High spatial resolution label-free detection of antigen–antibody binding on patterned surface by imaging ellipsometry

2011 ◽  
Vol 360 (2) ◽  
pp. 826-833 ◽  
Author(s):  
Meng-Jie Chang ◽  
Chao-Ran Pang ◽  
Jun Liu ◽  
Hua Bai ◽  
Jun Deng ◽  
...  
Micromachines ◽  
2021 ◽  
Vol 12 (4) ◽  
pp. 390
Author(s):  
Maryia Drobysh ◽  
Almira Ramanaviciene ◽  
Roman Viter ◽  
Arunas Ramanavicius

The coronavirus disease 2019 (COVID-19) outbreak caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) was proclaimed a global pandemic in March 2020. Reducing the dissemination rate, in particular by tracking the infected people and their contacts, is the main instrument against infection spreading. Therefore, the creation and implementation of fast, reliable and responsive methods suitable for the diagnosis of COVID-19 are required. These needs can be fulfilled using affinity sensors, which differ in applied detection methods and markers that are generating analytical signals. Recently, nucleic acid hybridization, antigen-antibody interaction, and change of reactive oxygen species (ROS) level are mostly used for the generation of analytical signals, which can be accurately measured by electrochemical, optical, surface plasmon resonance, field-effect transistors, and some other methods and transducers. Electrochemical biosensors are the most consistent with the general trend towards, acceleration, and simplification of the bioanalytical process. These biosensors mostly are based on the determination of antigen-antibody interaction and are robust, sensitive, accurate, and sometimes enable label-free detection of an analyte. Along with the specification of biosensors, we also provide a brief overview of generally used testing techniques, and the description of the structure, life cycle and immune host response to SARS-CoV-2, and some deeper details of analytical signal detection principles.


2007 ◽  
Vol 60 (9) ◽  
pp. 667 ◽  
Author(s):  
Irina Chamritski ◽  
Mark Clarkson ◽  
Jeff Franklin ◽  
Shi Wei Li

In the field of proteomics the quantification of the affinity of an antibody to its partners and the evaluation of its specific binding is an important issue. With an imaging ellipsometer the interaction of an antibody with immobilized antigens on a model microarray is observed in a time-resolved and label-free manner. Imaging ellipsometry was developed for real-time monitoring of the biomolecule interaction between an antigen in solution and an antibody immobilized on a silicon surface. Proteins were immobilized by the formation of carboxy-alkyl monolayers on silicon substrates, where a biotin-labelled antibody was immobilized by a biotin–streptavidin linkage. Anti-human IgG bound specifically to human antibody and protein A, similarly anti-goat IgG bound to goat antibody. No binding was observed between anti-rabbit IgG and goat antibody. All stages of the formation of the antigen–antibody complex were imaged by imaging ellipsometry. By monitoring changes in y, the mole fraction θ of the antigen–antibody binding was determined. Immunological reactions of two different antigen–antibody combinations were fitted by the Langmuir adsorption equation, and affinity constants for two reactions were calculated.


The Analyst ◽  
2014 ◽  
Vol 139 (4) ◽  
pp. 729-733 ◽  
Author(s):  
F. Palombo ◽  
M. Madami ◽  
N. Stone ◽  
D. Fioretto

Confocal Brillouin and Raman microscopies provide non-contact label-free mechanochemical mapping of epithelial tissue, Barrett's oesophagus at high spatial resolution.


2009 ◽  
Vol 2009 ◽  
pp. 1-12 ◽  
Author(s):  
Imen Hafaid ◽  
Asma Gallouz ◽  
Walid Mohamed Hassen ◽  
Adnane Abdelghani ◽  
Zina Sassi ◽  
...  

This work has explored the development of impedimetric immunosensors based on magnetic iron nanoparticles (IrNP) functionalized with streptavidin to which a biotinylated FAB part of the antibody has been bound using a biotin-streptavidin interaction. SPR analysis shows a deviation on the measured (angle) during antigen-antibody recognition whereas label free detection using by EIS allows us to monitor variation of polarization resistance. Before detection, layers were analyzed by FTIR and AFM. Compared to immobilization of antibody on bare gold surface using aminodecanethiol SAM, antibody immobilization on nanoparticles permitted to reach lower detection limit: 500 pg/ml instead of 1 ng/ml to in the case of EIS and 300 ng/ml instead of 4.5 μg/ml in the case of SPR. Thus, it permitted to improve the sensitivity: from 257.3 Ω⋅cm2⋅μg−1⋅mlto 1871 Ω⋅cm2⋅μg−1⋅mlin the case of EIS and from0.003°μg−1⋅mlto0.094°μg−1⋅mlin the case of SPR.


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