Conformational Flexibility, Internal Hydrogen Bonding, and Passive Membrane Permeability: Successful in Silico Prediction of the Relative Permeabilities of Cyclic Peptides
Autor: | Taha Rezai, Jonathan E. Bock, Matthew P. Jacobson, Chakrapani Kalyanaraman, Mai V. Zhou, R. Scott Lokey |
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Rok vydání: | 2006 |
Předmět: |
Models
Molecular chemistry.chemical_classification Membrane permeability Protein Conformation Hydrogen bond Stereochemistry Molecular Sequence Data Synthetic membrane Solvation Hydrogen Bonding General Chemistry Dielectric Peptides Cyclic Biochemistry Permeability Catalysis Cyclic peptide Colloid and Surface Chemistry Protein structure Membrane chemistry Biophysics Amino Acid Sequence |
Zdroj: | Journal of the American Chemical Society. 128:14073-14080 |
ISSN: | 1520-5126 0002-7863 |
Popis: | We report an atomistic physical model for the passive membrane permeability of cyclic peptides. The computational modeling was performed in advance of the experiments and did not involve the use of "training data". The model explicitly treats the conformational flexibility of the peptides by extensive conformational sampling in low (membrane) and high (water) dielectric environments. The passive membrane permeabilities of 11 cyclic peptides were obtained experimentally using a parallel artificial membrane permeability assay (PAMPA) and showed a linear correlation with the computational results with R(2) = 0.96. In general, the results support the hypothesis, already well established in the literature, that the ability to form internal hydrogen bonds is critical for passive membrane permeability and can be the distinguishing factor among closely related compounds, such as those studied here. However, we have found that the number of internal hydrogen bonds that can form in the membrane and the solvent-exposed polar surface area correlate more poorly with PAMPA permeability than our model, which quantitatively estimates the solvation free energy losses upon moving from high-dielectric water to the low-dielectric interior of a membrane. |
Databáze: | OpenAIRE |
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