<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Negron LM</submitter><funding>National Institute of General Medical Sciences</funding><funding>NIGMS NIH HHS</funding><pagination>2283-90</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4896646</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>32(10)</volume><pubmed_abstract>Nanoflowers (NFs) are flowered-shaped particles with overall sizes or features in the nanoscale. Beyond their pleasing aesthetics, NFs have found a number of applications ranging from catalysis, to sensing, to drug delivery. Compared to inorganic based NFs, their organic and hybrid counterparts are relatively underdeveloped mostly because of the lack of a reliable and versatile method for their construction. We report here a method for constructing NFs from a wide variety of biologically relevant molecules (guests), ranging from small molecules, like doxorubicin, to biomacromolecules, like various proteins and plasmid DNA. The method relies on the encapsulation of the guests within a hierarchically structured particle made from supramolecular G-quadruplexes. The size and overall flexibility of the guests dictate the broad morphological features of the resulting NFs, specifically, small and rigid guests favor the formation of NFs with spiky petals, while large and/or flexible guests promote NFs with wide petals. The results from experiments using confocal fluorescence microscopy, and scanning electron microscopy provides the basis for the proposed mechanism for the NF formation.</pubmed_abstract><journal>Langmuir : the ACS journal of surfaces and colloids</journal><pubmed_title>Organic Nanoflowers from a Wide Variety of Molecules Templated by a Hierarchical Supramolecular Scaffold.</pubmed_title><pmcid>PMC4896646</pmcid><funding_grant_id>P20 GM 103642</funding_grant_id><funding_grant_id>R25 GM061151</funding_grant_id><funding_grant_id>P20 GM103642</funding_grant_id><funding_grant_id>P20GM 103642</funding_grant_id><funding_grant_id>SC1 GM093994</funding_grant_id><funding_grant_id>5SC1GM093994</funding_grant_id><funding_grant_id>5R25GM061151</funding_grant_id><pubmed_authors>Dieppa-Matos D</pubmed_authors><pubmed_authors>Madera-Soto B</pubmed_authors><pubmed_authors>Ortiz-Quiles EO</pubmed_authors><pubmed_authors>Negron LM</pubmed_authors><pubmed_authors>Diaz TL</pubmed_authors><pubmed_authors>Rivera JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>Organic Nanoflowers from a Wide Variety of Molecules Templated by a Hierarchical Supramolecular Scaffold.</name><description>Nanoflowers (NFs) are flowered-shaped particles with overall sizes or features in the nanoscale. Beyond their pleasing aesthetics, NFs have found a number of applications ranging from catalysis, to sensing, to drug delivery. Compared to inorganic based NFs, their organic and hybrid counterparts are relatively underdeveloped mostly because of the lack of a reliable and versatile method for their construction. We report here a method for constructing NFs from a wide variety of biologically relevant molecules (guests), ranging from small molecules, like doxorubicin, to biomacromolecules, like various proteins and plasmid DNA. The method relies on the encapsulation of the guests within a hierarchically structured particle made from supramolecular G-quadruplexes. The size and overall flexibility of the guests dictate the broad morphological features of the resulting NFs, specifically, small and rigid guests favor the formation of NFs with spiky petals, while large and/or flexible guests promote NFs with wide petals. The results from experiments using confocal fluorescence microscopy, and scanning electron microscopy provides the basis for the proposed mechanism for the NF formation.</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2025-04-04T02:03:59.574Z</modification><creation>2019-03-27T02:15:31Z</creation></dates><accession>S-EPMC4896646</accession><cross_references><pubmed>26901110</pubmed><doi>10.1021/acs.langmuir.5b03946</doi></cross_references></HashMap>