. ****
>
>  ****
>
> Since S-NO moiety appears to be unstable to synchrotron radiation, could
> you advice /  comments on the stratage on the data collection of
> S-nitrosylated protein crystals? ****
>
>  ****
>
> The protein crystals did not diffract well with in house X-ray. ****
>
>  ****
>
> Thank you for your comments. ****
>
>  ****
>
> Uma****
>
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