Optically Active Vibrational Spectroscopy of α-Aminoisobutyric Acid Foldamers in Organic Solvents and Phospholipid Bilayers
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
29745985
DOI
10.1002/chem.201801121
Knihovny.cz E-zdroje
- Klíčová slova
- chirality, foldamers, membranes, peptides, vibrational spectroscopy,
- MeSH
- cirkulární dichroismus metody MeSH
- fosfolipidy chemie MeSH
- kyseliny aminoisomáselné chemie MeSH
- lipidové dvojvrstvy chemie MeSH
- molekulární konformace MeSH
- molekulární modely MeSH
- Ramanova spektroskopie metody MeSH
- rozpouštědla chemie MeSH
- sekundární struktura proteinů MeSH
- spektrofotometrie infračervená metody MeSH
- stereoizomerie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- 2-aminoisobutyric acid MeSH Prohlížeč
- fosfolipidy MeSH
- kyseliny aminoisomáselné MeSH
- lipidové dvojvrstvy MeSH
- rozpouštědla MeSH
Helical α-aminoisobutyric acid (Aib) foldamers show great potential as devices for the communication of conformational information across phospholipid bilayers, but determining their conformation in bilayers remains a challenge. In the present study, Raman, Raman optical activity (ROA), infrared (IR) and vibrational circular dichroism (VCD) spectroscopies have been used to analyze the conformational preferences of Aib foldamers in solution and when interacting with bilayers. A 310 -helix marker band at 1665-1668 cm-1 in Raman spectra was used to show that net helical content increased strongly with oligomer length. ROA and VCD spectra of chiral Aib foldamers provided the chiroptical signature for both left- and right-handed 310 -helices in organic solvents, with VCD establishing that foldamer screw-sense was preserved when the foldamers became embedded within bilayers. However, the population distribution between different secondary structures was perturbed by the chiral phospholipid. These studies indicate that ROA and VCD spectroscopies are valuable tools for the study of biomimetic structures, such as artificial signal transduction molecules, in phospholipid bilayers.
Faculty of Life Sciences University of Bradford Bradford West Yorkshire BD7 1DP UK
Manchester Institute of Biotechnology University of Manchester 131 Princess St Manchester M1 7DN UK
School of Chemistry University of Bristol Cantock's Close Bristol BS8 1TS UK
School of Chemistry University of Manchester Oxford Road Manchester M13 9PL UK
School of Science RMIT University GPO Box 2476 Melbourne Victoria 3001 Australia
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