表面等离子共振
单域抗体
材料科学
纳米技术
生物传感器
圆二色性
纳米颗粒
化学
抗体
结晶学
生物
免疫学
作者
Bárbara Simões,Wanda Guedens,Charlie Keene,Karina Kubiak-Ossowska,Paul A. Mulheran,Anna M. Kotowska,David J. Scurr,Morgan R. Alexander,Alexis Broisat,Steven Johnson,Serge Muyldermans,Nick Devoogdt,Peter Adriaensens,Paula M. Mendes
标识
DOI:10.1021/acsami.1c02280
摘要
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.
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