<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Sgolastra F</submitter><funding>NSF</funding><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>131-136</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5568762</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>254</volume><pubmed_abstract>The impermeability of the plasma membrane towards large, hydrophilic biomolecules is a major obstacle in their use and development against intracellular targets. To overcome such limitations, protein transduction domains (PTDs) have been used as protein carriers, however they often require covalent fusion to the protein for efficient delivery. In an effort to develop more efficient and versatile biological vehicles, a series of PTD-inspired polyoxanorbornene-based synthetic mimics with identical chemical compositions but different hydrophobic/hydrophilic segregation were used to investigate the role of sequence segregation on protein binding and uptake into Jurkat T cells and HEK293Ts. This series was composed of a strongly segregated block copolymer, an intermediately segregated gradient </pubmed_abstract><journal>Journal of controlled release : official journal of the Controlled Release Society</journal><pubmed_title>Sequence segregation improves non-covalent protein delivery.</pubmed_title><pmcid>PMC5568762</pmcid><funding_grant_id>P01 CA166009</funding_grant_id><funding_grant_id>CHE-0910963</funding_grant_id><funding_grant_id>T32 GM008515</funding_grant_id><pubmed_authors>deRonde BM</pubmed_authors><pubmed_authors>Ilker Ozay E</pubmed_authors><pubmed_authors>Backlund CM</pubmed_authors><pubmed_authors>Minter LM</pubmed_authors><pubmed_authors>Sgolastra F</pubmed_authors><pubmed_authors>Tew GN</pubmed_authors></additional><is_claimable>false</is_claimable><name>Sequence segregation improves non-covalent protein delivery.</name><description>The impermeability of the plasma membrane towards large, hydrophilic biomolecules is a major obstacle in their use and development against intracellular targets. To overcome such limitations, protein transduction domains (PTDs) have been used as protein carriers, however they often require covalent fusion to the protein for efficient delivery. In an effort to develop more efficient and versatile biological vehicles, a series of PTD-inspired polyoxanorbornene-based synthetic mimics with identical chemical compositions but different hydrophobic/hydrophilic segregation were used to investigate the role of sequence segregation on protein binding and uptake into Jurkat T cells and HEK293Ts. This series was composed of a strongly segregated block copolymer, an intermediately segregated gradient </description><dates><release>2017-01-01T00:00:00Z</release><publication>2017 May</publication><modification>2025-04-21T14:09:48.442Z</modification><creation>2019-03-27T02:54:20Z</creation></dates><accession>S-EPMC5568762</accession><cross_references><pubmed>28363520</pubmed><doi>10.1016/j.jconrel.2017.03.387</doi></cross_references></HashMap>