ECTS
6 credits
Component
UFR Chimie-Biologie
Description
Descriptif
The course will present practical and theoretical aspects of the classical approaches used to determine the structure of macromolecules by X-ray crystallography and Nuclear Magnetic Resonance spectroscopy. The program of this course is described below:
Part I - Crystallography - 20h
- Crystallization techniques
- Crystal symmetry and space groups
- Diffraction
- Structure factors, reciprocal space etc
- Tutorial: Data treatment
- Phasing – MIR, SAD, MAD
- Molecular replacement, crystallographic symmetry
- Tutorial: MAD Phasing
- Tutorial: Molecular replacement
- Refinement
- Tutorial: Model building and refinement
- Practical lab: Crystallization on a PSB platform
- Practical lab: X-ray data collection on a ESRF beamline
Part II – Nuclear Magnetic Resonance-20h
- NMR principles: active nuclei, magnetic field, radiofrequency excitation,
return to equilibrium - NMR observables in the spectra of biomolecules (chem. shift, scalar
couplings, linewidth) - NMR observables: measurement
- Practical lab on IBS-NMR platform: data collection
- The steps to structure determination: sample preparation, isotopic labeling
- The steps to structure determination: assignment
- The steps to structure determination: extraction of structural parameters
- Tutorial: Data analysis
- Structure calculation: principles
- Practical lab: Protein structure calculation
Course parts
- UE Structure determination of biological macromolecules - TPPractical work (TP)10h
- UE Structure determination of biological macromolecules - TDTutorials (TD)12h
- UE Structure determination of biological macromolecules - CMLectures (CM)19h
Period
Semester 9
Skills
Decision making in structure determination of biomolecules, expertise in experimental structure determination by X-ray crystallography and liquid-state NMR spectroscopy, critical analysis of structural models at atomic resolution.