1. Bios 532 Circular Dichroism

2. Circular dichroism is a form of chiroptical spectroscopy. Chiroptical spectroscopy uses circularly polarized light, and commonly exploits differences in the interactions of asymmetric chromophores with left- and right-circularly polarized light.

3. Propagates as a plane wave = linear polarization Two plane waves, equal amplitude,  phase is 90  = circular polarization Two plane waves of differing amplitude,  phase is 90  OR Two plane waves, equal amplitude,  phase ≠ 90  = elliptical polarization natural light = unpolarized, propagates in all planes

4. The relationship between CD signal and the Beer-Lambert Law A lcp =  lcp lc for left circularly polarized light (lcp) The definition of CD is  A = A lcp - A rcp =  lcp lc -  rcp lc =  lc Where the difference in absorbance measured is equivalent to , the decadic molar CD.

5. The absorbance change in CD experiments is very small. Modern instruments can measure this value directly, but historically, CD was measured in terms of ellipticity. In the biochemical sciences, CD is commonly still expressed in terms of molar ellipticity, . The relationship between molar ellipticity and the change in absorption coefficient, , is: [  ] = 3298 ∆ 

6. A superposition of vectors of right- and left- circularly polarized light of equal amplitude and phase represents linearly polarized right. When an optically active sample differs in its absorbance for the right vs. left circular light, the resultant amplitude of the more strongly absorbed component will be smaller than that of the less absorbed component. The consequence is that a projection of the resulting amplitude now yields an ellipse instead of the usual line. http://www-structure.llnl.gov/cd/cdtutorial.htm

7. CD is used for proteins because of the chiral nature of the structural features of proteins - Biopolymers are intrinsically asymmetric; L-amino acids predominate over D-amino acids. L-alanine D-alanine Images from onlinediscussion of amino acid chirality: http://opbs.okstate.edu/~Blair/Bioch2344/Chapter7/Chapter7.htm

8. Amino acids Chromophores PHE, TRP, TYR - When an aromatic residue is held rigidly in space, its environment is asymmetric, and it will exhibit circular dichroism. Amide bond In secondary structure conformations, the backbone and the amide bond chromophores are arranged in regular, organized, asymmetric patterns.

9. Near-UV CD spectroscopy is dominated by Phe, Tyr, Trp and disulfides Near UV CD (250 - 350 nm)

10. The amide group is the most abundant CD chromophore in proteins.  * transition~ 190 nm n  * transition~220 nm Far UV CD (180 - 250 nm)

11. Far UV CD exhibits distinct spectra for  -helical,  -sheet, and random coil secondary structure. Brief CD tutorial online: http://www.cryst.bbk.ac.uk/cdweb/html/info_cd.htmlhttp://www.cryst.bbk.ac.uk/cdweb/html/info_cd.html A more detailed tutorial: http://www.newark.rutgers.edu/chemistry/grad/chem585/lecture1.htmlhttp://www.newark.rutgers.edu/chemistry/grad/chem585/lecture1.html

12. CD exhibits characteristic spectra for protein secondary structure features - alpha helix, beta sheet random coil CD spectra can be deconvoluted using a set of basis spectra, but the analysis is difficult and contains bias dependent on the choice of reference spectra. Primary uses for CD: analyze structural changes in a protein upon some perturbation compare the structure of a mutant protein to the parent protein screen candidate proteins for more detailed structural analysis (NMR or X-ray crystallography)

13. apo-myoglobin

14. Green Fluorescent Protein

15. Structure of Lac Repressor