Quantum and molecular dynamics study for binding of macrocyclic inhibitors to human α-thrombin

Emilia L. Wu, Ye Mei, KeLi Han, John Zhang

Research output: Contribution to journalArticle

Abstract

Molecular dynamics simulations followed by quantum mechanical calculation and Molecular Mechanics Poisson-Boltzmann Surface Area (MM-PBSA) analysis have been carried out to study binding of proline- and pyrazinone-based macrocyclic inhibitors (L86 and T76) to human α-thrombin. Detailed binding interaction energies between these inhibitors and individual protein fragments are calculated using DFT method based on a new quantum mechanical approach for computing protein-ligand interaction energy. The analysis of detailed interaction energies provides insight on the protein-ligand binding mechanism. Study shows that T76 and L86 bind to thrombin in a very similar "inhibition mode" except that T76 has relatively weaker binding interaction with Glu217. The analysis from quantum calculation of binding interaction is consistent with the MM-PBSA calculation of binding free energy, and the calculated free energies for L86/T76-thrombin binding agree well with the experimental data.

Original languageEnglish (US)
Pages (from-to)4244-4253
Number of pages10
JournalBiophysical Journal
Volume92
Issue number12
DOIs
StatePublished - Jun 2007

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monoethylglycinexylidide
Molecular Dynamics Simulation
Thrombin
Mechanics
Ligands
Proline
Protein Binding
Proteins

ASJC Scopus subject areas

  • Biophysics

Cite this

Quantum and molecular dynamics study for binding of macrocyclic inhibitors to human α-thrombin. / Wu, Emilia L.; Mei, Ye; Han, KeLi; Zhang, John.

In: Biophysical Journal, Vol. 92, No. 12, 06.2007, p. 4244-4253.

Research output: Contribution to journalArticle

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