Double Smectic Self-Assembly in Block Copolypeptide Complexes

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Unit:
Department of Chemistry
Title:
Double Smectic Self-Assembly in Block Copolypeptide Complexes
Languages of Item:
English
Abstract:
We show double smectic-like self-assemblies in the solid state involving alternating layers of different polypeptide α-helices. We employed rod-coil poly(γ-benzyl l-glutamate)-block-poly(l-lysine) (PBLG-b-PLL) as the polymeric scaffold, where the PLL amino residues were ionically complexed to di-n-butyl phosphate (diC4P), di(2-ethylhexyl) phosphate (diC2/6P), di(2-octyldodecyl) phosphate (diC8/12P), or di-n-dodecyl phosphate (diC12P), forming PBLG-b-PLL(diC4P), PBLG-b-PLL(diC2/6P), PBLG-b-PLL(diC8/12P), and PBLG-b-PLL(diC12P) complexes, respectively. The complexes contain PBLG α-helices of fixed diameter and PLL-surfactant complexes adopting either α-helices of tunable diameters or β-sheets. For PBLG-b-PLL(diC4P), that is, using a surfactant with short n-butyl tails, both blocks were α-helical, of roughly equal diameter and thus with minor packing frustrations, leading to alternating PBLG and PLL(diC4P) smectic layers of approximately perpendicular alignment of both types of α-helices. Surfactants with longer and branched alkyl tails lead to an increased diameter of the PLL-surfactant α-helices. Smectic alternating PBLG and PLL(diC2/6P) layers involve larger packing frustration, which leads to poor overall order and suggests an arrangement of tilted PBLG α-helices. In PBLG-b-PLL(diC8/12P), the PLL(diC8/12P) α-helices are even larger and the overall structure is poor. Using a surfactant with two linear n-dodecyl tails leads to well-ordered β-sheet domains of PLL(diC12P), consisting of alternating PLL and alkyl chain layers. This dominates the whole assembly, and at the block copolypeptide length scale, the PBLG α-helices do not show internal order and have poor organization. Packing frustration becomes an important aspect to design block copolypeptide assemblies, even if frustration could be relieved by conformational imperfections. The results suggest pathways to control hierarchical liquid-crystalline assemblies by competing interactions and by controlling molecular packing frustrations. © 2012 American Chemical Society.
Publication year:
2012
Authors:
Johannes S. Haataja
Nikolay Houbenov
Hermis Iatrou
Nikos Hadjichristidis
Anastasis Karatzas
Charl F. J. Faul
Patrice Rannou
Olli Ikkala
Journal:
Biomacromolecules
Publisher:
American Chemical Society (ACS)
Volume:
13
Number:
11
Pages:
3572--3580
Keywords:
Alkyl chain; Alternating layers; Amino residue; Block co-polypeptide; Design blocks; Di(2-ethylhexyl)phosphate; L-glutamate; l-Lysine; Length scale; Molecular packings; Polymeric scaffold; Rod-coil; Smectic layers, Amino acids; Polypeptides, Surface active agents, di n butyl phosphate; di n dodecyl phosphate; di(2 ethylhexyl)phosphate; di(2 octyldodecyl)phosphate; phosphate; poly(gamma benzyl levo glutamate) block poly(levo lysine); polypeptide; silicon dioxide; surfactant; tissue scaffold; unclassified drug, alpha helix; article; beta sheet; chemical structure; conformational transition; crystal; liquid; molecular size; priority journal; solid state, Liquid Crystals; Peptides; Polyglutamic Acid; Polylysine; Polymers; Protein Structure, Secondary; Surface-Active Agents; Water
Main subject category:
Science
Official URL (Publisher):
DOI:
10.1021/bm3010275
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