Barratt Brendon J W, Easton Christopher J, Henry David J, Li Iris H W, Radom Leo, Simpson Jamie S
Research School of Chemistry, Australian National University, Canberra, ACT 0200, Australia.
J Am Chem Soc. 2004 Oct 20;126(41):13306-11. doi: 10.1021/ja046204n.
Peptidylglycine alpha-amidating monooxygenase catalyzes the biosynthesis of peptide hormones through radical cleavage of the C-terminal glycine residues of the corresponding prohormones. We have correlated ab initio calculations of radical stabilization energies and studies of free radical brominations with the extent of catalysis displayed by peptidylglycine alpha-amidating monooxygenase, to identify classes of inhibitors of the enzyme. In particular we find that, in closely related systems, the substitution of glycolate for glycine reduces the calculated radical stabilization energy by 34.7 kJ mol(-1), decreases the rate of bromination with N-bromosuccinimide at reflux in carbon tetrachloride by a factor of at least 2000, and stops catalysis by the monooxygenase, while maintaining binding to the enzyme.
肽基甘氨酸α-酰胺化单加氧酶通过相应激素原C末端甘氨酸残基的自由基裂解催化肽类激素的生物合成。我们将自由基稳定能的从头算计算以及自由基溴化研究与肽基甘氨酸α-酰胺化单加氧酶所表现出的催化程度相关联,以确定该酶的抑制剂类别。特别是我们发现,在密切相关的体系中,用乙醇酸替代甘氨酸可使计算出的自由基稳定能降低34.7 kJ·mol⁻¹,使在四氯化碳中回流时与N-溴代琥珀酰亚胺的溴化速率降低至少2000倍,并使单加氧酶的催化作用停止,同时保持与该酶的结合。