If metal ion will be sensitive to radiation depends on its redox chemistry
and not its X-ray properties. For a metal to be affected by radiation dose
it needs to be reduced by free radicals. However, such metals are rarely
(by gene counts or deposits in PDB) present in catalytic sites of enzymes.
The most frequently occurring metal ions in catalytic sites e.g. Mg++,
Ca++, Zn++, Fe++, Mn++ lack oxidation state to which they could be reduced
by a single radical. For this reason these metals tend to be very stable
upon radiation and they are last to go. Copper is the counterexample where
radiation sensitivity is much more likely to be expected.

Unfortunately, the original question and part of the discussion involved
generic category of metals involved in catalysis, rather then specific
one.
Magnesium is by far the the most frequently encounter metal in catalytic
sites. In redox reaction the most frequent cofactors are not metals, but
NAD or FAD. Iron is most often present in Fe-S clusters rather than as
standalone Fe++ ion. These clusters are structurally diverse and do not
necessarily participate in catalysis. If they have similar or diverse
sensitivity to radiation is not clear to me.

The question about metal sensitivity to radiation cannot be answered in
general; it needs to be discussed in specific chemical coordination
context.


Separate issue:

The advice about using helical scan is horrible in this context. The
diffraction collected by such method represents state of crystal exposed
to constant high dose. If anything, the helical scan method is more
suitable to study radiation damaged state of the crystal.

Zbyszek Otwinowski

> Dear Dean,
>
> You have already received excellent insight into radiation effects on
> metals. From personal experience, it doesn't take long for the metal
> occupancy to go down to 80%. Of course it is not anywhere near
> "disappearing" but then again, we don't know the details of your data
> collection and of how disappeared are your disappeared metals.
>
> I will only add that you can use modern approaches to data collection to
> minimize the adverse effects of radiation.
>
> 1. Do not chase the highest resolution and try to get what is enough to
> make your enzymologic statements valid. I.e. use less dose.
> 2. If your crystals diffract poorly, consider using several crystals to
> merge few sets of underexposed data.
> 3. For each crystal, use some sort of grid scanning (we call it rastering)
> to estimate the crystal quality. It is implemented on many beamlines
> worldwide. I will insert a shameless plug here and others can follow the
> suite... See Hilgart et al., pages 717-722 here:
> http://journals.iucr.org/s/issues/2011/05/00/issconts.html
> 4. Select the better diffracting regions of the crystal and use "vector"
> or "helical" data collection whereby your crystal is being translated
> along the specified vector as data is being collected. This feature is
> also implemented on number of beamlines, including ours (see the reference
> above).
>
> All these steps are designed for one goal - to spread the total dose over
> as much diffracting volume as possible and thus minimize the damage.
>
> Hope it helps,
> N.
>
> Ruslan Sanishvili (Nukri)
> Macromolecular Crystallographer
> GM/CA@APS
> X-ray Science Division, ANL
> 9700 S. Cass Ave.
> Lemont, IL 60439
>
> Tel: (630)252-0665
> Fax: (630)252-0667
> [email protected]
>
> ________________________________
> From: CCP4 bulletin board [[email protected]] on behalf of Dean
> Derbyshire [[email protected]]
> Sent: Wednesday, April 30, 2014 5:33 AM
> To: [email protected]
> Subject: [ccp4bb] metals disapear
>
> Hi all,
> Has anyone experienced catalytic metal ions disappearing during data
> collection ?
> If so, is there a way of preventing it?
> D.
>
>    Dean Derbyshire
>    Senior Research Scientist
> [cid:[email protected]]
>    Box 1086
>    SE-141 22 Huddinge
>    SWEDEN
>    Visit: Lunastigen 7
>    Direct: +46 8 54683219
>    www.medivir.com<http://www.medivir.com>
>
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Zbyszek Otwinowski
UT Southwestern Medical Center at Dallas
5323 Harry Hines Blvd.
Dallas, TX 75390-8816
Tel. 214-645-6385
Fax. 214-645-6353

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