scholarly journals Temperature Jump Kinetic Studies of the Binding of Imidazole by Sperm Whale Metmyoglobin

1965 ◽  
Vol 240 (6) ◽  
pp. 2437-2441
Author(s):  
Warren F. Diven ◽  
Douglas E. Goldsack ◽  
Robert A. Alberty
1966 ◽  
Vol 241 (11) ◽  
pp. 2653-2660
Author(s):  
Douglas E. Goldsack ◽  
Wolfgang S. Eberlein ◽  
Robert A. Alberty
Keyword(s):  

1976 ◽  
Vol 153 (2) ◽  
pp. 279-285 ◽  
Author(s):  
S B Brown ◽  
M Shillcock ◽  
P Jones

An investigation of the behavior of protoporphyrin IX, deuteroporphyrin IX, haematoporphyrin IX and coproporphyrin III in aqueous solution revealed extensive and complex aggregation processes. Protoporphyrin appears to be highly aggregated under all conditions studied. At concentrations below 4 μM, aggregation of deutero-, haemato- and coproporphyrin is probably restricted to dimerization. At approx. 4muM each of these three porphyrins exhibits sharp changes in spectra consistent with a “micellization” process to form large aggregates of unknown size. This critical concentration increases with increasing temperature and pH, but is not very sensitive to variation in ionic strength. Temperature-jump kinetic studies on deuteroporphyrin also imply an initial dimerization process, the rate constants for which are comparable with those for various synthetic porphyrins, followed by a further extensive aggragation. The ability of a particular porphyrin to dimerize appears to parallel that of the corresponding iron(III) complexes (ferrihaems), although it is thought that ferrihaems do not exhibit further aggregation under these conditions.


1974 ◽  
Vol 143 (2) ◽  
pp. 353-363 ◽  
Author(s):  
Patricia J. Harrigan ◽  
David R. Trentham

The kinetics of the acylation of d-glyceraldehyde 3-phosphate dehydrogenase from pig muscle by 1,3-diphosphoglycerate in the presence of NAD+ has been analysed by using the relaxation temperature-jump method. At pH7.2 and 8°C the rate of acylation of the NAD+-bound (or holo-) enzyme was 3.3×105m−1·s−1 and the rate of phosphorolysis, the reverse reaction, was 7.5×103m−1·s−1. After a temperature-jump perturbation the equilibrium of NAD+ binding to the acyl-enzyme was re-established more rapidly than that of the acylation. The rate of phosphorolysis of the apoacylenzyme from sturgeon muscle and of aldehyde release from the d-glyceraldehyde 3-phosphate–apoenzyme complex were ≤40m−1·s−1 and ≤12s−1 respectively at pH8.0 and 22°C, which means that both processes are too slow to contribute significantly to the reaction pathway of the reversible NAD+-linked oxidative phosphorylation of d-glyceraldehyde 3-phosphate. Phosphorolysis of both acyl-apoenzyme and acyl-holoenzyme was first-order in Pi up to 100mm-Pi and more. PO43− could be the reactive species of the phosphorolysis of the acyl-holoenzyme, in which case phosphorolysis is a diffusion-controlled reaction, although other kinetically indistinguishable rate equations for the reaction are possible.


1965 ◽  
Vol 240 (11) ◽  
pp. 4312-4315
Author(s):  
Douglas E. Goldsack ◽  
Wolfgang S. Eberlein ◽  
Robert A. Alberty
Keyword(s):  

1962 ◽  
Vol 40 (9) ◽  
pp. 1786-1797 ◽  
Author(s):  
A. Froese ◽  
A. H. Sehon ◽  
M. Eigen

The kinetics of protein–dye and antibody–hapten reactions were studied with the temperature-jump method. The systems used consisted of (i) bovine serum albumin (BSA) and the dye 1-naphthol-4-[4-(4′-azobenzene azo)phenyl arsonic acid], referred to as N—R′, (ii) BSA and the dye 1-naphthol-2-sulphonic acid-4-[4-(4′-azobenzene azo)phenyl arsonic acid], referred to as NS—R′, and (iii) rabbit antibodies to phenyl arsonic acid [Ab] and the hapten N—R′.Each of the systems exhibited a single relaxation time. From the analysis of the concentration dependence of the relaxation times, it was concluded that each system could be represented by the reactions[Formula: see text]where P refers to BSA or Ab, and D to N—R′ or NS—R′. The following rate constants were calculated for the three systems at 25 °C:[Formula: see text]The effects of temperature and pH on the rate constants of the system BSA – N—R′ are discussed.


1989 ◽  
Vol 60 (2) ◽  
pp. 231-236 ◽  
Author(s):  
J. J. Smith ◽  
J. A. McCray ◽  
M. G. Hibberd ◽  
Y. E. Goldman

1960 ◽  
Vol 82 (22) ◽  
pp. 5951-5952 ◽  
Author(s):  
Manfred Eigen ◽  
Gordon G. Hammes

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