SPR biosensor chip based on mannan isolated from Candida dubliniensis yeasts applied in immunization effectiveness testing

2021 ◽  
pp. 130883
Author(s):  
Jaroslav Katrlík ◽  
Alena Holazová ◽  
Izabela Medovarská ◽  
Ivana Seilerová ◽  
Peter Gemeiner ◽  
...  
2014 ◽  
Vol 9 (1) ◽  
Author(s):  
Nan-Fu Chiu ◽  
Teng-Yi Huang ◽  
Hsin-Chih Lai ◽  
Kou-Chen Liu

2007 ◽  
Vol 53 (2) ◽  
pp. 334-341 ◽  
Author(s):  
Alexander Buhl ◽  
Jochen H Metzger ◽  
Niels H H Heegaard ◽  
Philipp von Landenberg ◽  
Martin Fleck ◽  
...  

Abstract Background: Patients with systemic lupus erythematosus (SLE) develop a wide variety of serologic manifestations, including double-stranded DNA autoantibodies (anti-dsDNA). The determination of the potentially pathogenic autoantibodies is diagnostically relevant. Methods: We developed a novel surface plasmon resonance (SPR) biosensor chip for studies of dsDNA and anti-dsDNA binding. A synthetic oligonucleotide was coupled to biotinylated human transferrin, hybridized with the complementary antistrand, and ligated with a human recombinant dsDNA fragment 233 bp in length. After surface immobilization of this antigenic construct, diluted sera from SLE patients and healthy donors were analyzed with the resulting SPR biosensor system. Results: This SPR biosensor allowed specific detection of anti-dsDNA. In pilot experiments, sera from SLE patients were distinguished from control sera. We also confirmed the specificity of this biosensor by supplementing anti-dsDNA–positive sera with salmon sperm DNA, which blocked the surface binding of anti-dsDNA in a concentration-dependent manner. Conclusions: An SPR biosensor monitors interactions in real time under homogeneous conditions, providing information about binding kinetics and affinities. Its applicability critically depends on the design of the solid-state surface of the sensor chips. Covalently immobilizing dsDNA as the antigen to the surface in a flow-through cell assured maximal stability for multiple serum injections and regeneration cycles. This technique, which adds a new analytic quality to existing methods, may be beneficial in the diagnosis and clinical monitoring of SLE.


2013 ◽  
Vol 186 ◽  
pp. 423-430 ◽  
Author(s):  
T.F. McGrath ◽  
J. Buijs ◽  
A.C. Huet ◽  
P. Delahaut ◽  
C.T. Elliott ◽  
...  

2008 ◽  
Vol 148 (1-2) ◽  
pp. 120-124 ◽  
Author(s):  
Sang-Woo Kim ◽  
Min-Gon Kim ◽  
Jinju Kim ◽  
Hyun-Sook Lee ◽  
Hyeon-Su Ro

Biosensors ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 80
Author(s):  
Khaled Alsabbagh ◽  
Tim Hornung ◽  
Achim Voigt ◽  
Sahba Sadir ◽  
Taleieh Rajabi ◽  
...  

A microfluidic chip for electrochemical impedance spectroscopy (EIS) is presented as bio-sensor for label-free detection of proteins by using the example of cardiac troponin I. Troponin I is one of the most specific diagnostic serum biomarkers for myocardial infarction. The microfluidic impedance biosensor chip presented here consists of a microscope glass slide serving as base plate, sputtered electrodes, and a polydimethylsiloxane (PDMS) microchannel. Electrode functionalization protocols were developed considering a possible charge transfer through the sensing layer, in addition to analyte-specific binding by corresponding antibodies and reduction of nonspecific protein adsorption to prevent false-positive signals. Reagents tested for self-assembled monolayers (SAMs) on gold electrodes included thiolated hydrocarbons and thiolated oligonucleotides, where SAMs based on the latter showed a better performance. The corresponding antibody was covalently coupled on the SAM using carbodiimide chemistry. Sampling and measurement took only a few minutes. Application of a human serum albumin (HSA) sample, 1000 ng/mL, led to negligible impedance changes, while application of a troponin I sample, 1 ng/mL, led to a significant shift in the Nyquist plot. The results are promising regarding specific detection of clinically relevant concentrations of biomarkers, such as cardiac markers, with the newly developed microfluidic impedance biosensor chip.


Talanta ◽  
2014 ◽  
Vol 125 ◽  
pp. 29-35 ◽  
Author(s):  
Hua Zhang ◽  
Ying Sun ◽  
Shang Gao ◽  
Hanqi Zhang ◽  
Jia Zhang ◽  
...  

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