Femtomolar detection of nucleic acid based on functionalized gold nanoparticles

Author:

Huang Jiaoqi1,Zhang Yang2,Lin Zhongquan1,Liu Wei1,Chen Xueping1,Liu Yu1,Tian Huiyan1,Liu Qiqian3,Gillibert Raymond3,Spadavecchia Jolanda3,Djaker Nadia3,de la Chapelle Marc Lamy14,Xiang Yang56,Fu Weiling6

Affiliation:

1. Department of Laboratory Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), Chongqing 400038, China

2. Department of Laboratory Medicine, Chongqing General Hospital, Chongqing 400038, China

3. Université Paris 13, Sorbonne Paris Cité, UFR SMBH, Laboratoire CSPBAT, CNRS (UMR 7244), 74 rue Marcel Cachin, F-93017 Bobigny, France

4. Institut des Molécules et Matériaux du Mans (IMMM – UMR CNRS 6283), Université du Mans, Avenue Olivier Messiaen, 72085 Le Mans, France

5. Department of Clinical Microbiology and Immunology, Faculty of Pharmacy and Medical Laboratory Sciences, Third Military Medical University (Army Medical University), Chongqing 400038, China

6. Department of Laboratory Medicine, Southwest Hospital, Third Military Medical University (Army Medical University), No. 29 Gaotanyan street, Shapingba, Chongqing 400038, China

Abstract

AbstractDeoxyribonucleic acid (DNA) detection is essential for the accurate and early diagnosis of a disease. In this study, a femtomolar DNA detection method based on the exploitation of the localized surface plasmon (LSP) resonance of gold nanoparticles (AuNPs) was developed. We prepared Poly Ethylen Glycol (PEG) functionalized AuNPs with a specific DNA capture probe (CP) directly modified on the gold surface. Two strategies are proposed using different kinds of CP to detect the target DNA (tDNA). In the first strategy, CP is the complementary of the complete sequence of the DNA (CCP method). For the second strategy, we used two CPs, which were half complementary to tDNA, and these were hybridized with tDNA to form sandwich structures (MIX method). The results showed that our detection methods are highly sensitive and that the limits of detection of 124 am and 2.54 fm tDNA can be reached when using the CCP and MIX methods, respectively. In addition, the specificity of our two strategies is also demonstrated with mismatched DNAs. The proposed method provides a simple, fast, sensitive and specific DNA biosensor, which has the potential to be used for point-of-care tests (POCT).

Publisher

Walter de Gruyter GmbH

Subject

Electrical and Electronic Engineering,Atomic and Molecular Physics, and Optics,Electronic, Optical and Magnetic Materials,Biotechnology

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