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Martin Spitaler |
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*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** Dear all, in the the light microscopy facility at Imperial College we are recruiting a support staff to help with all aspects of our new super-resolution microscope, from installation to testing, maintenance, quality checks, user training, data handling, data processing, data workflow and integration. The post is funded for one year as part of the BBSRC funding for the microscope. An essential part of the job will be to collaborate with the Bioinformatics Support Service and authors of analysis software (open-source and commercial) to integrate the super-resolution data workflow, e.g. via batch processing tools, Omero scripts etc. Although fixed-term, this is a rather special opportunity to get involved in an exciting super-resolution project in a vibrant research place, and being part of our lively facility, the person can also acquire invaluable experience in all aspects of facility life and light microscopy in biomedical research. For further details see online job description (RB158-13) <https://www4.ad.ic.ac.uk/OA_HTML/OA.jsp?page=/oracle/apps/irc/candidateSelfService/webui/VisVacDispPG&akRegionApplicationId=821&transactionid=579721550&retainAM=Y&addBreadCrumb=S&p_svid=42639&p_spid=1643045&oapc=7&oas=UxchZrWv9Q869aetZmsc1A..>, or contact Stephen Rothery or Martin Spitaler (contact info on FILM website > CONTACTS <http://www3.imperial.ac.uk/imagingfacility/location_contacts>). Deadline for applications is unfortunately already on Wed 18 Dec, interviews will be on or around around Mon-Tue 13-14 January 2014. Best, Martin -- ------------------------------------------------------------------------ *Martin Spitaler, PhD* *FILM - Facility for Imaging by Light Microscopy* - Facility Manager - Sir Alexander Fleming Building, desk 401 Imperial College London / South Kensington Exhibition Road London SW7 2AZ UK Tel. +44-(0)20-759-42023 E-mail [hidden email] <mailto:[hidden email]> Website: http://imperial.ac.uk/imagingfacility |
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John Hyun-2 |
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*****
To join, leave or search the confocal microscopy listserv, go to: http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy ***** To those performing Cryo-EM, You may be interested in a recent article in Nature, (Liao et. al.*). University of California, San Francisco (UCSF) researchers report that they have solved the 3D structure of the TRPV1 ion channel to a near-atomic resolution (3.4 Angstroms) using cry electron microscopy (cryo-EM) employing a Gatan K2 Summit electron counting camera. This marks the first time that the detailed structure of a member of the large and diverse TRP channel family has been solved. ³Ion channels are among the highest potential targets for drug development. Understanding these channels at atomic resolution speeds up the development of powerful therapeutics that modulate the activity of these channels², says Dr. Christopher Booth, Life Science Product Manager at Gatan. ³Until now the 3D structure of ion channels could only be solved using 2D or 3D crystallography, which often required years of painstaking effort to create crystalline samples. This trail blazing work shows that near atomic-resolution structural biology research is now possible without the need for crystallization.² ³Our team has been trying to solve this structure using X-ray crystallography for several years, but we were never able to crystallize the TRPV1 proteins to undertake these kinds of experiments,² says David Julius, professor of physiology at the University of California, San Francisco (UCSF). ³This is the first time we¹ve been able to resolve side chains in membrane proteins without crystallization,² says Yifan Cheng, associate professor of biochemistry and biophysics at UCSF. ³It shows that single-particle cryo-EM can now be used to solve small, low symmetry particles at the highest resolution, and that cryo-EM is applicable to some of the most difficult specimens.² ³This benchmark result is proof that the Gatan K2 Summit electron counting camera is revolutionizing structural biology,² states Dr. Sander Gubbens, Gatan¹s President. ³We are immensely proud that our K2 Summit camera is dramatically expanding the field of cryo-EM and enabling truly novel research.² The K2 Summit is the result of a very successful collaboration between scientists at Gatan, the University of California San Francisco, and the Lawrence Berkeley National Laboratory, with partial funding from the Howard Hughes Medical Institute and the National Science Foundation through an American Recovery and Reinvestment Act Major Instrumentation grant. *Liao M., Cao E., Julius D., Cheng Y., Structure of the TRPV1 ion channel determined by electron cryo-microscopy. Nature, 504 pp.107-112. doi:10.1038/nature12822. See article at: http://www.nature.com/nature/journal/v504/n7478/full/nature12822.html UCSF Press Release: http://www.ucsf.edu/news/2013/12/110571/structure-key-pain-related-protein- unveiled Information on Gatan K2 Summit: http://www.gatan.com/products/digital_imaging/products/K2/index.php -- Best regards, John Hyun Gatan, Inc. Corporate Headquarters 5794 W. Las Positas Blvd. Pleasanton, CA 94588 USA Tel: 1.925.224.7340 Fax: 1.925.463.0204 Email: [hidden email] Website: www.gatan.com On 12/6/13 9:23 AM, "Martin Spitaler" <[hidden email]> wrote: >***** >To join, leave or search the confocal microscopy listserv, go to: >http://lists.umn.edu/cgi-bin/wa?A0=confocalmicroscopy >***** > >Dear all, > > in the the light microscopy facility at Imperial College we are >recruiting a support staff to help with all aspects of our new >super-resolution microscope, from installation to testing, maintenance, >quality checks, user training, data handling, data processing, data >workflow and integration. The post is funded for one year as part of the >BBSRC funding for the microscope. An essential part of the job will be >to collaborate with the Bioinformatics Support Service and authors of >analysis software (open-source and commercial) to integrate the >super-resolution data workflow, e.g. via batch processing tools, Omero >scripts etc. Although fixed-term, this is a rather special opportunity >to get involved in an exciting super-resolution project in a vibrant >research place, and being part of our lively facility, the person can >also acquire invaluable experience in all aspects of facility life and >light microscopy in biomedical research. > > For further details see online job description (RB158-13) ><https://www4.ad.ic.ac.uk/OA_HTML/OA.jsp?page=/oracle/apps/irc/candidateSe >lfService/webui/VisVacDispPG&akRegionApplicationId=821&transactionid=57972 >1550&retainAM=Y&addBreadCrumb=S&p_svid=42639&p_spid=1643045&oapc=7&oas=Uxc >hZrWv9Q869aetZmsc1A..>, >or contact Stephen Rothery or Martin Spitaler (contact info on FILM >website > CONTACTS ><http://www3.imperial.ac.uk/imagingfacility/location_contacts>). > > Deadline for applications is unfortunately already on Wed 18 Dec, >interviews will be on or around around Mon-Tue 13-14 January 2014. > >Best, > >Martin > >-- >------------------------------------------------------------------------ >*Martin Spitaler, PhD* > >*FILM - Facility for Imaging by Light Microscopy* >- Facility Manager - >Sir Alexander Fleming Building, desk 401 >Imperial College London / South Kensington >Exhibition Road >London SW7 2AZ >UK > >Tel. +44-(0)20-759-42023 >E-mail [hidden email] <mailto:[hidden email]> >Website: http://imperial.ac.uk/imagingfacility |
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