Computational study of ligand binding in lipid transfer proteins: Structures, interfaces, and free energies of protein-lipid complexes

• Published in: Journal of computational chemistry 2012-08, Vol.33 (22), p.1831-1844
• Main Authors: Pacios, Luis F., Gómez-Casado, Cristina, Tordesillas, Leticia, Palacín, Arantxa, Sánchez-Monge, Rosa, Díaz-Perales, Araceli
• Format: Article
• Language: English
• Subjects: Analytical chemistry; Antigens, Plant - chemistry; Binding Sites; Carrier Proteins - chemistry; electrostatic potential; Ligands; lipid binding; Lipids; Molecular Dynamics Simulation; Molecular structure; Molecules; Plant Proteins - chemistry; Protein Conformation; protein structure; protein-ligand interactions; Proteins; Solubility; solvation effects; Thermodynamics
• ISSN: 0192-8651; 1096-987X
• DOI: 10.1002/jcc.23012

Plant nonspecific lipid transfer proteins (nsLTPs) bind a wide variety of lipids, which allows them to perform disparate functions. Recent reports on their multifunctionality in plant growth processes have posed new questions on the versatile binding abilities of these proteins. The lack of binding specificity has been customarily explained in qualitative terms on the basis of a supposed structural flexibility and nonspecificity of hydrophobic protein‐ligand interactions. We present here a computational study of protein‐ligand complexes formed between five nsLTPs and seven lipids bound in two different ways in every receptor protein. After optimizing geometries in molecular dynamics calculations, we computed Poisson‐Boltzmann electrostatic potentials, solvation energies, properties of the protein‐ligand interfaces, and estimates of binding free energies of the resulting complexes. Our results provide the first quantitative information on the ligand abilities of nsLTPs, shed new light into protein‐lipid interactions, and reveal new features which supplement commonly held assumptions on their lack of binding specificity. © 2012 Wiley Periodicals, Inc. Plant nonspecific lipid transfer proteins bind a broad variety of lipids introducing them into a tunnel‐like cavity in two different orientations without significant structural changes. This versatile ability to bind ligands is analyzed with a number of computational techniques that unveil new features of protein‐lipid interactions.