TY - JOUR
T1 - Modulating the pro-apoptotic activity of cytochrome c at a biomimetic electrified interface
AU - Gamero-Quijano, Alonso
AU - Bhattacharya, Shayon
AU - Cazade, Pierre André
AU - Molina-Osorio, Andrés F.
AU - Beecher, Cillian
AU - Djeghader, Ahmed
AU - Soulimane, Tewfik
AU - Dossot, Manuel
AU - Thompson, Damien
AU - Herzog, Grégoire
AU - Scanlon, Micheál D.
N1 - Publisher Copyright:
Copyright © 2021 The Authors, some rights reserved;
PY - 2021/11
Y1 - 2021/11
N2 - Programmed cell death via apoptosis is a natural defence against excessive cell division, crucial for fetal development to maintenance of homeostasis and elimination of precancerous and senescent cells. Here, we demonstrate an electrified liquid biointerface that replicates the molecular machinery of the inner mitochondrial membrane at the onset of apoptosis. By mimicking in vivo cytochrome c (Cyt c) interactions with cell membranes, our platform allows us to modulate the conformational plasticity of the protein by simply varying the electrochemical environment at an aqueous-organic interface. We observe interfacial electron transfer between an organic electron donor decamethylferrocene and O2, electrocatalyzed by Cyt c. This interfacial reaction requires partial Cyt c unfolding, mimicking Cyt c in vivo peroxidase activity. As proof of concept, we use our electrified liquid biointerface to identify drug molecules, such as bifonazole, that can potentially down-regulate Cyt c and protect against uncontrolled neuronal cell death in neurodegenerative disorders.
AB - Programmed cell death via apoptosis is a natural defence against excessive cell division, crucial for fetal development to maintenance of homeostasis and elimination of precancerous and senescent cells. Here, we demonstrate an electrified liquid biointerface that replicates the molecular machinery of the inner mitochondrial membrane at the onset of apoptosis. By mimicking in vivo cytochrome c (Cyt c) interactions with cell membranes, our platform allows us to modulate the conformational plasticity of the protein by simply varying the electrochemical environment at an aqueous-organic interface. We observe interfacial electron transfer between an organic electron donor decamethylferrocene and O2, electrocatalyzed by Cyt c. This interfacial reaction requires partial Cyt c unfolding, mimicking Cyt c in vivo peroxidase activity. As proof of concept, we use our electrified liquid biointerface to identify drug molecules, such as bifonazole, that can potentially down-regulate Cyt c and protect against uncontrolled neuronal cell death in neurodegenerative disorders.
UR - http://www.scopus.com/inward/record.url?scp=85118634314&partnerID=8YFLogxK
U2 - 10.1126/sciadv.abg4119
DO - 10.1126/sciadv.abg4119
M3 - Article
C2 - 34739310
AN - SCOPUS:85118634314
SN - 2375-2548
VL - 7
SP - eabg4119
JO - Science Advances
JF - Science Advances
IS - 45
M1 - eabg4119
ER -