Cooperative and Reciprocal Chiral Structure Formation of an Alanine-Based Peptide Confined at the Surface of Cationic Surfactant Membranes

The confinement of anionic oligoalanine peptides at the surface of cationic membranes can cooperatively reinforce peptide/peptide interactions and induce secondary‐structure formation, and, reciprocally, induce chirality expression of the membrane at the mesoscopic level, thus leading to the formati...

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Veröffentlicht in:Chemistry : a European journal 2011-08, Vol.17 (36), p.9999-10009
Hauptverfasser: Kiagus-Armad, Roni, Brizard, Aurélie, Tang, Claire, Blatchly, Richard, Desbat, Bernard, Oda, Reiko
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container_end_page 10009
container_issue 36
container_start_page 9999
container_title Chemistry : a European journal
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creator Kiagus-Armad, Roni
Brizard, Aurélie
Tang, Claire
Blatchly, Richard
Desbat, Bernard
Oda, Reiko
description The confinement of anionic oligoalanine peptides at the surface of cationic membranes can cooperatively reinforce peptide/peptide interactions and induce secondary‐structure formation, and, reciprocally, induce chirality expression of the membrane at the mesoscopic level, thus leading to the formation of three‐dimensional chiral fibrillar networks. Such a strong binding effect of peptides with cationic membranes and the resulting cooperative assembly behaviors are observed with two different types of cationic surfactant, namely, two‐head two‐tail gemini and one‐head two‐tail surfactants. The ensemble of assembly properties, such as critical micellar concentration (cmc), Krafft temperature (Tk), molecular area at the air/water interface, molecular organization (as studied by FTIR attenuated total reflectance (ATR) measurements and small‐angle X‐ray scattering), and morphology of the aggregates (as observed by optical and electron microscopy studies), are reported. The results clearly demonstrate that the molecular organization and mesoscopic supramolecular structures are controlled by a subtle balance between the peptide/peptide interactions, ionic interactions between the membranes and peptides, and the interactions the between surfactant molecules, which are governed by hydrophobicity and steric interactions. Investigation into such cooperative organization can shed light on the mechanism of supramolecular chirality expression in membrane systems and allow understanding of the structure of peptides in interactions with lipid bilayers. Organized interactions: The cooperative and reciprocal interactions between oligoalanine and nonchiral surfactants are a key factor in their supramolecular structures. Helical ribbons and tubules form in the presence of antiparallel β sheets, whereas twisted ribbons form with parallel β sheets or random coils. Surfactants and peptides only form micelles when disorganized; if they are strongly organized then supramolecular chirality expression is prohibited and platelets are formed (see picture).
doi_str_mv 10.1002/chem.201100828
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Such a strong binding effect of peptides with cationic membranes and the resulting cooperative assembly behaviors are observed with two different types of cationic surfactant, namely, two‐head two‐tail gemini and one‐head two‐tail surfactants. The ensemble of assembly properties, such as critical micellar concentration (cmc), Krafft temperature (Tk), molecular area at the air/water interface, molecular organization (as studied by FTIR attenuated total reflectance (ATR) measurements and small‐angle X‐ray scattering), and morphology of the aggregates (as observed by optical and electron microscopy studies), are reported. The results clearly demonstrate that the molecular organization and mesoscopic supramolecular structures are controlled by a subtle balance between the peptide/peptide interactions, ionic interactions between the membranes and peptides, and the interactions the between surfactant molecules, which are governed by hydrophobicity and steric interactions. 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The ensemble of assembly properties, such as critical micellar concentration (cmc), Krafft temperature (Tk), molecular area at the air/water interface, molecular organization (as studied by FTIR attenuated total reflectance (ATR) measurements and small‐angle X‐ray scattering), and morphology of the aggregates (as observed by optical and electron microscopy studies), are reported. The results clearly demonstrate that the molecular organization and mesoscopic supramolecular structures are controlled by a subtle balance between the peptide/peptide interactions, ionic interactions between the membranes and peptides, and the interactions the between surfactant molecules, which are governed by hydrophobicity and steric interactions. Investigation into such cooperative organization can shed light on the mechanism of supramolecular chirality expression in membrane systems and allow understanding of the structure of peptides in interactions with lipid bilayers. Organized interactions: The cooperative and reciprocal interactions between oligoalanine and nonchiral surfactants are a key factor in their supramolecular structures. Helical ribbons and tubules form in the presence of antiparallel β sheets, whereas twisted ribbons form with parallel β sheets or random coils. 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Organized interactions: The cooperative and reciprocal interactions between oligoalanine and nonchiral surfactants are a key factor in their supramolecular structures. Helical ribbons and tubules form in the presence of antiparallel β sheets, whereas twisted ribbons form with parallel β sheets or random coils. Surfactants and peptides only form micelles when disorganized; if they are strongly organized then supramolecular chirality expression is prohibited and platelets are formed (see picture).</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>21774004</pmid><doi>10.1002/chem.201100828</doi><tpages>11</tpages></addata></record>
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subjects Cations - chemistry
Chemistry
chirality
lipoproteins
Membranes
Membranes - chemistry
oligoalanine
Oligopeptides - chemistry
Peptides
Peptides - chemistry
Scattering, Small Angle
Spectroscopy, Fourier Transform Infrared
Stereoisomerism
structural elucidation
Surface Properties
Surface-Active Agents - chemistry
Surfactants
title Cooperative and Reciprocal Chiral Structure Formation of an Alanine-Based Peptide Confined at the Surface of Cationic Surfactant Membranes
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