An electrochemical aptamer-based biosensor targeting Plasmodium falciparum histidine-rich protein II for malaria diagnosis
Malaria is an infectious disease caused by parasitic protozoans from the genus Plasmodium, with the species P. falciparum causing the highest number of deaths worldwide. Rapid diagnostic tests (RDTs) have become critical in the management of malaria, but current RDTs that detect P. falciparum are pr...
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Published in | Biosensors & bioelectronics Vol. 192; p. 113472 |
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Main Authors | , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
15.11.2021
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Online Access | Get full text |
ISSN | 0956-5663 1873-4235 1873-4235 |
DOI | 10.1016/j.bios.2021.113472 |
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Abstract | Malaria is an infectious disease caused by parasitic protozoans from the genus Plasmodium, with the species P. falciparum causing the highest number of deaths worldwide. Rapid diagnostic tests (RDTs) have become critical in the management of malaria, but current RDTs that detect P. falciparum are primarily antibody-based, which can have drawbacks in cost and robustness. Here, we report the development of an electrochemical aptamer-based (E-AB) biosensing alternative. Through selective evolution of ligands by exponential enrichment, we identify DNA aptamers that bind specifically to P. falciparum histidine-rich protein II (PfHRP2). The aptamer is modified with a methylene blue reporter and attached to a gold sensor surface for square-wave voltammetry interrogation. Through this method we are able to quantify PfHRP2 in human serum with an LOD of 3.73 nM. We further demonstrate the biosensor is stable in serum buffers and reusable for multiple detection rounds. These findings provide a promising alternative to conventional PfHRP2 detection for malaria diagnosis, while also expanding the capabilities of E-AB biosensors.
•New DNA aptamers were selected against the malaria biomarker Plasmodium falciparum histidine rich protein 2 (PfHRP2).•Aptamer binding kinetics was rigorously characterized by surface plasmon resonance.•An electrochemical aptamer-based biosensor for reusable detection of the protein target was demonstrated.•PfHRP2 was detected with a detection limit of 3.73 nM. |
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AbstractList | Malaria is an infectious disease caused by parasitic protozoans from the genus Plasmodium, with the species P. falciparum causing the highest number of deaths worldwide. Rapid diagnostic tests (RDTs) have become critical in the management of malaria, but current RDTs that detect P. falciparum are primarily antibody-based, which can have drawbacks in cost and robustness. Here, we report the development of an electrochemical aptamer-based (E-AB) biosensing alternative. Through selective evolution of ligands by exponential enrichment, we identify DNA aptamers that bind specifically to P. falciparum histidine-rich protein II (PfHRP2). The aptamer is modified with a methylene blue reporter and attached to a gold sensor surface for square-wave voltammetry interrogation. Through this method we are able to quantify PfHRP2 in human serum with an LOD of 3.73 nM. We further demonstrate the biosensor is stable in serum buffers and reusable for multiple detection rounds. These findings provide a promising alternative to conventional PfHRP2 detection for malaria diagnosis, while also expanding the capabilities of E-AB biosensors.
•New DNA aptamers were selected against the malaria biomarker Plasmodium falciparum histidine rich protein 2 (PfHRP2).•Aptamer binding kinetics was rigorously characterized by surface plasmon resonance.•An electrochemical aptamer-based biosensor for reusable detection of the protein target was demonstrated.•PfHRP2 was detected with a detection limit of 3.73 nM. Malaria is an infectious disease caused by parasitic protozoans from the genus Plasmodium, with the species P. falciparum causing the highest number of deaths worldwide. Rapid diagnostic tests (RDTs) have become critical in the management of malaria, but current RDTs that detect P. falciparum are primarily antibody-based, which can have drawbacks in cost and robustness. Here, we report the development of an electrochemical aptamer-based (E-AB) biosensing alternative. Through selective evolution of ligands by exponential enrichment, we identify DNA aptamers that bind specifically to P. falciparum histidine-rich protein II (PfHRP2). The aptamer is modified with a methylene blue reporter and attached to a gold sensor surface for square-wave voltammetry interrogation. Through this method we are able to quantify PfHRP2 in human serum with an LOD of 3.73 nM. We further demonstrate the biosensor is stable in serum buffers and reusable for multiple detection rounds. These findings provide a promising alternative to conventional PfHRP2 detection for malaria diagnosis, while also expanding the capabilities of E-AB biosensors.Malaria is an infectious disease caused by parasitic protozoans from the genus Plasmodium, with the species P. falciparum causing the highest number of deaths worldwide. Rapid diagnostic tests (RDTs) have become critical in the management of malaria, but current RDTs that detect P. falciparum are primarily antibody-based, which can have drawbacks in cost and robustness. Here, we report the development of an electrochemical aptamer-based (E-AB) biosensing alternative. Through selective evolution of ligands by exponential enrichment, we identify DNA aptamers that bind specifically to P. falciparum histidine-rich protein II (PfHRP2). The aptamer is modified with a methylene blue reporter and attached to a gold sensor surface for square-wave voltammetry interrogation. Through this method we are able to quantify PfHRP2 in human serum with an LOD of 3.73 nM. We further demonstrate the biosensor is stable in serum buffers and reusable for multiple detection rounds. These findings provide a promising alternative to conventional PfHRP2 detection for malaria diagnosis, while also expanding the capabilities of E-AB biosensors. Malaria is an infectious disease caused by parasitic protozoans from the genus Plasmodium, with the species P. falciparum causing the highest number of deaths worldwide. Rapid diagnostic tests (RDTs) have become critical in the management of malaria, but current RDTs that detect P. falciparum are primarily antibody-based, which can have drawbacks in cost and robustness. Here, we report the development of an electrochemical aptamer-based (E-AB) biosensing alternative. Through selective evolution of ligands by exponential enrichment, we identify DNA aptamers that bind specifically to P. falciparum histidine-rich protein II (PfHRP2). The aptamer is modified with a methylene blue reporter and attached to a gold sensor surface for square-wave voltammetry interrogation. Through this method we are able to quantify PfHRP2 in human serum with an LOD of 3.73 nM. We further demonstrate the biosensor is stable in serum buffers and reusable for multiple detection rounds. These findings provide a promising alternative to conventional PfHRP2 detection for malaria diagnosis, while also expanding the capabilities of E-AB biosensors. |
ArticleNumber | 113472 |
Author | Lee, Megan Cheung, Yee-Wai Tanner, Julian Alexander Figueroa-Miranda, Gabriela Lo, Young Wang, Lin Liang, Shaolin Mayer, Dirk |
Author_xml | – sequence: 1 givenname: Young surname: Lo fullname: Lo, Young organization: School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 2 givenname: Yee-Wai surname: Cheung fullname: Cheung, Yee-Wai organization: School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 3 givenname: Lin surname: Wang fullname: Wang, Lin organization: School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 4 givenname: Megan surname: Lee fullname: Lee, Megan organization: School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China – sequence: 5 givenname: Gabriela surname: Figueroa-Miranda fullname: Figueroa-Miranda, Gabriela organization: Institute of Biological Information Processing, Bioelectronics (IBI-3), Forschungszentrum Jülich GmbH, Jülich, Germany – sequence: 6 givenname: Shaolin surname: Liang fullname: Liang, Shaolin organization: "Mobile Health” Ministry of Education-China Mobile Joint Laboratory, Xiangya Hospital, Central South University, Changsha, China – sequence: 7 givenname: Dirk surname: Mayer fullname: Mayer, Dirk organization: Institute of Biological Information Processing, Bioelectronics (IBI-3), Forschungszentrum Jülich GmbH, Jülich, Germany – sequence: 8 givenname: Julian Alexander orcidid: 0000-0002-5459-1526 surname: Tanner fullname: Tanner, Julian Alexander email: jatanner@hku.hk organization: School of Biomedical Sciences, LKS Faculty of Medicine, The University of Hong Kong, Hong Kong, China |
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Keywords | Electrochemical aptamer-based biosensor Rapid diagnostic test Malaria Plasmodium falciparum histidine-Rich protein II Aptasensor Square-wave voltammetry |
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SubjectTerms | Aptasensor biosensors blood serum Electrochemical aptamer-based biosensor electrochemistry gold humans infectious diseases ligands Malaria methylene blue nucleotide aptamers Plasmodium falciparum Plasmodium falciparum histidine-Rich protein II Rapid diagnostic test Square-wave voltammetry voltammetry |
Title | An electrochemical aptamer-based biosensor targeting Plasmodium falciparum histidine-rich protein II for malaria diagnosis |
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