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29th Mid-Atlantic Protein Workshop This year's workshop began on a Wednesday afternoon and ended Friday midday. Wednesday's keynote lecture by Alasdair Steven of NIH, "Cryo-electron microscopy plus X-ray crystallography: A hybrid approach to visualizing macromolecular interactions and transitions", set the tone for the gathering, in which many structures were described at high resolution, still leaving questions regarding larger biological interactions. Microscopy and other techniques capable of showing large multimolecular assemblies seemed to be one direction in which research is heading. Another clear trend was towards synchrotrons and MAD phasing, usually with selenium. The keynote lecture was followed by dinner by the pond, and a lively poster session.
Meeting Organizer Osnat Herzberg and Keynote speaker Alasdair Steven of NIH In the first of Thursday's sessions, Millie Georgiadis of Rutgers presented several DNA complexes of the Maloney murine leukemia virus reverse transciptase, and Graeme Conn of JHU showed ribosomal protein L11 complexed with a 58-base conserved RNA domain. The T4 gene 59 replication fork binding protein was then presented by Timothy Mueser of NIAMS. The session concluded with two viral integrase structures: Rous sarcoma integrase described by Zhongning Yang of NIAMS and the ASV integrase catalytic core presented by Jacek Lubkowski of NCI. The second session began with Xinhua Ji of NCI, who discussed Hg-MAD phasing. Osnat Herzberg described CARB's structural genomics program and a recent structure emerging from it. The problems of membrane protein crystallography were addressed by Michael Wiener of UVa, and the session ended with Pam Focia of UNC, Chapel Hill surveying the HPRT active site for mechanism and inhibitor discovery.
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Meeting Organizer Gary Gilland and happy attendee David
Davies (NIH)
Amy Swain, Hoffman On Friday there were three in-depth lectures/demonstrations
on the topic of "High-Throughput Structure Determination".
Paul Adams discussed the many-faceted capabilities of the program
CNS (Crystallography and NMR System), Helen Berman gave an update
on the Protein Data Bank and its transition from Brookhaven to
the Research Collaboratory for Structural Bioinformatics (RCSB), and Li-Wei
Hung reviewed the methods and power of the MAD structure-determination
program SOLVE. Before departure, the question of where to convene
next year was discussed. There seemed to be a consensus for holding
the millenial gathering in a new and different place, possibly
away from our usual campuses and laboratories. It's sure to be
good, so stay tuned. |
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