Label-free optical bifunctional oligonucleotide probe for homogeneous amplification detection of disease markers
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| Title: | Label-free optical bifunctional oligonucleotide probe for homogeneous amplification detection of disease markers |
|---|---|
| Authors: | Feng, Kejun1,2, Qiu, Li-Ping1, Yang, Yifeng1, Wu, Zai-Sheng1 wuzaisheng@163.com, Shen, Guo-Li1 glshen@hnu.cn, Yu, Ru-Qin1 |
| Source: | Biosensors & Bioelectronics. Nov2011, Vol. 29 Issue 1, p66-75. 10p. |
| Subjects: | Nucleic acid probes, Biomarkers, Biosensors, Gene amplification, p53 antioncogene, Polymerization |
| Abstract: | Abstract: Oligonucleotide-based detection schemes that avoid chemical modification possess significant advantages, including simplified design, intrinsic affinity for targets, low cost and ease to extend applications. In this contribution, we developed a label-free self-locked bifunctional oligonucleotide probe (signaling probe) for the detection of different disease markers in parallel. Two signal enhancement techniques based on isothermal circular strand-displacement polymerization reaction, cyclical nucleic acid strand-displacement polymerization (CNDP) and cyclical common (nonnucleic acid) target-displacement polymerization (CCDP), were employed to implement the amplification assay for p53 gene and PDGF-BB, respectively. The attractive assay properties confirmed the effectiveness of isothermal polymerization in common biosensing systems without evolving any chemical modification: PDGF could be detected down to 0.87ng/mL, and a dynamic response range of 8–5000ng/mL was achieved; The capability to screen the p53 gene was also considerably improved, including the detection limit, sensitivity, dynamic range and so on. Moreover, because no any chemical modification of the signaling probe was acquired and different targets were separately detected in homogeneous solution. This interrogating platform exhibits the design flexibility, convenience, simplicity and cost-effectiveness. The success achieved here is expected to serve as a significant step toward the development of robust label-free oligonucleotide probes in biomarker profiling and disease diagnostics. [Copyright &y& Elsevier] |
| Copyright of Biosensors & Bioelectronics is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.) | |
| Database: | Engineering Source |
| FullText | Text: Availability: 0 |
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| Header | DbId: egs DbLabel: Engineering Source An: 65940079 AccessLevel: 6 PubType: Academic Journal PubTypeId: academicJournal PreciseRelevancyScore: 0 |
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| Items | – Name: Title Label: Title Group: Ti Data: Label-free optical bifunctional oligonucleotide probe for homogeneous amplification detection of disease markers – Name: Author Label: Authors Group: Au Data: <searchLink fieldCode="AR" term="%22Feng%2C+Kejun%22">Feng, Kejun</searchLink><relatesTo>1,2</relatesTo><br /><searchLink fieldCode="AR" term="%22Qiu%2C+Li-Ping%22">Qiu, Li-Ping</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Yang%2C+Yifeng%22">Yang, Yifeng</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Wu%2C+Zai-Sheng%22">Wu, Zai-Sheng</searchLink><relatesTo>1</relatesTo><i> wuzaisheng@163.com</i><br /><searchLink fieldCode="AR" term="%22Shen%2C+Guo-Li%22">Shen, Guo-Li</searchLink><relatesTo>1</relatesTo><i> glshen@hnu.cn</i><br /><searchLink fieldCode="AR" term="%22Yu%2C+Ru-Qin%22">Yu, Ru-Qin</searchLink><relatesTo>1</relatesTo> – Name: TitleSource Label: Source Group: Src Data: <searchLink fieldCode="JN" term="%22Biosensors+%26+Bioelectronics%22">Biosensors & Bioelectronics</searchLink>. Nov2011, Vol. 29 Issue 1, p66-75. 10p. – Name: Subject Label: Subjects Group: Su Data: <searchLink fieldCode="DE" term="%22Nucleic+acid+probes%22">Nucleic acid probes</searchLink><br /><searchLink fieldCode="DE" term="%22Biomarkers%22">Biomarkers</searchLink><br /><searchLink fieldCode="DE" term="%22Biosensors%22">Biosensors</searchLink><br /><searchLink fieldCode="DE" term="%22Gene+amplification%22">Gene amplification</searchLink><br /><searchLink fieldCode="DE" term="%22p53+antioncogene%22">p53 antioncogene</searchLink><br /><searchLink fieldCode="DE" term="%22Polymerization%22">Polymerization</searchLink> – Name: Abstract Label: Abstract Group: Ab Data: Abstract: Oligonucleotide-based detection schemes that avoid chemical modification possess significant advantages, including simplified design, intrinsic affinity for targets, low cost and ease to extend applications. In this contribution, we developed a label-free self-locked bifunctional oligonucleotide probe (signaling probe) for the detection of different disease markers in parallel. Two signal enhancement techniques based on isothermal circular strand-displacement polymerization reaction, cyclical nucleic acid strand-displacement polymerization (CNDP) and cyclical common (nonnucleic acid) target-displacement polymerization (CCDP), were employed to implement the amplification assay for p53 gene and PDGF-BB, respectively. The attractive assay properties confirmed the effectiveness of isothermal polymerization in common biosensing systems without evolving any chemical modification: PDGF could be detected down to 0.87ng/mL, and a dynamic response range of 8–5000ng/mL was achieved; The capability to screen the p53 gene was also considerably improved, including the detection limit, sensitivity, dynamic range and so on. Moreover, because no any chemical modification of the signaling probe was acquired and different targets were separately detected in homogeneous solution. This interrogating platform exhibits the design flexibility, convenience, simplicity and cost-effectiveness. The success achieved here is expected to serve as a significant step toward the development of robust label-free oligonucleotide probes in biomarker profiling and disease diagnostics. [Copyright &y& Elsevier] – Name: AbstractSuppliedCopyright Label: Group: Ab Data: <i>Copyright of Biosensors & Bioelectronics is the property of Elsevier B.V. and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.) |
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| RecordInfo | BibRecord: BibEntity: Identifiers: – Type: doi Value: 10.1016/j.bios.2011.07.068 Languages: – Code: eng Text: English PhysicalDescription: Pagination: PageCount: 10 StartPage: 66 Subjects: – SubjectFull: Nucleic acid probes Type: general – SubjectFull: Biomarkers Type: general – SubjectFull: Biosensors Type: general – SubjectFull: Gene amplification Type: general – SubjectFull: p53 antioncogene Type: general – SubjectFull: Polymerization Type: general Titles: – TitleFull: Label-free optical bifunctional oligonucleotide probe for homogeneous amplification detection of disease markers Type: main BibRelationships: HasContributorRelationships: – PersonEntity: Name: NameFull: Feng, Kejun – PersonEntity: Name: NameFull: Qiu, Li-Ping – PersonEntity: Name: NameFull: Yang, Yifeng – PersonEntity: Name: NameFull: Wu, Zai-Sheng – PersonEntity: Name: NameFull: Shen, Guo-Li – PersonEntity: Name: NameFull: Yu, Ru-Qin IsPartOfRelationships: – BibEntity: Dates: – D: 15 M: 11 Text: Nov2011 Type: published Y: 2011 Identifiers: – Type: issn-print Value: 09565663 Numbering: – Type: volume Value: 29 – Type: issue Value: 1 Titles: – TitleFull: Biosensors & Bioelectronics Type: main |
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