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Biosensors and Bioelectronics
Article . 2014 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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Microarray based on autodisplayed Ro proteins for medical diagnosis of systemic lupus erythematosus (SLE)

Authors: Gu, Yoo; Ji-Hong, Bong; Sinyoung, Kim; Joachim, Jose; Jae-Chul, Pyun;

Microarray based on autodisplayed Ro proteins for medical diagnosis of systemic lupus erythematosus (SLE)

Abstract

A microarray-based immunoassay for the detection of autoantibodies against Ro protein was developed using Escherichia coli with autodisplayed Ro proteins (Ro(+)-E. coli). Patient serum usually contains various antibodies against the outer membrane components of E. coli as well as autoantibodies against the Ro protein. Therefore, the conventional immunoassay based on Ro(+)-E. coli requires both wild type E. coli (blank test) and Ro(+)-E. coli, and both strains of E. coli must be prepared in situ for each individual test serum. In this study, we tested the feasibility of using several types of animal sera as a replacement for individual human sera. An immunoassay without the blank test was developed using Ro(+)-E. coli by (1) blocking with rabbit serum, and (2) cleaving the Fc region from antibodies using papain. Modified E. coli with autodisplayed Ro protein was immobilized to a surface-modified microplate and the applicability of the immunoassay without the blank test was demonstrated using sera from patients with systemic lupus erythematosus (SLE). Using this approach, a microarray-based fluorescence immunoassay with immobilized Ro(+)-E. coli was able to detect anti-Ro autoantibodies in SLE patient sera with high specificity and selectivity and improved efficiency.

Related Organizations
Keywords

abbits, Cells, Escherichia coli/chemistry, Fluoroimmunoassay, Protein Array Analysis, Autodisplay, 610, Biosensing Techniques, Microarray, Ro-protein, Sensitivity and Specificity, Fluoroimmunoassay/methods, Fluorescence immunoassay, Protein Array Analysis/methods*, Escherichia coli, Animals, Humans, Lupus Erythematosus, Systemic, Autoantibodies, Immobilized/chemistry, Lupus Erythematosus, Cells, Immobilized, Ribonucleoproteins, Autoantibodies/analysis*, Systemic/diagnosis*, Ribonucleoproteins/immunology*, Systemic lupus erythematosus (SLE), Biosensing Techniques/methods*, Rabbits, Autoimmune

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    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
29
Top 10%
Top 10%
Top 10%
Green