TY - JOUR
T1 - On-Demand Electrical Switching of Antibody-Antigen Binding on Surfaces
AU - Gomes, Bárbara
AU - Cantini, Eleonora
AU - Tommasone, Stefano
AU - Gibson, Joshua
AU - Wang, Xingyong
AU - Zhu, Qiang
AU - McGettrick, James
AU - Watson, Trystan
AU - Preece, Jon
AU - Kirkman-Brown, Jackson
AU - Publicover, Stephen
AU - Mendes, Paula
PY - 2018/9/17
Y1 - 2018/9/17
N2 - The development of stimuli-responsive interfaces between synthetic materials and biological systems is providing the unprecedented ability to modulate biomolecular interactions for a diverse range of biotechnological and biomedical applications. Antibody–antigen binding interactions are at the heart of many biosensing platforms, but no attempts have been made yet to control antibody–antigen binding in an on-demand fashion. Herein, a molecular surface was designed and developed that utilizes an electric potential to drive a conformational change in surface bound peptide moiety, to give on-demand control over antigen–antibody interactions on sensor chips. The molecularly engineered surfaces allow for propagation of conformational changes from the molecular switching unit to a distal progesterone antigen, resulting in promotion (ON state) or inhibition (OFF state) of progesterone antibody binding. The approach presented here can be generally applicable to other antigen–antibody systems and meets the technological needs for in situ long-term assessment of biological processes and disease monitoring on-demand.
AB - The development of stimuli-responsive interfaces between synthetic materials and biological systems is providing the unprecedented ability to modulate biomolecular interactions for a diverse range of biotechnological and biomedical applications. Antibody–antigen binding interactions are at the heart of many biosensing platforms, but no attempts have been made yet to control antibody–antigen binding in an on-demand fashion. Herein, a molecular surface was designed and developed that utilizes an electric potential to drive a conformational change in surface bound peptide moiety, to give on-demand control over antigen–antibody interactions on sensor chips. The molecularly engineered surfaces allow for propagation of conformational changes from the molecular switching unit to a distal progesterone antigen, resulting in promotion (ON state) or inhibition (OFF state) of progesterone antibody binding. The approach presented here can be generally applicable to other antigen–antibody systems and meets the technological needs for in situ long-term assessment of biological processes and disease monitoring on-demand.
U2 - 10.1021/acsabm.8b00201
DO - 10.1021/acsabm.8b00201
M3 - Article
SN - 2576-6422
VL - 1
SP - 738
EP - 747
JO - ACS Applied Bio Materials
JF - ACS Applied Bio Materials
IS - 3
ER -