Prediction of 19F NMR Chemical Shifts in Labeled Proteins: Computational Protocol and Case Study

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• 作者：William C. Isley III ; Andrew K. Urick ; William C. K. Pomerantz ; Christopher J. Cramer
• 刊名：Molecular Pharmaceutics
• 出版年：2016
• 出版时间：July 5, 2016
• 年：2016
• 卷：13
• 期：7
• 页码：2376-2386
• 全文大小：551K
• 年卷期：0
• ISSN：1543-8392

文摘

The structural analysis of ligand complexation in biomolecular systems is important in the design of new medicinal therapeutic agents; however, monitoring subtle structural changes in a protein’s microenvironment is a challenging and complex problem. In this regard, the use of protein-based ¹⁹F NMR for screening low-molecular-weight molecules (i.e., fragments) can be an especially powerful tool to aid in drug design. Resonance assignment of the protein’s ¹⁹F NMR spectrum is necessary for structural analysis. Here, a quantum chemical method has been developed as an initial approach to facilitate the assignment of a fluorinated protein’s ¹⁹F NMR spectrum. The epigenetic “reader” domain of protein Brd4 was taken as a case study to assess the strengths and limitations of the method. The overall modeling protocol predicts chemical shifts for residues in rigid proteins with good accuracy; proper accounting for explicit solvation of fluorinated residues by water is critical.