<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Lebegue E</submitter><funding>H2020 Marie Sklodowska-Curie Actions</funding><funding>Minist?re de l&amp;apos;Education Nationale, de l&amp;apos;Enseignement Superieur et de la Recherche</funding><funding>Minist?re de l?Europe et des Affaires ?trang?res</funding><funding>FCT - Funda??o para a Ci?ncia e a Tecnologia</funding><pagination>9035-9042</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6644398</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>3(8)</volume><pubmed_abstract>The electrochemical systems of both grafted catechol as a pH-responsive electrophore and immobilized cytochrome &lt;i>c&lt;/i> as a model redox protein are detected by cyclic voltammetry at an optimized lipid deposit-modified glassy carbon electrode. The catechol covalent grafting is successfully performed by the one-pot/three-step electrochemical reduction of 3,4-dihydroxybenzenediazonium salts generated in situ from 4-nitrocatechol. The resulting glassy carbon electrode electrochemically modified by grafted catechol species is evaluated as an efficient electrochemical pH sensor. The optimized molar ratio for the lipid deposit, promoting cytochrome &lt;i>c&lt;/i> electrochemical activity in solution onto glassy carbon electrode, is reached for the lipid mixture composed of 75% 1,2-dioleoyl-&lt;i>sn&lt;/i>-glycero-3-phosphocholine and 25% cardiolipin. Cytochrome &lt;i>c&lt;/i> immobilization into the optimized supported lipid deposit is efficiently achieved by cyclic voltammetry (10 cycles) recorded at the modified glassy carbon electrode in a cytochrome &lt;i>c&lt;/i> solution. The pH-dependent redox response of the grafted catechol and that of the immobilized cytochrome &lt;i>c&lt;/i> are finally detected at the same lipid-modified glassy carbon electrode without alteration of their structure and electrochemical properties in the pH range 5-9.</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Electrochemical Detection of pH-Responsive Grafted Catechol and Immobilized Cytochrome &lt;i>c&lt;/i> onto Lipid Deposit-Modified Glassy Carbon Surface.</pubmed_title><pmcid>PMC6644398</pmcid><funding_grant_id>40814ZE</funding_grant_id><funding_grant_id>745689</funding_grant_id><pubmed_authors>Louro RO</pubmed_authors><pubmed_authors>Lebegue E</pubmed_authors><pubmed_authors>Barriere F</pubmed_authors></additional><is_claimable>false</is_claimable><name>Electrochemical Detection of pH-Responsive Grafted Catechol and Immobilized Cytochrome &lt;i>c&lt;/i> onto Lipid Deposit-Modified Glassy Carbon Surface.</name><description>The electrochemical systems of both grafted catechol as a pH-responsive electrophore and immobilized cytochrome &lt;i>c&lt;/i> as a model redox protein are detected by cyclic voltammetry at an optimized lipid deposit-modified glassy carbon electrode. The catechol covalent grafting is successfully performed by the one-pot/three-step electrochemical reduction of 3,4-dihydroxybenzenediazonium salts generated in situ from 4-nitrocatechol. The resulting glassy carbon electrode electrochemically modified by grafted catechol species is evaluated as an efficient electrochemical pH sensor. The optimized molar ratio for the lipid deposit, promoting cytochrome &lt;i>c&lt;/i> electrochemical activity in solution onto glassy carbon electrode, is reached for the lipid mixture composed of 75% 1,2-dioleoyl-&lt;i>sn&lt;/i>-glycero-3-phosphocholine and 25% cardiolipin. Cytochrome &lt;i>c&lt;/i> immobilization into the optimized supported lipid deposit is efficiently achieved by cyclic voltammetry (10 cycles) recorded at the modified glassy carbon electrode in a cytochrome &lt;i>c&lt;/i> solution. The pH-dependent redox response of the grafted catechol and that of the immobilized cytochrome &lt;i>c&lt;/i> are finally detected at the same lipid-modified glassy carbon electrode without alteration of their structure and electrochemical properties in the pH range 5-9.</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Aug</publication><modification>2024-02-14T20:16:30.719Z</modification><creation>2019-08-31T07:03:49Z</creation></dates><accession>S-EPMC6644398</accession><cross_references><pubmed>31459037</pubmed><doi>10.1021/acsomega.8b01425</doi></cross_references></HashMap>