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Article

Coupling of Functional Hydrogen Bonds in Pyridoxal-5‘-phosphate−Enzyme Model Systems Observed by Solid-State NMR Spectroscopy

Supporting Info

Shasad Sharif,^‡ David Schagen,^‡ Michael D. Toney,^† and Hans-Heinrich Limbach*^‡

Contribution from the Institut fr Chemie und Biochemie, Takustrasse 3, Freie Universitt Berlin, D-14195 Berlin, Germany, and the Department of Chemistry, University of California-Davis, Davis, California 95616

J. Am. Chem. Soc., 2007, 129 (14), pp 4440–4455

DOI: 10.1021/ja066240h

Publication Date (Web): March 20, 2007

‡

Freie Universität Berlin.

†

University of CaliforniaDavis.

In papers with more than one author, the asterisk indicates the name of the author to whom inquiries about the paper should be addressed.

, limbach@chemie.fu-berlin.de

Abstract

We present a novel series of hydrogen-bonded, polycrystalline 1:1 complexes of Schiff base models of the cofactor pyridoxal-5‘-phosphate (PLP) with carboxylic acids that mimic the cofactor in a variety of enzyme active sites. These systems contain an intramolecular OHN hydrogen bond characterized by a fast proton tautomerism as well as a strong intermolecular OHN hydrogen bond between the pyridine ring of the cofactor and the carboxylic acid. In particular, the aldenamine and aldimine Schiff bases N-(pyridoxylidene)tolylamine and N-(pyridoxylidene)methylamine, as well as their adducts, were synthesized and studied using ¹⁵N CP and ¹H NMR techniques under static and/or MAS conditions. The geometries of the hydrogen bonds were obtained from X-ray structures, ¹H and ¹⁵N chemical shift correlations, secondary H/D isotope effects on the ¹⁵N chemical shifts, or directly by measuring the dipolar ²H−¹⁵N couplings of static samples of the deuterated compounds. An interesting coupling of the two “functional” OHN hydrogen bonds was observed. When the Schiff base nitrogen atoms of the adducts carry an aliphatic substituent such as in the internal and external aldimines of PLP in the enzymatic environment, protonation of the ring nitrogen shifts the proton in the intramolecular OHN hydrogen bond from the oxygen to the Schiff base nitrogen. This effect, which increases the positive charge on the nitrogen atom, has been discussed as a prerequisite for cofactor activity. This coupled proton transfer does not occur if the Schiff base nitrogen atom carries an aromatic substituent.

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