[Neutron] Hybrid Method Approaches for Structural Biology session for ACA Meeting
Shuo Qian
qianshuo at gmail.com
Fri Apr 1 17:07:22 CEST 2016
Dear Colleagues,
I want to bring to your attention (and encourage abstract submission) a
session as described below at the American Crystallographic Association
Meeting from July 22 - 26, 2016, in Denver.
The abstract deadline is just extended to April 8th.
Direct link:
http://www.amercrystalassn.org/2016-scientific-program#03.03.01
<http://www.amercrystalassn.org/2016-scientific-program#02.01>
*03.03.01 Hybrid Method Approaches for Structural Biology*
*Organizers: Andrew Howard (howard at agni.phys.iit.edu
<howard at agni.phys.iit.edu>) and Shuo Qian (qians at ornl.gov <qians at ornl.gov>)*
*As the structure and dynamics of biological systems we study are becoming
increasingly complex, with limitations of each individual technology, an
approach of combining multiple methods has to be taken to get a
comprehensive understanding of their biological function. In recent years,
many structural biology tools, including crystallography, small-angle
scattering, cryoelectron microscopy, NMR, and computational simulation are
synergistically applied to challenging systems. In this session, we will
highlight novel and combined methods for structural biology, as well as
application of these methods to important biological systems.*
As neutron scattering especially SANS plays an increasingly important role
in structural biology with other improved techniques, it might be a good
venue to present your latest research on using more than one structural
techniques to understand biology functions. And if you have any questions
please feel free to email me at qians at ornl.gov.
See you at the ACA!
Best Regards,
Shuo
--
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Shuo Qian, Ph.D.
Staff Scientist
Center for Structural Molecular Biology
and Biology and Soft Matter Division
Neutron Science Directorate
Postal Address:
ORNL
PO BOX 2008 MS6430
OAK RIDGE TN 37831-6430
Email: qians at ornl.gov <qianshuo at gmail.com>
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