Dear Anna,
The reprint:-
http://www.sciencedirect.com/science/article/pii/S0020169300822689
has some bearing on your query.
Best wishes,
John
Prof John R Helliwell DSc 
 
 

On 7 May 2012, at 17:30, anna anna <[email protected]> wrote:

> Dear all,
> I'd like some suggestions/opinions about the sense of an experiment proposed 
> by a collaborator expert in saxs.
> In few words, he wants to collect SAXS data on a suspension of protein xtals 
> to investigate "low resolution periodicity" of the xtal (more details below). 
> The experiment requires a very huge number of xtals to obtain the circles 
> typical of saxs and it is very time-consuming to me (I know nothing about 
> saxs, I have only to prepare the sample). I proposed to measure a single 
> rotating xtal (like in XRD) but he told they don't have a goniometer on saxs 
> beamline.
> Here is my concern: does it make sense to measure many xtals together? Don't 
> we lose information with respect to single xtal? And, most of all, what can I 
> see by saxs that I can't see by waxs??
> Sorry for the almost off-topic question but I think that only someone who 
> knows both the techniques can help me!!
> 
> 
> Some detail for who is intrigued by my story:
> we prepared doped magnetite nanoparticles using ferritin as bioreactor. I 
> crystallized this spheres filled with metal and solved the structure at 3.7A 
> but I can see only the protein shell while there is no density inside, even 
> if I know that the nanoparticles are there. A simple explanation is that the 
> particles are free to move in the cavity(note that the diameter of the 
> nanoparticle is shorter then the inner diameter of the protein shell), ie are 
> disordered, and do not contribute to diffraction, in fact, to my knowledge, 
> nobody have ever seen the metal core inside ferritin or dps proteins. 
> However, since they are magnetic particles they must "see" each other through 
> the protein wall, ie they can't be completely free to move in the cavity. 
> Maybe, but this is just my opinion, I don't see the particle because the 
> "period of the particle" in the xtal is different/longer than the period of 
> the protein shell.
> Anyway, we are interested in the relative distance between the magnetic 
> particles in the xtal to study the effects of magnetostatic interactions in 
> nanoparticles 3D arrays. We are going to do this by saxs since, they told me, 
> lower resolution is useful in studying this long range periodicity (the 
> diameter of ferritin is about 120A) but it seems fool to me using a 
> suspension of so many xtals to obtain a scattering curve while I could 
> collect diffraction images from a single xtal!!! I know that saxs is used 
> when you don't have xtals but if you have xtals, ie your system is ordered, 
> xtallography is much more powerful!!
> 
> Another question: how can I handle my diffraction data at 3.7A resolution to 
> "look for" nanoparticles? Should I try a lower symmetry? Maybe the anomalous 
> signal? Have you any reference for a similar case?
> 
> Thank you very much!!
> 
> anna
> 
> 
> 
> 
> 

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