Detection of a tetrahedral adduct in a trypsin ... - ACS Publications

J. Paul G. Malthouse, Neil E. Mackenzie, Alan S. F. Boyd, and A. Ian Scott. J. Am. Chem. Soc. , 1983, 105 (6), pp 1685–1686. DOI: 10.1021/ja00344a06...
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J . Am. Chem. SOC.1983, 105, 1685-1686

Detection of a Tetrahedral Adduct in a Trypsin-Chloromethyl Ketone Specific Inhibitor Complex by 13C NMR

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J. Paul G. Malthouse,' Neil E. Mackenzie,2 Alan S. F. Boyd,] and A. Ian Scott*2 Department of Chemistry, University of Edinburgh Edinburgh EH9 3JJ, Scotland Center for Biological N M R , Department of Chemistry Texas A&M University, College Station, Texas 77843 Received November 26, I982 X-ray crystallographic studies at 1.9-2.6-A resolution of inhibitor complexes of the serine proteases t r y p ~ i nand ~ . ~subtilisin BPN'S have so far failed to resolve the state of hybridization of the carbonyl group of the inhibitor: Thus, although no significant distortion of carbonyl sp2 hybridization of trypsin inhibitors has yet been revealed by N M R ~ p e c t r o s c o p y participiation ,~~~ of the serine hydroxyl group in covalent bond formation with the proximal carbonyl of inhibitors linked to the neighboring histidine residue is by no means excluded by the crystallographic evidence cited above. In order to resolve this question for the case of a trypsin-inhibitor complex, we have selected Z-lys-CMK (1),8 which specifically alkylates N-3 of h i ~ t i d i n e - 5 7 , ~As J ~ discussed below, clear evidence for a tetrahedral adduct is displayed by the I3NMR spectrum of this inhibitor complex with trypsin. [2-I3C]Z-lys-CMKwas synthesizedgJl from [ l-13C]lysine (90 atom % enrichment). In aqueous solution (pH