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Helix-Coil Transition Theory: from biophysics to biochemistry via probability ~ Lauraine Dalton Protein primary, secondary, tertiary structure. Alpha helix.

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Presentation on theme: "Helix-Coil Transition Theory: from biophysics to biochemistry via probability ~ Lauraine Dalton Protein primary, secondary, tertiary structure. Alpha helix."— Presentation transcript:

1 Helix-Coil Transition Theory: from biophysics to biochemistry via probability ~ Lauraine Dalton Protein primary, secondary, tertiary structure. Alpha helix secondary structure properties. Historical development of helix-coil transition theory (HCTT); from chemical physics to empirical biochemistry. Helices at work; selected examples.

2 The peptide bond has partial pi character; its geometry is planar. C  is a member of two planes.

3 Rotation about Ca sigma bonds: dihedral angles phi and psi psi phi psi phi (yellow arcs)

4 Ramachandran plot of allowed dihedral angles. Steric clashes of side chains limit rotation.

5 Hydrogen bond network of the alpha helix

6 Helix-coil transition, a disruptive view of unraveling

7 Nucleation involves adjustment of 6 dihedral angles; elongation, 2

8 Nucleation (difficult) & Propagation (facile) The equilibrium constant for nucleation (sigma) is typically 1000 times lower than for propagation (s). (…cccchhhcccc….)  s = (…ccccccccccc….) and the equilibrium constant (statistical weight) for adding another helical segment at the end of a stretch of helical residues is (….ccchhhhhhhhccc…) s = (….ccchhhhhhhcccc…)

9 Typical values of  and s  is approx 0. 001 * s

10 Helix macro dipole increases stability for long helices (supports elongation s)

11 Zimm-Bragg and Lifson-Roig concepts of weighting

12 Sharpness of the transition, as calculated by Schellman in 1958 A = coexistence of hhh and ccc intermediate states; B = h or c all or none C = infinitely long helix

13 Chou-Fasman “rules” of biochemistry (probabilities)

14 Helix initation and termination in proteins J & D Richardson focused on Ncap and Ccap in analysis of 215 helical segment in known structures. Current view is that Ncap motif consists of four residues S(T)XXE(D) = hydroxyl-XX- carboxylate. Carboxylate (-) interacts favorably with helix macro dipole (+) Ccap contributors are misfits; P (bulky ring) and G (no side chain; 2 H; very flexible)

15 Helices at work; stable structures perform mechanical tasks in lipid bilayer

16 Biotin (+Avidin) measurement tool

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