The aim is to collect high resolution cryo data of a number of antiviral compounds complexed to different serotypes of human rhinoviruses. Background: Human rhinoviruses (HRV) account for a majority of the common colds. Although a number of crystal structures of several rhino-viral serotypes and their complexes with anti-rhinoviral compounds have elucidated many structural features important for inhibition, quantitative studies correlating the activities of these anti-virals with the crystal structures of their complexes have not been reported. One of the main reasons is the lack of availability of a large data base of well-refined crystal structures of these complexes. High sensitivity of rhinovirus crystals to radiation damage at room temperatures has resulted in incomplete data sets of limited resolution and quality. Consequently, it has not been possible to refine the structures. Moreover, it required several hundred crystals typically to collect one data set. This limited the number of complexes that could be studied. Cryo data sets from rhinovirus crystals extend to beyond 2A and show much better completeness. Besides, only one crystal is required to collect a complete data set. It is proposed to collect high resolution cryo diffraction data from several HRV serotypes complexed to different anti-viral compounds in order to correlate quantitatively the activities of these compounds with the crystal structures of their complexes. Monochromatic cryo-diffraction data sets from crystals of different HRV serotypes will be collected and processed.

Project Start
1999-08-15
Project End
2000-08-14
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
8
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Chicago
Department
Type
DUNS #
225410919
City
Chicago
State
IL
Country
United States
Zip Code
60637
Durbin, S M; Clevenger, T; Graber, T et al. (2012) X-ray pump optical probe cross-correlation study of GaAs. Nat Photonics 6:111-114
Neutze, Richard; Moffat, Keith (2012) Time-resolved structural studies at synchrotrons and X-ray free electron lasers: opportunities and challenges. Curr Opin Struct Biol 22:651-9
Horsman, Geoff P; Ke, Jiyuan; Dai, Shaodong et al. (2006) Kinetic and structural insight into the mechanism of BphD, a C-C bond hydrolase from the biphenyl degradation pathway. Biochemistry 45:11071-86