Antibody biosensors for the measurement and characterization of soluble CD147 molecules
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 simultane...
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th-cmuir.6653943832-627422018-11-29T07:50:39Z Antibody biosensors for the measurement and characterization of soluble CD147 molecules Witida Laopajon Nuchjira Takheaw Saichit Khummuang Tanyaluck Kampoun Kantinan Cheunsirikulchai Watchara Kasinrerk Supansa Pata Immunology and Microbiology Medicine 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 CD147 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 sCD147 isoforms. For the single Ab-biosensor system, monoclonal antibodies specific for CD147 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 CD147 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. 2018-11-29T07:44:53Z 2018-11-29T07:44:53Z 2018-09-01 Journal 0125877X 2-s2.0-85054440481 10.12932/AP-150217-0022 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054440481&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62742 |
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Immunology and Microbiology Medicine Witida Laopajon Nuchjira Takheaw Saichit Khummuang Tanyaluck Kampoun Kantinan Cheunsirikulchai Watchara Kasinrerk Supansa Pata Antibody biosensors for the measurement and characterization of soluble CD147 molecules |
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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 CD147 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 sCD147 isoforms. For the single Ab-biosensor system, monoclonal antibodies specific for CD147 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 CD147 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. |
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Witida Laopajon Nuchjira Takheaw Saichit Khummuang Tanyaluck Kampoun Kantinan Cheunsirikulchai Watchara Kasinrerk Supansa Pata |
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Witida Laopajon Nuchjira Takheaw Saichit Khummuang Tanyaluck Kampoun Kantinan Cheunsirikulchai Watchara Kasinrerk Supansa Pata |
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Witida Laopajon |
title |
Antibody biosensors for the measurement and characterization of soluble CD147 molecules |
title_short |
Antibody biosensors for the measurement and characterization of soluble CD147 molecules |
title_full |
Antibody biosensors for the measurement and characterization of soluble CD147 molecules |
title_fullStr |
Antibody biosensors for the measurement and characterization of soluble CD147 molecules |
title_full_unstemmed |
Antibody biosensors for the measurement and characterization of soluble CD147 molecules |
title_sort |
antibody biosensors for the measurement and characterization of soluble cd147 molecules |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054440481&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/62742 |
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