Nanomonitors: electrical immunoassays for protein biomarker profiling

被引:23
作者
Bothara, M. [1 ]
Venkatraman, V. [1 ]
Reddy, R. K. K. [1 ]
Barrett, T. [2 ]
Carruthers, J. [3 ]
Prasad, S. [1 ]
机构
[1] Portland State Univ, Dept Elect & Comp Engn, Portland, OR 97201 USA
[2] Oregon Hlth Sci Univ Portland, Dept Vet Affairs, Portland, OR 97209 USA
[3] Portland State Univ, Dept Phys, Portland, OR 97201 USA
关键词
biosensors; impedance spectroscopy; multiplexed detection; nanomembrane; protein;
D O I
10.2217/17435889.3.4.423
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Aims: The objective of this research is to develop a 'point-of-care' device for early disease diagnosis through protein biomarker characterization. Here, we present label-free, high sensitivity detection of proteins with the use of electrical immunciassays that we call nanomonitors. Materials & methods: The basis of the detection principle lies in the formation of an electrical double layer and its perturbations caused by proteins trapped in a nanoporous alumina membrane over a microelectrode array platform. Results & discussion: High sensitivity and rapid detection of study protein biomarkers for cardiovascular diseases, C-reactive protein (CRP) and myeloperoxidase (MPO) in pure and clinical samples through label-free electrical detection were achieved. CRP and MPO were detected in pure solutions with a lower detection limit of 200 pg/ml and 500 pg/ml, respectively. These two study proteins were also detected from multiplexed samples containing a mixture of both proteins as well as human serum samples. Conclusions: The performance parameters of the nanomonitors, such as speed of detection on the order of minutes, volume of reagents of a few microliters and low cost per assay are comparable to traditional assay methods, such as ELISA. In addition, nanomonitors also provide the advantages of being a label-free technique with large linear dynamic range of detection and a significant reduction in the size of assay, thus making it an ideal candidate for a clinical diagnostic 'lab-on-a-chip' device for protein biomarker profiling and hence early disease diagnosis.
引用
收藏
页码:423 / 436
页数:14
相关论文
共 28 条
[1]  
ABELOFF MA, 2000, CLIN ONCOLOGY, P76
[2]   Protein microchips: Use for immunoassay and enzymatic reactions [J].
Arenkov, P ;
Kukhtin, A ;
Gemmell, A ;
Voloshchuk, S ;
Chupeeva, V ;
Mirzabekov, A .
ANALYTICAL BIOCHEMISTRY, 2000, 278 (02) :123-131
[3]  
Bard A.J., 2001, ELECTROCHEMICAL METH, V2, P210
[4]  
BASZKIN A, 2001, PHYS CHEM BIOL INTER, P234
[5]  
Berggren C, 2001, ELECTROANAL, V13, P173, DOI 10.1002/1521-4109(200103)13:3<173::AID-ELAN173>3.0.CO
[6]  
2-B
[7]   Real-Time, label-free monitorine, of tumor antigen and serum antibody interactions [J].
Campagnolo, C ;
Meyers, KJ ;
Ryan, T ;
Atkinson, RC ;
Chen, YT ;
Scanlan, MJ ;
Ritter, G ;
Old, LJ ;
Batt, CA .
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS, 2004, 61 (03) :283-298
[8]   Biochemical effects of molecular crowding [J].
Chebotareva, NA ;
Kurganov, BI ;
Livanova, NB .
BIOCHEMISTRY-MOSCOW, 2004, 69 (11) :1239-+
[9]   Molecular crowding enhances native state stability and refolding rates of globular proteins [J].
Cheung, MS ;
Klimov, D ;
Thirumalai, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (13) :4753-4758
[10]   Development of an immunosensor for human ferritin, a nonspecific tumor marker, based on surface plasmon resonance [J].
Chou, SF ;
Hsu, WL ;
Hwang, JM ;
Chen, CY .
BIOSENSORS & BIOELECTRONICS, 2004, 19 (09) :999-1005