***  For details on how to be removed from this list visit the  ***
***          CCP4 home page http://www.ccp4.ac.uk         ***



The absorption edges of pure metals are catalogued to about 0.1ev in 10k,
this does not require the use of the 'When you know the distance between 
your sample and detector accurately' clause which I doubt is known with
sufficient certainty.......the XAS people usually hav sets of these foils
and also the FX detector... 

br
________________________________

From: [EMAIL PROTECTED] [mailto:[EMAIL PROTECTED] On Behalf Of
[EMAIL PROTECTED]
Sent: Tuesday, November 29, 2005 5:58 PM
To: [EMAIL PROTECTED]; [email protected]
Subject: Re: [ccp4bb]: ice lattice parameters - was: WHATCHECK Deformation
Matrix - is it advisable to c orrect the cell ?


Once upon a time, quite a while ago, a group of us went to a synchrotron
(which shall remain nameless) to collect data. When we arrived, we found
that due to circumstances beyond our control, or our host's control, the
hutch was empty - no diffractomer, no controls.
 
We decided to take this as a challange and installed the equipment needed to
collect data and indeed collect some data, all in the timeframe of 5 days.
Technically, that would be 5*8*3 hours, of course.
 
One of the things learned that all of us will never forget is this: our
X-ray wavelength was not what we thought it was and the only way to resolve
that issue was to put something in the beam with a known (powder)
diffraction pattern. When you know the distance between your sample and
detector accurately, everything else follows.
 
There are quite a few choices you might consider, and water never occurred
to us at the time because we did not have freezing capabilities. A capillary
with crushed salt (NaCl) crystals works (and will be good for a long time,
provided you do not brake it). Most polymers work and most wax samples you
would use for sealing capillaries work. Basically anything that is
crystalline in nature works.
 
It is probably best to try your experiment at room temperature (stick a
piece of cardboard on the coldstream nozzle for 5 minutes) so you won't have
to worry about cell parameter change with temperature. If you have a lab
source and detector, you can determine ahead of time (and convince yourself)
which sample you want to pack in your synchrotron kit and never remove
again. It is worth carrying.
 
Mark
 
Mark van der Woerd 
BAE SYSTEMS
Huntsville, AL 

-----Original Message-----
From: Edward Berry <[EMAIL PROTECTED]>
To: CCP4BB <[email protected]>
Sent: Tue, 29 Nov 2005 11:54:47 -0800
Subject: [ccp4bb]: ice lattice parameters - was: WHATCHECK Deformation
Matrix - is it advisable to c orrect the cell ?


*** For details on how to be removed from this list visit the *** 
*** CCP4 home page http://www.ccp4.ac.uk *** 
 
I gather the consensus is that we should calculate our cell constants 
assuming the wavelength and crystal-to-film distances are accurate, 
rather than refine them based on what-check output. But if we don't 
quite trust these values (say on our in-house equipment; of course 
the beamline values will be bang-on) it seems to me that ice spots 
and rings would make a good calibration check, if we know the 
correct values for the ice lattice parameters to high accuracy. 
 
This can usually be applied "a posteriori", as most data collection 
trips will probably contain at least one shot of a crystal with 
ice rings, or at least a few spots due to ice toward the end of 
a run (which makes the tell-tale peaks in the wilson plot at 2.26 
and 2.08 nm if they fall close to predicted protein diffraction spots). 
 
Or you can freeze a loop of distilled water and take a shot after 
collecting your best crystal, without changing wavelength or distance. 
But then silver behenate may be better. 
 
Programs exist for fitting diffraction rings, usually to determine 
the beam center, but an accurate resolution is also output. 
 
I found lattice parameters for hexagonal ice in one of the international 
tables: (a=b= 4.5212, c=7.3666 A), and calculated spacings 
3.915, 3.683, 3.457, 2.683, 2.456, 2.261, 2.161, 2.080, and 1.958. 
 
Does anyone have accurate values for these spacings at 100K? 
 
What is the temperature dependence? 
 
Sometimes I get rings at different spacings, which I suspect are 
due to another crystal form of water. The triplet around 3A 
is replaced by a single ring at 3.23. What are the lattice parameters 
for this stuff? 
 
Dirk Kostrewa wrote: 
> Hi Jorge, 
> > I stumbled across the same deformation matrix problem reported by >
WHATCHECK a couple of years ago and initiated a little discussion on the >
CCP4BB, at that time assuming a bug in the program. However, from >
discussions with the author of WHATCHECK, Gerd Vriend, it turned out > that
apparently this deformation matrix resulted from slightly different >
implementations of the same (!) Engh & Huber parameters in WHATCHECK > and,
by that time, in XPLOR/CNS. I can't remember anymore, which of the > bond
lengths came out slightly different. But let's assume, that the C=O > bonds
on average come out slightly longer in your refinement program > compared to
the library used by WHATCHECK (there are some doubts about > the correct
length of the C=O bond in E&H). If you don't have a single > (anti-)parallel
helix bundle or beta-sheet as the only structural > feature of your protein
in the unit cell, then the directions of the > C=O-vectors should be more or
less equally distributed with respect to > your coordinate system, meaning
that also all components of these > vectors along the unit cell axes should
occur with about equal > frequencies. A systematic comparison of the on
average too long C=O-bond > lenghths with the WHATCHECK library value would
then suggest, that your > unit cell dimensions should be decreased by a few
percent, so that after > orthogonalization the refined C=O bonds come out
with the "correct" > slightly shorter average length (I hope, it's not the
other way around > ;-) ). I can't tell you exactly how WHATCHECK does its
analysis, because > the web-site is currently not reachable. As long as the
data processing > was done with great care, personally, I would trust the
refined unit > cell parameters more than the "deformation matrix" analysis
by WHATCHECK. 
> Regarding your question about cryo-temperature bond lenghts, I think, it >
would be time to do a new analysis of ideal bond lenghts of now many > more
very high resolution protein structures whose crystals were > measured at
cryo-temperature to complement the Engh & Huber parameters. 
> (hexagonal, a=b= 4.5212, c=7.3666 A) 
Sorted by resolution 
 
  n h k l d() 
  1 0 0 1 7.367 
  2 1 0 0 3.915 
  3 0 0 2 3.683 
  4 1 0 1 3.457 
  5 1 0 2 2.683 
  6 0 0 3 2.456 
  7 1 1 0 2.261 
  8 1 1 1 2.161 
  9 1 0 3 2.080 
  10 2 0 0 1.958 
  11 1 1 2 1.927 
  12 2 0 1 1.892 
  13 0 0 4 1.842 
  14 2 0 2 1.729 
  15 1 0 4 1.667 
  16 1 1 3 1.663 
  17 2 0 3 1.531 
  18 2 1 0 1.480 
  19 2 1 1 1.451 
  20 1 1 4 1.428 
  21 2 1 2 1.373 
  22 2 0 4 1.341 
  23 3 0 0 1.305 
  24 3 0 1 1.285 
  25 2 1 3 1.268 
  26 3 0 2 1.230 
  27 2 1 4 1.154 
  28 3 0 3 1.152 
  29 2 2 0 1.130 
  30 2 2 1 1.117 
 
 

________________________________

Try the New Netscape Mail Today!
Virtually Spam-Free | More Storage | Import Your Contact List
http://mail.netscape.com 


Reply via email to