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EMBO Conference on Protein Synthesis and Translational Control

EMBO Conference on Protein Synthesis and Translational Control

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<str<strong>on</strong>g>EMBO</str<strong>on</strong>g> <str<strong>on</strong>g>C<strong>on</strong>ference</str<strong>on</strong>g> <strong>on</strong> <strong>Protein</strong> <strong>Synthesis</strong> <strong>and</strong> Translati<strong>on</strong>al C<strong>on</strong>trol<br />

EMBL Heidelberg, 9 – 13 September 2009<br />

14:30 - 14:45 Alena Paleskava<br />

14:45 - 15:00 James Munro<br />

Max Planck Institute for Biophysical Chemistry,<br />

Germany<br />

Unusually tight binding of Sec-tRNASec to<br />

the el<strong>on</strong>gati<strong>on</strong> factor SelB due to the<br />

specific recogniti<strong>on</strong> of the selenocysteyl<br />

group by the GTP-bound form 16<br />

Weill Cornell Medical College, United States of<br />

America<br />

Single-molecule observati<strong>on</strong>s of<br />

rate-limiting c<strong>on</strong>formati<strong>on</strong>al events during<br />

ribosomal translocati<strong>on</strong> 17<br />

15:00 - 15:15 Shashi Bhushan<br />

15:15 - 15:30 C. Axel Innis<br />

15:30 - 15:45 Kristen Bartoli<br />

15:45 - 16:00 Erik Böttger<br />

16:00 - 16:30 Coffee Break<br />

Gene Cemter, LMU Munich, Germany<br />

Visualizati<strong>on</strong> of nascent chains in the<br />

ribosomal exit tunnel: Implicati<strong>on</strong> for<br />

sec<strong>on</strong>dary structure formati<strong>on</strong> 18<br />

Yale University, United States of America<br />

Shedding Light Onto Nascent<br />

Chain-Mediated Translati<strong>on</strong>al Stalling 19<br />

University of Pittsburgh, School of Medicine, United<br />

States of America<br />

Novel Role for Mitotic Microtubule Motor<br />

<strong>Protein</strong> Eg5 in <strong>Protein</strong> Translati<strong>on</strong> 20<br />

Institute of Medical Microbiology, Switzerl<strong>and</strong><br />

Aminoglycoside Ototoxicity <strong>and</strong> <strong>Synthesis</strong><br />

of New Compounds with Altered<br />

Drug-Target Interacti<strong>on</strong> 21<br />

iv

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