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Direct Immobilization of Engineered Nanobodies on Gold Sensors
Author(s) -
Bárbara Simões,
Wanda Guedens,
Charlie Keene,
Karina Kubiak-Ossowska,
Paul A. Mulheran,
Anna M. Kotowska,
David J. Scurr,
Morgan R. Alexander,
Alexis Broisat,
Steven D. Johnson,
Serge Muyldermans,
Nick Devoogdt,
Peter Adriaensens,
Paula M. Mendes
Publication year - 2021
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.1c02280
Subject(s) - surface plasmon resonance , single domain antibody , materials science , nanotechnology , circular dichroism , biosensor , nanoparticle , chemistry , antibody , crystallography , immunology , biology
Single-domain antibodies, known as nanobodies, have great potential as biorecognition elements for sensors because of their small size, affinity, specificity, and robustness. However, facile and efficient methods of nanobody immobilization are sought that retain their maximum functionality. Herein, we describe the direct immobilization of nanobodies on gold sensors by exploiting a modified cysteine strategically positioned at the C-terminal end of the nanobody. The experimental data based on secondary ion mass spectrometry, circular dichroism, and surface plasmon resonance, taken together with a detailed computational work (molecular dynamics simulations), support the formation of stable and well-oriented nanobody monolayers. Furthermore, the nanobody structure and activity is preserved, wherein the nanobody is immobilized at a high density (approximately 1 nanobody per 13 nm 2 ). The strategy for the spontaneous nanobody self-assembly is simple and effective and possesses exceptional potential to be used in numerous sensing platforms, ranging from clinical diagnosis to environmental monitoring.

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