Hi Andy,

We were able to use EDX fluorescence scans at a beam line to detect calcium in 
crystals.

https://pubmed.ncbi.nlm.nih.gov/29890074/

It isn't quantitative like micro-pixe but you can see it...

Eddie Snell and Elspeth Garman and team have done some further work on 
micro-pixe, as well – very cool stuff!

https://pubmed.ncbi.nlm.nih.gov/31794207/

Cheers,
Sarah

Sarah EJ Bowman PhD
Associate Research Scientist | Hauptman-Woodward Medical Research Institute
Director | High-Throughput Crystallization Screening Center
Research Associate Professor | Department of Biochemistry | University at 
Buffalo

p: +1 716 898 8623
e: sbowman at hwi.buffalo.edu

Research Webpage<https://hwi.buffalo.edu/scientist-directory/sbowman/>
Crystallization Center Webpage<http://www.getacrystal.org>

Hauptman-Woodward Medical Research Institute
700 Ellicott Street | Buffalo, NY 14203

From: CCP4 bulletin board <CCP4BB@JISCMAIL.AC.UK> on behalf of Andrew Lovering 
<a.lover...@bham.ac.uk>
Reply-To: Andrew Lovering <a.lover...@bham.ac.uk>
Date: Thursday, January 7, 2021 at 9:13 AM
To: "CCP4BB@JISCMAIL.AC.UK" <CCP4BB@JISCMAIL.AC.UK>
Subject: Elemental Analysis

Dear CCP4ers   We have a protein with moderate resolution (mid 2s) with obvious 
metal ion density holding the oligomer together. We can make an educated guess 
that the ions are likely to be Mg/Ca
This sender is trusted.

sophospsmartbannerend
Dear CCP4ers

We have a protein with moderate resolution (mid 2s) with obvious metal ion 
density holding the oligomer together. We can make an educated guess that the 
ions are likely to be Mg/Ca and can look at co-ordination and bond 
lengths…..but I have a more specific question – would it be appropriate to try 
and identify these at the beamline? Obviously the edges for these aren’t 
accessible to sit either side of the peak but perhaps something like micro-pixe 
would be fun; is this done routinely?
https://doi.org/10.1016/j.pbiomolbio.2004.09.005

Best & thanks in advance
Andy


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