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Antibody biosensors for the measurement and characterization of soluble CD 147 molecules
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Document Title
Antibody biosensors for the measurement and characterization of soluble CD 147 molecules
Author
Laopajon W, Takheaw N, Khununuang S, Kampoun T, Cheunsirikulchai K, Kasinrerk W, Pata S
Name from Authors Collection
Affiliations
Chiang Mai University; Chiang Mai University; National Science & Technology Development Agency - Thailand; National Center Genetic Engineering & Biotechnology (BIOTEC)
Type
Article
Source Title
ASIAN PACIFIC JOURNAL OF ALLERGY AND IMMUNOLOGY
ISSN
0125-877X
Year
2018
Volume
36
Issue
4
Open Access
Bronze
Publisher
ALLERGY IMMUNOL SOC THAILAND,
DOI
10.12932/AP-150217-0022
Format
Abstract
Background: Soluble CD147 (sCD147) is the shed form of membrane-bound CD147, which is involved in the regulation of cellular functions. The presence of sCD147 in body fluids is associated with several diseases. Objective: In this study, we aimed to establish antibody (Ab) biosensors for the simultaneous differential detection of the general and truncated forms of sCD147. Method: By combining biolayer interferometry technology (BLItz) and different anti-CD147 monoclonal antibodies (mAbs) specific to different extracellular domains of the CD 147 molecule, Ab-based biosensors were established to rapidly measure and characterize sCD147 isoforms. Results: Two types of Ab-biosensors, desginated the single Ab-biosensor and double Ab-biosensor, were established for the measurment and characterization of sCD 147 isoforms. For the single Ab-biosensor system, monoclonal antibodies specific for CD 147 domain 1 (D1) or domain 2 (D2) were immobilized on the sensor tips and used for the quantification of sCD147 using a BLItz optical interferometric biosensor. For the double Ab-biosensor system, following the single Ab-biosensor step, secondary anti-CD147 mAbs specific for each domain of the CD 147 molecule were added and monitored by a BLItz biosensor. By combining the results obtained from the single Ab-and double Ab-biosensors, sCD147 isoforms including the general form (D1 linked to D2) and the truncated forms (sCD147 containing D1 or D2) could be determined. Conclusions: This method may be a beneficial tool for the determination of sCD147 isoforms for disease diagnosis and prognosis as well as for the definition of the cellular mechanisms of the immune system.
Keyword
Biosensor | CD 147 | Isoform | Monoclonal antibody | soluble CD 147
Funding Sponsor
Faculty of Associated Medical Sciences, Chiang Mai University; Thailand Research Fund [TRG5780017, PHD/0121/2557]; TRF Senior Research Scholar [RTA5980007]; Chiang Mai University [PHD/0064/2555]
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WOS