<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(35)</volume><submitter>Posey ND</submitter><funding>National Institute of Standards and Technology</funding><pubmed_abstract>A synthetic strategy yielded polyelectrolytes and polyampholytes with tunable net charge for complexation and protein binding. Organocatalytic ring-opening polymerizations yielded aliphatic polycarbonates that were functionalized with both carboxylate and ammonium side chains in a post-polymerization, radical-mediated thiol-ene reaction. Incorporating net charge into the polymer architecture altered the chain dimensions in phosphate buffered solution in a manner consistent with self-complexation and complexation behavior with model proteins. A net cationic polyampholyte with 5% of carboxylate side chains formed large clusters rather than small complexes with bovine serum albumin, while 50% carboxylate polyampholyte was insoluble. Overall, the aliphatic polycarbonates with varying net charge exhibited different macrophase solution behaviors when mixed with protein, where self-complexation appears to compete with protein binding and larger-scale complexation.</pubmed_abstract><journal>ACS omega</journal><pagination>22589-22602</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8427630</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tuning Net Charge in Aliphatic Polycarbonates Alters Solubility and Protein Complexation Behavior.</pubmed_title><pmcid>PMC8427630</pmcid><pubmed_authors>Danischewski J</pubmed_authors><pubmed_authors>Fagan JA</pubmed_authors><pubmed_authors>Prabhu VM</pubmed_authors><pubmed_authors>Ma Y</pubmed_authors><pubmed_authors>Posey ND</pubmed_authors><pubmed_authors>Lueckheide M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tuning Net Charge in Aliphatic Polycarbonates Alters Solubility and Protein Complexation Behavior.</name><description>A synthetic strategy yielded polyelectrolytes and polyampholytes with tunable net charge for complexation and protein binding. Organocatalytic ring-opening polymerizations yielded aliphatic polycarbonates that were functionalized with both carboxylate and ammonium side chains in a post-polymerization, radical-mediated thiol-ene reaction. Incorporating net charge into the polymer architecture altered the chain dimensions in phosphate buffered solution in a manner consistent with self-complexation and complexation behavior with model proteins. A net cationic polyampholyte with 5% of carboxylate side chains formed large clusters rather than small complexes with bovine serum albumin, while 50% carboxylate polyampholyte was insoluble. Overall, the aliphatic polycarbonates with varying net charge exhibited different macrophase solution behaviors when mixed with protein, where self-complexation appears to compete with protein binding and larger-scale complexation.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Sep</publication><modification>2024-02-15T03:50:22.245Z</modification><creation>2022-02-11T10:49:10.175Z</creation></dates><accession>S-EPMC8427630</accession><cross_references><pubmed>34514231</pubmed><doi>10.1021/acsomega.1c02523</doi></cross_references></HashMap>