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Shape-Shifting Peptide Nanomaterials: Surface Asymmetry Enables pH-Dependent Formation and Interconversion of Collagen Tubes and Sheets
JournalArticle (Originalarbeit in einer wissenschaftlichen Zeitschrift)
 
ID 4612414
Author(s) Merg, Andrea D.; Touponse, Gavin; van Genderen, Eric; Blum, Thorsten B.; Zuo, Xiaobing; Bazrafshan, Alisina; Siaw, Hew Ming Helen; McCanna, Arthur; Dyer, R. Brian; Salaita, Khalid; Abrahams, Jan Pieter; Conticello, Vincent P.
Author(s) at UniBasel Abrahams, Jan Pieter
Year 2020
Title Shape-Shifting Peptide Nanomaterials: Surface Asymmetry Enables pH-Dependent Formation and Interconversion of Collagen Tubes and Sheets
Journal Journal of the American Chemical Society
Volume 142
Number 47
Pages / Article-Number 19956-19968
Abstract The fabrication of dynamic, transformable biomaterials that respond to environmental cues represents a significant step forward in the development of synthetic materials that rival their highly functional, natural counterparts. Here, we describe the design and synthesis of crystalline supramolecular architectures from charge-complementary heteromeric pairs of collagen-mimetic peptides (CMPs). Under appropriate conditions, CMP pairs spontaneously assemble into either 1D ultraporous (pore diameter >100 nm) tubes or 2D bilayer nanosheets due to the structural asymmetry that arises from heteromeric self-association. Crystalline collagen tubes represent a heretofore unobserved morphology of this common biomaterial. In-depth structural characterization from a suite of biophysical methods, including TEM, AFM, high-resolution cryo-EM, and SAXS/WAXS measurements, reveals that the sheet and tube assemblies possess a similar underlying lattice structure. The experimental evidence suggests that the tubular structures are a consequence of the self-scrolling of incipient 2D layers of collagen triple helices and that the scrolling direction determines the formation of two distinct structural isoforms. Furthermore, we show that nanosheets and tubes can spontaneously interconvert through manipulation of the assembly pH and systematic adjustment of the CMP sequence. Altogether, we establish initial guidelines for the construction of dynamically responsive 1D and 2D assemblies that undergo a structurally programmed morphological transition.
Publisher American Chemical Society
ISSN/ISBN 0002-7863 ; 1520-5126
edoc-URL https://edoc.unibas.ch/80635/
Full Text on edoc No
Digital Object Identifier DOI 10.1021/jacs.0c08174
PubMed ID http://www.ncbi.nlm.nih.gov/pubmed/33170675
Document type (ISI) Journal Article
 
   

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