<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>6(2)</volume><submitter>Tricase A</submitter><pubmed_abstract>Herein, we describe a novel method for producing cadmium-selenide nanoparticles (CdSe NPs) with controlled size using apoferritin as a bionanoreactor triggered by local pH change at the electrode/solution interface. Apoferritin is known for its reversible self-assembly at alkaline pH. The pH change is induced electrochemically by reducing O&lt;sub>2&lt;/sub> through the application of sufficiently negative voltages and bioelectrochemically through O&lt;sub>2&lt;/sub> reduction catalyzed by laccase, co-immobilized with apoferritin on the electrode surface. Specifically, a Ti electrode is modified with (3-aminopropyl)triethoxysilane, followed by glutaraldehyde cross-linking (1.5% v/v in H&lt;sub>2&lt;/sub>O) of apoferritin (as the bionanoreactor) and laccase (as the local pH change triggering system). This pr</pubmed_abstract><journal>Nanoscale advances</journal><pagination>516-523</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10790968</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Bioelectrochemically triggered apoferritin-based bionanoreactors: synthesis of CdSe nanoparticles and monitoring with leaky waveguides.</pubmed_title><pmcid>PMC10790968</pmcid><pubmed_authors>Gupta R</pubmed_authors><pubmed_authors>Bollella P</pubmed_authors><pubmed_authors>Marchiano V</pubmed_authors><pubmed_authors>Torsi L</pubmed_authors><pubmed_authors>Tricase A</pubmed_authors><pubmed_authors>Alhenaki B</pubmed_authors></additional><is_claimable>false</is_claimable><name>Bioelectrochemically triggered apoferritin-based bionanoreactors: synthesis of CdSe nanoparticles and monitoring with leaky waveguides.</name><description>Herein, we describe a novel method for producing cadmium-selenide nanoparticles (CdSe NPs) with controlled size using apoferritin as a bionanoreactor triggered by local pH change at the electrode/solution interface. Apoferritin is known for its reversible self-assembly at alkaline pH. The pH change is induced electrochemically by reducing O&lt;sub>2&lt;/sub> through the application of sufficiently negative voltages and bioelectrochemically through O&lt;sub>2&lt;/sub> reduction catalyzed by laccase, co-immobilized with apoferritin on the electrode surface. Specifically, a Ti electrode is modified with (3-aminopropyl)triethoxysilane, followed by glutaraldehyde cross-linking (1.5% v/v in H&lt;sub>2&lt;/sub>O) of apoferritin (as the bionanoreactor) and laccase (as the local pH change triggering system). This pr</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jan</publication><modification>2025-04-03T22:42:54.287Z</modification><creation>2024-10-16T09:04:11.601Z</creation></dates><accession>S-EPMC10790968</accession><cross_references><pubmed>38235094</pubmed><doi>10.1039/d3na01046e</doi></cross_references></HashMap>