Abstract
HITHERTO, investigators using the hydrazine method of Akabori and co-workers1 found it necessary to treat the peptides or protein with anhydrous hydrazine at not less than 100° for about 10 hr. in order to break all peptide bonds2–4. This severe treatment causes complete decomposition of cysteine, cystine and poor yields of arginine, aspartic acid and glutamic acid, with the result that they cannot be determined satisfactorily as C-terminal amino-acids. It is now shown that by the addition of an acid catalyst it is possible to decompose peptides under much milder conditions so that all the common amino-acids can be recovered in fair yield.
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References
Akabori, S., Ohno, K., and Narita, K., Bull. Soc. Chem. Japan, 25, 214 (1952).
Locker, R. H., Biochim. Biophys. Acta, 14, 533 (1954).
Niu, C., and Fraenkel-Conrat, H., J. Amer. Chem. Soc., 77, 5882 (1955).
Ohno, K., J. Biochem. Japan, 40, 621 (1953); 41, 345 (1954).
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Fraenkel-Conrat, H., Harris, J. I., and Levy, A. L., in “Methods of Biochemical Analysis”, 2, 360, ed. by Glick (1955).
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BRADBURY, J. An Improvement of the Hydrazine Method for Determination of C-Terminal Amino-acids. Nature 178, 912–913 (1956). https://doi.org/10.1038/178912b0
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DOI: https://doi.org/10.1038/178912b0
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