Glutamine and Asparagine Side Chain Hyperconjugation-Induced Structurally Sensitive Vibrations
| Autor: | Ryan S. Jakubek, Sanford A. Asher, Zhenmin Hong, Steven J. Geib, Elizabeth M. Dahlburg, David Punihaole |
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| Jazyk: | angličtina |
| Rok vydání: | 2015 |
| Předmět: |
Molecular Structure
Chemistry Stereochemistry Glutamine Water Dihedral angle Hyperconjugation Resonance (chemistry) Spectrum Analysis Raman Article Surfaces Coatings and Films Bond length symbols.namesake Crystallography Protein structure Materials Chemistry symbols Side chain Physical and Theoretical Chemistry Asparagine Deuterium Oxide Raman spectroscopy Ramachandran plot |
| Popis: | We identified vibrational spectral marker bands that sensitively report on the side chain structures of glutamine (Gln) and asparagine (Asn). Density functional theory (DFT) calculations indicate that the Amide III(P) (AmIII(P)) vibrations of Gln and Asn depend cosinusoidally on their side chain OCCC dihedral angles (the χ3 and χ2 angles of Gln and Asn, respectively). We use UV resonance Raman (UVRR) and visible Raman spectroscopy to experimentally correlate the AmIII(P) Raman band frequency to the primary amide OCCC dihedral angle. The AmIII(P) structural sensitivity derives from the Gln (Asn) Cβ-Cγ (Cα-Cβ) stretching component of the vibration. The Cβ-Cγ (Cα-Cβ) bond length inversely correlates with the AmIII(P) band frequency. As the Cβ-Cγ (Cα-Cβ) bond length decreases, its stretching force constant increases, which results in an upshift in the AmIII(P) frequency. The Cβ-Cγ (Cα-Cβ) bond length dependence on the χ3 (χ2) dihedral angle results from hyperconjugation between the Cδ═Oϵ (Cγ═Oδ) π* and Cβ-Cγ (Cα-Cβ) σ orbitals. Using a Protein Data Bank library, we show that the χ3 and χ2 dihedral angles of Gln and Asn depend on the peptide backbone Ramachandran angles. We demonstrate that the inhomogeneously broadened AmIII(P) band line shapes can be used to calculate the χ3 and χ2 angle distributions of peptides. The spectral correlations determined in this study enable important new insights into protein structure in solution, and in Gln- and Asn-rich amyloid-like fibrils and prions. |
| Databáze: | OpenAIRE |
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