Cheng Zihe, Hall Stephen C L, Song Qiao, Perrier Sébastien
Department of Chemistry, University of Warwick, Coventry CV4 7AL, U.K.
ISIS Neutron and Muon Source, Rutherford Appleton Laboratory, Didcot OX11 0QX, U.K.
ACS Macro Lett. 2025 Mar 18;14(3):292-298. doi: 10.1021/acsmacrolett.4c00759. Epub 2025 Feb 20.
Supramolecular polymeric nanotubes based on the self-assembling cyclic peptide-polymer conjugates are a promising class of materials, showing great potential in various biological applications. Herein, we present a novel strategy to promote nanotube assembly through effectively shielding the cyclic peptides from water, via the introduction of varying hydrophobic groups. As determined by a combination of SANS, TEM, and SLS, hydrophobic interactions, π-π stacking, and multiple hydrogen bonding interactions cooperate in the self-assembly of the cyclic peptide-polymer conjugates, allowing for the construction of supramolecular nanotubes that are longer than expected in water. This approach offers an effective pathway toward the design of organic nanotubes of hundreds of nanometers in water.
基于自组装环肽-聚合物共轭物的超分子聚合物纳米管是一类很有前景的材料,在各种生物应用中显示出巨大潜力。在此,我们提出了一种新策略,通过引入不同的疏水基团有效地将环肽与水隔离,从而促进纳米管组装。通过小角中子散射(SANS)、透射电子显微镜(TEM)和静态光散射(SLS)相结合的方法确定,疏水相互作用、π-π堆积和多重氢键相互作用在环肽-聚合物共轭物的自组装过程中协同作用,使得能够构建出在水中比预期更长的超分子纳米管。这种方法为设计水中数百纳米的有机纳米管提供了一条有效途径。