共 33 条
Label-free, multiplexed virus detection using spectral reflectance imaging
被引:47
作者:
Lopez, Carlos A.
[1
]
Daaboul, George G.
[2
]
Vedula, Rahul S.
[1
]
Oezkumur, Emre
[3
]
Bergstein, David A.
[4
]
Geisbert, Thomas W.
[5
,6
,8
]
Fawcett, Helen E.
[7
]
Goldberg, Bennett B.
[1
,2
,9
]
Connor, John H.
[7
,8
]
Uenlue, M. Selim
[1
,2
,9
]
机构:
[1] Boston Univ, Dept Elect & Comp Engn, Boston, MA 02215 USA
[2] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[3] Harvard Univ, Massachusetts Gen Hosp, Ctr Canc, Ctr Engn Med, Boston, MA 02114 USA
[4] Zoiray Technol Inc, Boston, MA USA
[5] Univ Texas Galveston, Med Branch, Galveston Natl Lab, Galveston, TX 77550 USA
[6] Univ Texas Galveston, Med Branch, Dept Microbiol & Immunol, Galveston, TX 77550 USA
[7] Boston Univ, Photon Ctr, Boston, MA 02215 USA
[8] Boston Univ, Sch Med, Dept Microbiol, Boston, MA 02118 USA
[9] Boston Univ, Dept Phys, Boston, MA 02215 USA
基金:
美国国家卫生研究院;
关键词:
Virus detection;
Label-free;
Interferometry;
Biosensor;
High-throughput;
Microarray;
Quantitative sensing;
VESICULAR STOMATITIS-VIRUS;
MICROARRAY APPLICATIONS;
ELECTRON-MICROSCOPY;
INFLUENZA-VIRUS;
MOUTH-DISEASE;
BIOSENSORS;
DIAGNOSIS;
DNA;
FUTURE;
AGENTS;
D O I:
10.1016/j.bios.2011.01.019
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
We demonstrate detection of whole viruses and viral proteins with a new label-free platform based on spectral reflectance imaging. The Interferometric Reflectance Imaging Sensor (IRIS) has been shown to be capable of sensitive protein and DNA detection in a real time and high-throughput format. Vesicular stomatitis virus (VSV) was used as the target for detection as it is well-characterized for protein composition and can be modified to express viral coat proteins from other dangerous, highly pathogenic agents for surrogate detection while remaining a biosafety level 2 agent. We demonstrate specific detection of intact VSV virions achieved with surface-immobilized antibodies acting as capture probes which is confirmed using fluorescence imaging. The limit of detection is confirmed down to 3.5 x 10(5) plaque-forming units/mL (PFUs/mL). To increase specificity in a clinical scenario, both the external glycoprotein and internal viral proteins were simultaneously detected with the same antibody arrays with detergent-disrupted purified VSV and infected cell lysate solutions. Our results show sensitive and specific virus detection with a simple surface chemistry and minimal sample preparation on a quantitative label-free interferometric platform. (C) 2011 Elsevier B.V. All rights reserved.
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页码:3432 / 3437
页数:6
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