| Literature DB >> 31291499 |
Andrea D Merg1, Gavin Touponse1, Eric van Genderen2, Xiaobing Zuo3, Alisina Bazrafshan1, Thorsten Blum2, Spencer Hughes1, Khalid Salaita1, Jan Pieter Abrahams2,4,5, Vincent P Conticello1.
Abstract
The successful integration of 2D nanomaterials into functional devices hinges on developing fabrication methods that afford hierarchical control across length scales of the entire assembly. We demonstrate structural control over a class of crystalline 2D nanosheets assembled from collagen triple helices. By lengthening the triple helix unit through sequential additions of Pro-Hyp-Gly triads, we achieved sub-angstrom tuning over the 2D lattice. These subtle changes influence the overall nanosheet size, which can be adjusted across the mesoscale size regime. The internal structure was observed by cryo-TEM with direct electron detection, which provides real-space high-resolution images, in which individual triple helices comprising the lattice can be clearly discerned. These results establish a general strategy for tuning the structural hierarchy of 2D nanomaterials that employ rigid, cylindrical structural units.Keywords: biomaterials; collagen; nanosheets; peptides; self-assembly
Year: 2019 PMID: 31291499 DOI: 10.1002/anie.201906214
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336