Protein‐bound conformation of a specific inhibitor against Candida albicans myristoyl‐CoA:protein N‐myristoyltransferase in the ternary complex with CaNmt and myristoyl‐CoA by transferred NOE measurements

• Published in: European journal of biochemistry Vol. 268; no. 18; pp. 4833 - 4841
• Main Authors: Miura, Takaaki, Klaus, Werner, Ross, Alfred, Sakata, Kiyoaki, Masubuchi, Miyako, Senn, Hans
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Science Ltd 01.09.2001
• Subjects: Acyltransferases - antagonists & inhibitors; Acyltransferases - chemistry; Acyltransferases - metabolism; bound conformation; Candida albicans - enzymology; Enzyme Inhibitors - chemistry; Enzyme Inhibitors - metabolism; Enzyme Inhibitors - pharmacology; Inhibitory Concentration 50; Ligands; Magnetic Resonance Spectroscopy; Models, Molecular; myristoyl‐CoA:protein N‐myristoyltransferase; NMR; Protein Binding; Protein Conformation; Stereoisomerism; Substrate Specificity; transferred NOE
• ISSN: 0014-2956; 1432-1033
• DOI: 10.1046/j.1432-1327.2001.02400.x

Transferred nuclear Overhauser enhancement (trNOE) experiments have been performed to study the bioactive conformation(s) of Ro09‐3472/000 derivatives in the ternary complex with Candida albicans myristoyl‐CoA: protein N‐myristoyltransferase (CaNmt) and myristoylCoA (MyrCoA). A critical step in the trNOE study is to identify ‘true’ trNOEs in the spectra. Nonspecific binding of ligands to target proteins and/or spin diffusion effects can give rise to ‘false’ trNOEs, which may lead to an incorrect conclusion if used to derive bound conformations. In this study for all ligands the observed trNOEs arose from specific binding interactions with the active site of CaNmt. This was shown by displacing the ligand with the known tightly binding active‐site inhibitor 1 [Devadas, B., Zupec, M.E., Freeman, S.K., Brown, D.L., Nagarajan, S., Sikorski, J.A., McWherter, C.A., Getman, D. P. & Gordon, J.I. (1995) J. Med. Chem.38, 1837–1840] and measuring the resonance linewidths in the NMR spectrum before and after addition of the competitive inhibitor. The compounds were also tested for nonspecific protein binding with bovine serum albumin (BSA) using the same method. Of the six compounds tested, Ro09‐3700/001 (racemate) and its optically pure enantiomers, Ro09‐4764/001(S) and Ro09‐4765/001(R), showed both specific binding to CaNmt and no interaction with BSA. The NMR data of these molecules in the ternary complex with CaNmt/MyrCoA could thus be used for a detailed structural analysis. Thereby, the conformation of the bound ligand was obtained from a conformational search using the observed trNOEs as a selection filter. The NMR‐determined conformations are in good agreement with the recently solved CaNmt‐bound X‐ray structures of two similar Ro09‐3472/000 derivatives.