Experimental Methods in Kinetics (2014)
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1 IIIa- 35 Experimental Methods in Kinetics (2014) Initial examples assume start R = A 0 + B 0 etc., P = 0 follow reaction forward initial rate, etc. measure [A] vs. t Chemical methods: Could mix and take aliquots, to gain time quench reaction (T, ph, some change.. ) then use chemical analysis Problem slow, requires a lot of material Bio applications, chemical methods not work so well, -- often the change studied not chemically very different (folding, enzymology, ligand or membrane binding,.. ) -- Amounts often very limited (problem for chemical anal.) Physical Methods: Monitor Absorbance, fluorescence, ph, pressure, electrochemistry, scattering, whatever is proportional to concentration e.g. Beer-Lambert law: A = bc, A ~ c ph, pressure, conduct. are ~ conc., low conc. I Fluor ~ c Mixing limitations: Mix reagents in a beaker and stir OK for slow reaction Slow reaction pour together and stir takes time k 2 small (seconds) Speed up by reducing size, depend on diffusion - separation
2 IIIa- 36 Fast reaction need - mix fast Faster mix very small volume rapid mixing small mixer, fast flow & turbulence Stopped flow (Atkins Fig ) fill cell quickly from mixer then stop (cell full of fresh mixed reagents) t = 0 Monitor absorbance, fluorescence or other properties Something proportional concentration Stopped-Flow methods idea is rapid mixing, fill/monitor small volume Drive two components (or more) into mixing chamber and out to a cell for monitoring a physical property typically absorbance or fluorescence A B Mixing can occur in about 1 ms, key is turbulence
3 IIIa- 37 Example: Protein folding rapid mix Lipid vesicle + -lactoglobulin, sheet - helix change (Ning Ge, Kinetic Xiuqi traces Zhang, TAK, Biochemistry, for BLG (0.2mg/ml) with DOPG 2010) Ellipticity(mdeg) -10 N 0.15mM DOPG mM DOPG 0.50mM DOPG mM DOPG 2.00mM DOPG Time/s Relative Intensity Circular Dichroism fit to single exponential [A] = [A0]e-kt Kinetics traces of BLG(0.2mg/ml) with DOPG decay in seconds - apparent 1st order lipid~constant mM DOPG 1.00mM DOPG 0.50mM DOPG 0.25mM DOPG 0.15mM DOPG Time/s Fluorescence senses two steps in mechanism, fit to double exponential [A] = [A0]{a e-k t + a e-k t} k1 k2 k3 N I I U fast decay: 100 ms, slower one: seconds like CD Complex process - use this to postulate a mechanism
4 IIIa- 38 Continuous flow measure along flow x t positions in flow successively later in reaction, x t Faster continuous flow, more material Convert distance to time x t possible to get to 100 s or better with micro fluidics Time scales ~1 ms mixing for small volume: ~ 0.1 ml Faster micro mixers micro etch channels flow idea rate limit mix diffuse A,B together D different constant ~ constant shorter distance between A,B (mixing) Same Concept follow conc. [A] vs. t - physical probe determine rate, vary [A] / determine order
5 Example: rapid mix -lactoglobulin+tfe, transition IIIa- 39
6 IIIa- 40 Speed up initiation if photochemical initate A A* then this can be created in very short time Bio-exam: Hb-CO Hb* + CO recombine after photolysis Rhodopsin Rh* --photo absorb cis-trans conform. change Photocycle light pulse trigger, measure rates for spectral changes, e.g. retinal absorbance, can also trap intermediates with cold or other environment Above focus on loss of reagent (or forming product) If reverse reaction or alternate steps important Need to monitor other species (intermediates) Equilibrium - rate depend on forward and reverse step: R & P
7 IIIa- 41 Equilibrium, if elementary A + B k 1 k -1 K e = k 1 /k -1 = C + D r for = r rev [C] e [D] e [A] e [B] e r r r f k k 1 1 [A] [B] [C] [D] = 1 Disturb equilibrium perturbation then relax back to equil. - change T, P, ph, how? discharge capacitor (T),shock wave (P), Laser flash-(ph precursor) or ex. T-jump (laser absorb by solvent) - system relax to new equilibrium - reaction must go forward/reverse to new state (new equil. conc.) Unimolecular case: A k 1 k -1 B A = A e x B = B e + x x = departure from new equilibrium at time = t, new T, P x = x e e -t/ - relaxation time, x 0 at t =, x = x 0 /e at t = r = k 1 A - k -1 B = k 1 (A e -x) - k -1 (B e +x) -da/dt = dx/dt = -(k 1 +k -1 )x + k 1 A e - k -1 B e = -(k 1 +k -1 )x Since at equil. k 1 A e = k -1 B e, can drop 2nd and 3rd terms dx/x = -(k 1 +k -1 )dt ln[x/x 0 ] = -(k 1 +k -1 )t x = x 0 e -t(k 1 +k -1 ) relaxation time: 1/ = k 1 + k -1 Note: relax faster if either k 1 or k -1 fast (same as rate to equil.) (see Derivation 21.4, p.797 in Atkins, Table 7.4 in Tinoco or Engel Ch ) 2 nd order more complex form (hint: x-small, so x 2 very small, neglect quadratic, 2 nd order)
8 IIIa- 42 Since K eq = k 1 /k -1 get both values k 1, k -1 from & K eq Slow T-jump example: Refold Ribonuclease A, FTIR Monitor change 2 frequencies Alternate Example see Engel p.687 RNA conformation Faster Dyer, Callender and co-workers protein and peptide folding with IR or fluorescence See slides Webpage Peptide folding example
9 IIIa- 43 UIC T-jump example: TrpZip2 hairpin with isotope label Labels let us focus on parts of hairpin fold Variation in Temperature Arrhenius behavior
10 IIIa- 44 Helix-Coil mechanism If a polypeptide is helical, then each residue has local ( ) torsions that fit the helical model If it undergoes a transition to a new form, such as a coil, then the local ( ) values change These could occur in a concerted (all together) manner:... hhhhh ccccc... Or more likely in a stepwise pattern:... hhhhh hchhh hcchh... etc.. ccccc... Residues on the termini are more likely to shift from helix to coil due to solvent exposure and lack of H-bond Shows up as activation energy: E a (hhh..-->chh..) < E a (hhh..-->hch..) E a (ccc..-->chc..) < E a (ccc..-->hcc..) So helices are likely to unfold from the termini, or are more likely to fold from center out to ends start unfolded, random coil
11 IIIa- 45 or start fully extended: key is initiate with H-bond formation, center favored: Taken from: Constant Temperature Simulations of Helix Folding SHEN-SHU SUNG,J. Theor.Biol. (1995), 173,
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