<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Jin H</submitter><pubmed_abstract>Despite recent advances in the assembly of organic nanotubes, conferral of sequence-defined engineering and dynamic response characteristics to the tubules remains a challenge. Here we report a new family of highly designable and dynamic nanotubes assembled from sequence-defined peptoids through a unique "rolling-up and closure of nanosheet" mechanism. During the assembly process, amorphous spherical particles of amphiphilic peptoid oligomers crystallize to form well-defined nanosheets before folding to form single-walled nanotubes. These nanotubes undergo a pH-triggered, reversible contraction-expansion motion. By varying the number of hydrophobic residues of peptoids, we demonstrate tuning of nanotube wall thickness, diameter, and mechanical properties. Atomic force microscopy-based mechanical measurements show peptoid nanotubes are highly stiff (Young's Modulus ~13-17 GPa). We further demonstrate the precise incorporation of functional groups within nanotubes and their applications in water decontamination and cellular adhesion and uptake. These nanotubes provide a robust platform for developing biomimetic materials tailored to specific applications.</pubmed_abstract><journal>Nature communications</journal><pagination>270</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5773689</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Designable and dynamic single-walled stiff nanotubes assembled from sequence-defined peptoids.</pubmed_title><pmcid>PMC5773689</pmcid><pubmed_authors>Liao Z</pubmed_authors><pubmed_authors>Chen CL</pubmed_authors><pubmed_authors>Ding YH</pubmed_authors><pubmed_authors>Newcomb CJ</pubmed_authors><pubmed_authors>Lin Y</pubmed_authors><pubmed_authors>Wang M</pubmed_authors><pubmed_authors>Jin H</pubmed_authors><pubmed_authors>Li Z</pubmed_authors><pubmed_authors>Jian T</pubmed_authors><pubmed_authors>Mu P</pubmed_authors><pubmed_authors>Tang XQ</pubmed_authors><pubmed_authors>Song Y</pubmed_authors><pubmed_authors>Wu X</pubmed_authors><pubmed_authors>Yan F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Designable and dynamic single-walled stiff nanotubes assembled from sequence-defined peptoids.</name><description>Despite recent advances in the assembly of organic nanotubes, conferral of sequence-defined engineering and dynamic response characteristics to the tubules remains a challenge. Here we report a new family of highly designable and dynamic nanotubes assembled from sequence-defined peptoids through a unique "rolling-up and closure of nanosheet" mechanism. During the assembly process, amorphous spherical particles of amphiphilic peptoid oligomers crystallize to form well-defined nanosheets before folding to form single-walled nanotubes. These nanotubes undergo a pH-triggered, reversible contraction-expansion motion. By varying the number of hydrophobic residues of peptoids, we demonstrate tuning of nanotube wall thickness, diameter, and mechanical properties. Atomic force microscopy-based mechanical measurements show peptoid nanotubes are highly stiff (Young's Modulus ~13-17 GPa). We further demonstrate the precise incorporation of functional groups within nanotubes and their applications in water decontamination and cellular adhesion and uptake. These nanotubes provide a robust platform for developing biomimetic materials tailored to specific applications.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jan</publication><modification>2025-04-04T11:30:56.802Z</modification><creation>2019-03-26T22:58:21Z</creation></dates><accession>S-EPMC5773689</accession><cross_references><pubmed>29348551</pubmed><doi>10.1038/s41467-017-02059-1</doi></cross_references></HashMap>