<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Mei KC</submitter><funding>Generalitat de Catalunya</funding><funding>MINECO</funding><funding>China Scholarship Council</funding><funding>Severo Ochoa programme</funding><funding>Graduate School International Research</funding><funding>Ministerio de Economía y Competitividad</funding><funding>Biotechnology and Biological Sciences Research Council</funding><funding>The British Council</funding><funding>CERCA</funding><funding>Engineering and Physical Sciences Research Council</funding><pubmed_abstract>Hard corona (HC) protein, i.e., the environmental proteins of the biological medium that are bound to a nanosurface, is known to affect the biological fate of a nanomedicine. Due to the size, curvature, and specific surface area (SSA) 3-factor interactions inherited in the traditional 3D nanoparticle, HC-dependent bio-nano interactions are often poorly probed and interpreted. Here, the first HC-by-design case study in 2D is demonstrated that sequentially and linearly changes the HC quantity using functionalized graphene oxide (GO) nanosheets. The HC quantity and HC quality are analyzed using NanoDrop and label-free liquid chromatography-mass spectrometry (LC-MS) followed by principal component analysis (PCA). Cellular responses (uptake and cytotoxicity in J774 cell model) are compared usin</pubmed_abstract><journal>Advanced materials (Deerfield Beach, Fla.)</journal><pagination>e1802732</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6952277</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Protein-Corona-by-Design in 2D: A Reliable Platform to Decode Bio-Nano Interactions for the Next-Generation Quality-by-Design Nanomedicines.</pubmed_title><pmcid>PMC6952277</pmcid><funding_grant_id>337313</funding_grant_id><funding_grant_id>EP/N013506/1</funding_grant_id><funding_grant_id>BB/J008656/1</funding_grant_id><funding_grant_id>SEV-2013-0295</funding_grant_id><pubmed_authors>Ghazaryan A</pubmed_authors><pubmed_authors>Li Y</pubmed_authors><pubmed_authors>Mei KC</pubmed_authors><pubmed_authors>Mailander V</pubmed_authors><pubmed_authors>Ballesteros B</pubmed_authors><pubmed_authors>Summers HD</pubmed_authors><pubmed_authors>Hider RC</pubmed_authors><pubmed_authors>Al-Jamal KT</pubmed_authors><pubmed_authors>Teoh EZ</pubmed_authors><pubmed_authors>Piasecka J</pubmed_authors><pubmed_authors>Walters A</pubmed_authors></additional><is_claimable>false</is_claimable><name>Protein-Corona-by-Design in 2D: A Reliable Platform to Decode Bio-Nano Interactions for the Next-Generation Quality-by-Design Nanomedicines.</name><description>Hard corona (HC) protein, i.e., the environmental proteins of the biological medium that are bound to a nanosurface, is known to affect the biological fate of a nanomedicine. Due to the size, curvature, and specific surface area (SSA) 3-factor interactions inherited in the traditional 3D nanoparticle, HC-dependent bio-nano interactions are often poorly probed and interpreted. Here, the first HC-by-design case study in 2D is demonstrated that sequentially and linearly changes the HC quantity using functionalized graphene oxide (GO) nanosheets. The HC quantity and HC quality are analyzed using NanoDrop and label-free liquid chromatography-mass spectrometry (LC-MS) followed by principal component analysis (PCA). Cellular responses (uptake and cytotoxicity in J774 cell model) are compared usin</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2025-04-19T03:37:26.197Z</modification><creation>2020-05-22T07:24:32Z</creation></dates><accession>S-EPMC6952277</accession><cross_references><pubmed>30144166</pubmed><doi>10.1002/adma.201802732</doi></cross_references></HashMap>