Dear colleagues
I’ve got a fully funded PhD studentship (UK only) in my lab and in
collaboration with Prof Dena Lyras at Monash University, and I’m reaching out
to ask for your help in spreading the word.
It's focused on S-layers variants and is a multidisciplinary project, with 2
years at Newca
Dear colleagues
Just wanted to highlight 2 fully funded PhD studentships in my lab with strong
structural biology focus - protein crystallography, cryoEM, cryoET and
combinatorial approaches, combined with biochemistry and microbiology to study
antibiotic-resistant pathogen C. difficile.
Would
Dear all
We have a BBSRC-funded PhD studentship available and would appreciate if you
can circulate to your institutions and potential candidates.
https://www.findaphd.com/phds/project/piercing-the-armour-c-difficile-s-layer-permeability/?p150321
The project builds on our recent work on C. diff
Hi Alan
We got one a few years back, from Fisher, although I think Thermo are the
manufacturer's:
Refrigerator FRCR4504W Forma chromatography THERMO SCIENTIFIC FORMA FRCR4504W
They also arranged for a heavy metal shelf to hold the AKTA as the normal
shelves won't hold the weight.
We only have
Same for Newcastle University, particularly our Faculty of Medical Sciences but
colleagues and labs from across the University.
There are also several efforts to get scientists to help:
http://crowdfightcovid19.org/volunteers
Thanks to all those trying to help!
Paula
On 21 Mar 2020, at 11:5
Dear colleagues
We have been working on a protein that is produced as a pro-peptide, cleaved
internally and reassembled into a complex. The interacting regions are the new
C and N-termini at the cleavage site, so no rearrangement or loss of part of
the protein is involved. The resulting interac
Very well said, Susan! I totally agree and thank you for saying it so clearly
and eloquently!
Best wishes
Paula
===
Dr Paula S. Salgado
Senior Lecturer in Macromolecular Crystallography
Institute for Cell and Molecular Biosciences
Faculty of Medical Sciences
3
)191 208 7432
Fax: +44 (0)191 208 7424
Email: paula.salg...@ncl.ac.uk
From: CCP4 bulletin board on behalf of Paula Salgado
Sent: 03 June 2019 15:47:28
To: CCP4BB@JISCMAIL.AC.UK
Subject: Re: [ccp4bb] 40th CCP4 anniversary competition - 10 Golden Tickets
deadline 18th
We have successfully used non-auxotrophic strains for incorporation of SeMet
and SeCys, with an incorporation level of >80% and no effects on yield or
solubility. Details can be found here:
http://scripts.iucr.org/cgi-bin/paper?S0907444910042022
It's a straight-forward protocol and structure
I recently used Luminorum and was very happy with the result - and they managed
to do it last minute as well!
http://www.luminorum.com/shop/
Paula
===
Dr Paula S. Salgado
Lecturer in Macromolecular Crystallography
Institute for Cell and Molecular Biosciences
Dear colleagues
I have an MRC-funded PhD position currently available in my lab to study
proteins involved in sporulation of the human pathogen Clostridium difficile
(details below).
I would appreciate if you can pass the information to potential students and/or
advertise it in your institution
Dear Anita
One alternative method to determine the thermodynamics and potentially discern
the folding energy changes from the interaction driven ones would be NMR.
Advantages over ITC experiments include: determine if the interaction drives
foldness, estimate associated thermodynamics and, if
Dear all
This is mostly relevant for those of you in the UK, so I apologise for the off
tpopic nature of the email. However, I think this is an important issue for the
CCP4 community as a whole as well, since UK funding changes will affect how
CCP4 is funded and the continued support we all get
Dear Linda
As we described, we used an adapted minimal media to introduce SeCys into our
recombinantly expressed protein. As a SeCys source, we used seleno-cistine
(provided by Sigma) which is reduced to seleno-cysteine and incorporated into
the proteins. It works really well and incorporation
Dear all,
Please find below an ad for a post-doctoral researcher vacancy at
Imperial, posted hereon behalf of Prof Fairweather.
Please reply directly to him or the email refered in the ad.
Best regards
Paula
*Imperial College London, Division of Cell & Molecular Biology, Faculty of
Natural Sc
May I also suggest reading these:
https://intechweb.wordpress.com/2012/01/25/selected-reading-on-research-works-act-why-you-should-care/
https://intechweb.wordpress.com/2012/02/16/open-access-on-a-string-cut-it-and-it-will-grow-back/
Can non-US based scientists sign the petition, btw?
There ar
gards
Dr Paula Salgado
Dear Abhilash
You could try an alternative labelling option: if your protein has
cysteines, try labelling those with selenium. We succeeded in doing this
using non-auxotrophic strains, meaning you deviate less from your native
expression protocol and are therefore more likely to obtain well folded
Another option would be to collect data at the Mn K edge (1.89A) - at this
wavelength Mg has a weak anomalous signal that you should still be able to
detect. I've used Mn K edge to successfully distinguish between Mg, Mn and
Ca ions as well as identify them as ions and not waters by looking at pea
the future.
Best regards
Paula
On 20 October 2010 12:00, Paula Salgado wrote:
> We are still waiting for proofs, so it might be a few weeks before its
> published. If anyone is interested, please email me requesting a preview
> version.
>
> Paula
>
>
> PS: Francois, we did
protein at 1.7A...
Must admit I never had such nice structures before, so I was being extra
careful.
Paula
On 23 November 2010 19:27, Ethan Merritt wrote:
> On Tuesday, November 23, 2010, Paula Salgado wrote:
> > Dear all
> >
> > I'm refining a 33kDa protein model and I
n chain A 2352
Average B value for main chain A 20.651
Average B value for side chain A 21.815
Average B value for whole chain A 21.199
Any help and advice is most appreciated.
Best regards
Paula
We are still waiting for proofs, so it might be a few weeks before its
published. If anyone is interested, please email me requesting a preview
version.
Paula
PS: Francois, we did cite and used your work as starting point.
On 20 October 2010 10:39, francois@cbs.cnrs.fr wrote:
> Hi Paula
>
I would also try non-auxotrophic strains. We have recently had successful
double SeCys + SeMet using BL21. Paper has just been accepted in Acta D,
should be published soon.
Paula
On 18 October 2010 16:05, Yogesh Gupta wrote:
> Does anyone know a commercial source of Cys-auxotroph strain of E.
i from. Does
> that yield a 'command not found'?
>
> Tim
>
> --
> Tim Gruene
> Institut fuer anorganische Chemie
> Tammannstr. 4
> D-37077 Goettingen
>
> GPG Key ID = A46BEE1A
>
>
> On Tue, 19 Jan 2010, Paula Salgado wrote:
>
> > Hi everyo
*#CCP4I MESSAGE Task failed*
I checked and the Coot/bin directory exists and it contains a "findwaters"
executable file.
I should add that doing "find waters" within Coot works fine.
Any ideas? All help welcomed.
Thanks!
Paula
=
2009/12/11 Dale Tronrud
>
>
> Paula Salgado wrote:
> >
> > Actually, I don't think that should be any consolation at all... As
> > scientists, from whatever field, we should be appalled by this kind of
> > mischief from anyone that calls themselves scie
es an appalling image of science and scientists. And of course, is
unethical and wrong...
Today is a sad moment for crystallography and science.
=
Dr Paula Salgado
Division of Molecular Biosciences
Department of Life Sciences
Facul
. If you still
have crystals, run one on a gel and if the MW seems different, you can try
to investigate further. It might mean getting a new, shorter, more
"crystallizable" construct.
Good luck
Paula Salgado
2009/10/11 james09 pruza
> Dear crystallographers,
>
> Sorry for the n
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