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Amplified QCM-D biosensor for protein based on aptamer-functionalized gold nanoparticles.
Biosens Bioelectron. 2010 Oct 15; 26(2):575-9.BB

Abstract

A highly sensitive quartz crystal microbalance with dissipation monitoring (QCM-D) biosensor for protein was developed using aptamer-functionalized gold nanoparticles (Apt-GNPs) for amplification. Human α-thrombin, an important physiological protease found in blood, was chosen as the target protein. Captured by immobilized aptamers, thrombin was determined on-line using Apt-GNPs to enhance both frequency and dissipation signals. The fabricated sandwich of aptamer/thrombin/Apt-GNPs on chip surface was confirmed by atomic force microscopy (AFM). Compared to direct assay, the detection limit for thrombin was down to 0.1 nM, yielding about 2 orders of magnitude improvement in sensitivity. This aptamer-based QCM-D biosensor also showed good selectivity and repeatability in complex matrix. For the first time, the dual-signal enhancement of Apt-GNPs on QCM-D sensing was demonstrated, and such design could provide a promising detection strategy for proteins with two binding sites.

Authors+Show Affiliations

Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of the Ministry of Education, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

20692147

Citation

Chen, Qiang, et al. "Amplified QCM-D Biosensor for Protein Based On Aptamer-functionalized Gold Nanoparticles." Biosensors & Bioelectronics, vol. 26, no. 2, 2010, pp. 575-9.
Chen Q, Tang W, Wang D, et al. Amplified QCM-D biosensor for protein based on aptamer-functionalized gold nanoparticles. Biosens Bioelectron. 2010;26(2):575-9.
Chen, Q., Tang, W., Wang, D., Wu, X., Li, N., & Liu, F. (2010). Amplified QCM-D biosensor for protein based on aptamer-functionalized gold nanoparticles. Biosensors & Bioelectronics, 26(2), 575-9. https://doi.org/10.1016/j.bios.2010.07.034
Chen Q, et al. Amplified QCM-D Biosensor for Protein Based On Aptamer-functionalized Gold Nanoparticles. Biosens Bioelectron. 2010 Oct 15;26(2):575-9. PubMed PMID: 20692147.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Amplified QCM-D biosensor for protein based on aptamer-functionalized gold nanoparticles. AU - Chen,Qiang, AU - Tang,Wei, AU - Wang,Dingzhong, AU - Wu,Xiaojie, AU - Li,Na, AU - Liu,Feng, Y1 - 2010/07/17/ PY - 2010/05/14/received PY - 2010/07/05/revised PY - 2010/07/11/accepted PY - 2010/8/10/entrez PY - 2010/8/10/pubmed PY - 2011/2/8/medline SP - 575 EP - 9 JF - Biosensors & bioelectronics JO - Biosens Bioelectron VL - 26 IS - 2 N2 - A highly sensitive quartz crystal microbalance with dissipation monitoring (QCM-D) biosensor for protein was developed using aptamer-functionalized gold nanoparticles (Apt-GNPs) for amplification. Human α-thrombin, an important physiological protease found in blood, was chosen as the target protein. Captured by immobilized aptamers, thrombin was determined on-line using Apt-GNPs to enhance both frequency and dissipation signals. The fabricated sandwich of aptamer/thrombin/Apt-GNPs on chip surface was confirmed by atomic force microscopy (AFM). Compared to direct assay, the detection limit for thrombin was down to 0.1 nM, yielding about 2 orders of magnitude improvement in sensitivity. This aptamer-based QCM-D biosensor also showed good selectivity and repeatability in complex matrix. For the first time, the dual-signal enhancement of Apt-GNPs on QCM-D sensing was demonstrated, and such design could provide a promising detection strategy for proteins with two binding sites. SN - 1873-4235 UR - https://www.unboundmedicine.com/medline/citation/20692147/Amplified_QCM_D_biosensor_for_protein_based_on_aptamer_functionalized_gold_nanoparticles_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0956-5663(10)00409-4 DB - PRIME DP - Unbound Medicine ER -