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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.
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The peptide bond has partial pi character; its geometry is planar. C is a member of two planes.
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Rotation about Ca sigma bonds: dihedral angles phi and psi psi phi psi phi (yellow arcs)
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Ramachandran plot of allowed dihedral angles. Steric clashes of side chains limit rotation.
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Hydrogen bond network of the alpha helix
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Helix-coil transition, a disruptive view of unraveling
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Nucleation involves adjustment of 6 dihedral angles; elongation, 2
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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…)
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Typical values of and s is approx 0. 001 * s
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Helix macro dipole increases stability for long helices (supports elongation s)
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Zimm-Bragg and Lifson-Roig concepts of weighting
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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
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Chou-Fasman “rules” of biochemistry (probabilities)
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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)
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Helices at work; stable structures perform mechanical tasks in lipid bilayer
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Biotin (+Avidin) measurement tool
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