ion. And, to me at least, this change makes
no sense. Protein chains with covalently attached glycans are one biochemical,
structural and functional unit.
Best wishes,
Radu
> This suggestion violates a basic principle of data base theory. A
> single data item cannot encode two pieces of
Hi Tobias,For what is worth, we report 1.22 A for single particle cryo-EM ;-)) But very likely there is more in that dataset, we should know soon.Best wishes,RaduOn 9 Jun 2020 3:11 pm, Tobias Beck wrote:Dear all,Thanks a lot! (I should have used the PDB query myself for neutrons, sry, my bad)As th
plasmids are
also available on Addgene. Some extra biotin has to be added to culture medium
in my experience. Examples from our lab (HEK cells) are in PMID: 27418511 and
28817804.
Best wishes,
Radu
> Dear friends in crystallography,
> I know this seems unrelated, but it really isn't
Hi Paul,
Fair point, apologies if anyone was offended by my comments! I simply thought
that such matters are meaningful for this forum. I am just as guilty as
everyone, and it is important to put our work into the broader perspective
from time to time.
Best wishes,
Radu
> Hi Radu and
ny of the structures solved on synchrotrons worldwide and of the
zillions in the PDB are of any use or biological relevance (original
question)? There is an enormous amount of waste, including the nasty chemicals
use to grow crystals and to phase pointless structures, let's be honest.
Best wis
doesn't really ask or
answer biological questions... for these, whether we like it or not,
macromolecular crystallography (or NMR, even in cell) cannot be the future. In
my opinion :-)
Best wishes,
Radu
> Stating the crystallography is dead might be a bit premature, it is still king
> for
for all practical
purposes... then yes, I fully agree :-) It would however be wrong to erase its
historical contribution to understanding biology.
Best wishes,
Radu
> I would wonder more if the biological questions you can *ask* with a (crystal)
> structure are sufficiently relevant to justi
0, or higher,
dilutions in empty (pLEXm or any irrelevant plasmid) to keep total DNA amounts
constant. Is there no hint of monomer whatsoever in your prep?
Best wishes,
Radu
--
Radu Aricescu
MRC Laboratory of Molecular Biology
Francis Crick Avenue
Cambridge Biomedical Campus
Cambridge CB2 0QH
, especially for
membrane and secreted proteins. All vectors are with Addgene, early passage
cells from ATCC.
Best wishes,
Radu
--
Radu Aricescu
MRC Laboratory of Molecular Biology
Francis Crick Avenue
Cambridge Biomedical Campus
Cambridge CB2 0QH, U.K.
tel: +44-(0)1223-267049
fax: +44-(0)1223-268305
Oops,
I made a mistake in my previous email, apologies! Griffithsin would also
require high-Man glycans, so kifunensine treatment or GnTI-/- cells So
yes, it's either PNGase or cryo-EM...
Best wishes,
Radu
> Hi Savvas,
>
> Many Thanks for your inputs and references. This
anyone crystallize proteins
these days anyway :-)
Best wishes,
Radu
--
Radu Aricescu
MRC Laboratory of Molecular Biology
Francis Crick Avenue
Cambridge Biomedical Campus
Cambridge CB2 0QH, U.K.
tel: +44-(0)1223-267049
fax: +44-(0)1223-268305
www: http://www2.mrc-lmb.cam.ac.uk/group-leaders/a-to-g/r
Hi Stefan,
I also owe you an apology for my bad choice of words. One can debate about
usefulness, but Pavel is right, the software is not "bizarre". And, as several
people pointed out, it certainly addresses a need (which I didn't know about).
Mea culpa.
Best wishes,
Radu
>
ervers can only help up to a point...
Best wishes,
Radu
PS: At least, one day, maximum-likelihood refinement programs will deal with
weak data satisfactorily :-) Nobody likes to throw data away.
> Dear all,
>
> to join Pierre's comments on what 'strange' things happen at
so
far, all negative (i.e. thankfully haven't encountered of such accidents). I'm
wondering whether "crystallisation contaminants" might be related to a
particular type of targets, or expression system, or purification
strategies... I'll check the paper Tristan suggested when I ge
ng it a purification tag or whatever.
I suppose this might have happened to somebody you know, hence the motivation
to spend time on the bizarre ContaMiner. Which is a pity, a silly outcome
would only teach people to do their job (or train their robots) properly.
Best wishes,
Radu
--
Radu Arices
70422). Also, I'd use different
systems depending whether the recombinant protein is intended for functional,
fluorescence microscopy, structural analyses (say X-ray vs cryo-EM).
Best wishes,
radu
--
Radu Aricescu
MRC Laboratory of Molecular Biology
Francis Crick Avenue
Cambridge Biomedi
Dear Gerard,
Thank you for the answer, absolutely not a problem! I am very grateful for all
the great software from Global Phasing and I know that support is great.
Enjoying the STARANISO server for example atm.
Best wishes,
Radu
> Dear Radu,
> Nice to know that your problem is
wishes,
Radu
> Hi Radu,
> This may be caused by the coordinates being too many unit cells away from
the
> origin. In COOT you can easily symmetry move coordinates here to a place
closer to the origin.
> Hope this helps,
> Robbie
> Sent from my Windows 10 phone
> Van: r
in.
I tried everything I could think of to fix this, no luck so far I'm
probably making a very silly mistake... But would be very grateful for any
advice!
Best wishes,
Radu
PS: space group is C2
--
Radu Aricescu
MRC Laboratory of Molecular Biology
Francis Crick Avenue
Cambridge Biomedical
risk solving
meaningless structures?
Best wishes,
Radu
--
Radu Aricescu
MRC Laboratory of Molecular Biology
Francis Crick Avenue
Cambridge Biomedical Campus
Cambridge CB2 0QH, U.K.
tel: +44-(0)1223-267049
fax: +44-(0)1223-268305
Original message
>Date: Wed, 12 Apr 2017 10:24:10 +02
Hi JPK,
Not sure about them, but I was a bit surprised to get this ID a couple of years ago: 4COF!
Nice structure nevertheless :-)
Best wishes,
Radu
On 9 Nov 2016 10:40 p.m., "Keller, Jacob" wrote:
>
> I recently was surprised to be looking at a structure with the unfortunate
Dear Herman,
Assuming that the protein is eukaryotic, and glycans N-linked, various ways of
dealing with the issue are described in PMID: 17355862.
Best wishes,
radu
--
A. Radu Aricescu, PhD
MRC Senior Research Fellow
Associate Professor
University of
l if one could harness it!
Best wishes,
radu
--
A. Radu Aricescu, PhD
University Research Lecturer
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of Structural Biology
Roosevelt Drive, Oxford OX3 7BN
United Kingdom
Phone: +44-1865-28
ut of ~200 or more cells in the field? This
does not look like transient expression using a normal plasmid...
Very intriguing nevertheless!
radu
--
A. Radu Aricescu, PhD
University Research Lecturer
University of Oxford
Wellcome Trust Centre for Huma
ience/jobs/303788-Discipline-hopping-internships
or
http://www.york.ac.uk/c2d2/internships/
For informal enquiries contact: radu.caline...@york.ac.uk
--
A. Radu Aricescu, PhD
University Research Lecturer
University of Oxford
Wellcome Trust Centre for Huma
Best place to start:
http://scottlab.ucsc.edu/~wgscott/xtal/wiki/index.php/Crystallography_on_OS_X
--
A. Radu Aricescu, PhD
University Research Lecturer
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of Structural Biology
Or indeed support surreal structures :-))
(PMID: 11853672 vs PMID: 14749821 and so on)
--
A. Radu Aricescu, PhD
University Research Lecturer
MRC Career Development Award Fellow
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of
Hi Jerry,
You may find that pcDNA3.1 won't give you the protein yields needed for
crystallization. Have a look at PMID: 17001101 for an alternative. Your Kozak
sequence looks good,
radu
--
A. Radu Aricescu, PhD
University Research Lecturer
MRC C
, play with deglycosylation conditions etc) and produce a
more homogeneous sample than CHOs (which are leaky, see Chang et al 2007, PMID:
17355862, for details).
Best wishes,
radu
--
A. Radu Aricescu, PhD
University Research Lecturer
MRC Career
bad deal in long term.
Best wishes,
radu
--
A. Radu Aricescu, PhD
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of Structural Biology
Roosevelt Drive, Oxford OX3 7BN
United Kingdom
Phone: +44-1865-287564
Fax: +44-1865-287547
2031) and
many others followed. More recently, people have moved to
transient expression and probably the easiest labelling method
for HEK293 cells can be found in PMID: 17001101.
Best wishes,
radu
------
A. Radu Aricescu, PhD
University of Oxford
Wellcome T
expression, purification and
crystallization are warmly invited to apply :-)
Best wishes,
radu
--
A. Radu Aricescu, PhD
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of Structural Biology
Roosevelt Drive, Oxford OX3 7BN
United Kingdom
truct design (eliminate
Ser/Thr/Pro-rich domains), for other types have a look at
http://www.prozyme.com/pdf/gk80110.pdf for example.
Best wishes,
radu
--
A. Radu Aricescu, PhD
University of Oxford
Wellcome Trust Centre for Human Genetics
Divisi
Dear Vaheh,
I'm not aware of a commercial or cell bank source, but you can get these cells
from HG Khorana's lab at MIT.
Best wishes,
radu
--
A. Radu Aricescu, PhD
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of
Se-Met labelling and so on.
Here are some references (PMID): 17355862, 17001101, 16823037, 11788735,
16082028.
Radu
--
A. Radu Aricescu, PhD
University of Oxford
Wellcome Trust Centre for Human Genetics
Division of Structural Biology
Roosevelt Drive
35 matches
Mail list logo