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Antibody biosensors for the measurement and characterization of soluble CD 147 molecules
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by นพพร ม่วงระย้า  
Metadata
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
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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
PDF
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
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