[3dem] Virus particles excluded from CryoEM holey grids holes

srinivas mullapudi mullapudi.srinivas at gmail.com
Mon Aug 20 10:06:58 PDT 2012


Dear Daniel,

Try Bacitracin at 10-50 ug/ml. This is a small peptide molecule with
excellent particle dispersion capacity across holes. In our experience,
bacitracin at 10ug/ml has helped us dispersing a variety of protein samples
 on to the grid with out aggregation.

Good Luck
M

Srinivas Mullapudi PhD, CEMT
Principal Consultant
RESSER-G
1800 Austin Parkway #1318
Sugarland TX 77479

On Mon, Aug 20, 2012 at 8:42 AM, LUQUE BUZO, DANIEL <dluque at cnb.csic.es>wrote:

>  Dear all,
> We are having serious problems to obtain high quality cryo-EM holey grids
> of an apparently excellent virus preparation. Find enclosed several cryo-EM
> images taken at different magnifications of the fungal virus preparation we
> are working with. As you can see, virions attach preferentially to the
> carbon surface, whereas holes are almost empty.  We could also observe the
> presence of other larger structures than virions of variable size
> (arrowheads). We suspect that the anomalous behavior of the virus particle
> suspension is due to the presence of these uncharacterized structures.
>
> Particle concentration is routinely tested by negative staining of serial
> dilutions. Although dilution 1/80 is adequate to obtain a reproducible lawn
> of particles by negative staining, we had to use a dilution 1/5 to lay a
> few particles in the holes, ~20-30 particles/hole (as shown in these
> images). We have used many variations in our protocols with negative
> results; we used clean acetone washed grids, with/without glow discharge,
> and Quantifoil and C-flats holey grids with the same results (even using
> undiluted sample). SDS-PAGE and Coomasie staining of the virus preparations
> showed only the viral proteins and no contaminant. We suspect that these
> amorphous structures are related to lipids and/or nucleic acids from the
> virus.
>
> Have anyone had a similar virus sample with this behavior? If so, How can
> we remove these aggregates without altering virus particles? .
>
> You can get the images from this web site:
>
> http://halley.cnb.csic.es/~virus/3dem/CryoEM_problems.jpg
>
> Thanks in advance!
>
> Best regards,
>
> --
>
> Daniel Luque, Ph.D.
> Department of Structure of Macromolecules
> Centro Nacional Biotecnología/CSIC
> Campus de Cantoblanco
> C/ Darwin nº 3.
> 28049 Madrid, Spain
>
>
>
>
>
>
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>
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