| Literature DB >> 33845569 |
Bárbara Simões1, Wanda J Guedens2, Charlie Keene1, Karina Kubiak-Ossowska3, Paul Mulheran4, Anna M Kotowska5, David J Scurr5, Morgan R Alexander5, Alexis Broisat6, Steven Johnson7, Serge Muyldermans8, Nick Devoogdt9, Peter Adriaensens2, Paula M Mendes1.
Abstract
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 nm2). 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.Entities:
Keywords: molecular dynamic simulations; nanobody; sensor; single-domain antibody; surface plasmon resonance
Year: 2021 PMID: 33845569 DOI: 10.1021/acsami.1c02280
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229