The circular dichroism (CD) spectrum of an unordered polypeptide chain does not correspond, as has been assumed heretofore, to that of a charged chain such as poly-~glutamic acid or poly-clysine. The latter have been shown to have locally ordered structures with characteristic CD spectra. We have no
Hydrogen-tritium exchange of the random chain polypeptide
β Scribed by S. W. Englander; A. Poulsen
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1969
- Tongue
- English
- Weight
- 807 KB
- Volume
- 7
- Category
- Article
- ISSN
- 0006-3525
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β¦ Synopsis
The hydrogen-tritium exchange character of poly-D,L-alanine was studied in detail aa a model for the hydrogen exchange behavior of the unhindered, polymeric peptide group. The random chain nature of poly-D,L-alanine was evident in the uniformity of exchange rate of all its hydrogens and in the similarity between this rate and that of random chain poly-D,clysine and other known, unhindered secondary amide groups. An equilibrium isotope effect favoring the binding of tritium over protium to the extent of 215'4 was measured. Specific acid and base catalysis of the exchange and the absence of detectable general catalysis were demonstrated. Apparent energy of activation is 17 kcal/mole for deprotonation, largely d1.e to dependence of K , on temperature, and 15 kcal/mole for protonation, which correlates with the extreme apparent pK. The hydrogen-tritium exchange half-time rate of poly-D,calanine a t any pH and temperature (T; "C) is given by the equation: t+ (min) = 200 X 10006T/[lOpH-a + lO3-pHI
π SIMILAR VOLUMES
To investigate the flexibility or motility of the secondary structure of poly-Lglutamic acid, a simple model molecule of proteins, the kinetics of the tritium-hydrogen exchange of this polymer in aqueous solutions waa followed at various pH values by use of a freezedrying technique and a liquid scin