Acoustic wave biosensor for the detection of the breast and prostate cancer metastasis biomarker protein PTHrP

被引:31
作者
Crivianu-Gaita, Victor [1 ]
Aamer, Mohamed [1 ]
Posaratnanathan, Roy T. [1 ]
Romaschin, Alexander [2 ]
Thompson, Michael [1 ]
机构
[1] Univ Toronto, Dept Chem, Toronto, ON M5S 3H6, Canada
[2] St Michaels Hosp, Clin Biochem, 30 Bond St, Toronto, ON M5B 1W8, Canada
关键词
Acoustic wave sensor; Parathyroid hormone-related peptide; Fab' fragments; Antibodies; Biosensor; Cancer metastasis; SITE-DIRECTED IMMOBILIZATION; LABEL-FREE DETECTION; ANTIBODY FRAGMENTS; FAB'-FRAGMENTS; PEPTIDE; MOLECULES; DEVICES; ANTIGEN; GROWTH; SERUM;
D O I
10.1016/j.bios.2015.11.031
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
There are currently no biosensors that are able to reliably detect the process of cancer metastasis. We describe the first label-free real-time ultra-high frequency acoustic wave biosensor prototype capable of detecting the breast and prostate cancer metastasis biomarker, parathyroid hormone-related peptide (PTHrP). Two different linkers - 11-trichlorosilyl-undecanoic acid pentafluorophenyl ester (PFP) and S-(11-trichlorosilyl-undecanyl)-benzothiosulfonate (TUBTS) - were used to immobilize whole anti-PTHrP antibodies and Fab' fragments to surfaces as biorecognition elements. The biosensor surfaces were optimized using X-ray photoelectron spectroscopy (XPS) and the ultra-high frequency electromagnetic piezoelectric acoustic sensor (EMPAS). One optimized whole antibody-based surface (PFP/protein G'/whole antibodies/ethanolamine) and one optimized Fab' fragment-based surface (TUBTS/Fab' fragments) were tested as biosensors. It was determined that an in-line injection of bovine serum albumin prior to analyte injection yielded the most minimally fouling surfaces. Each surface was tested with no mass amplification and with sandwich-type secondary antibody mass amplification. The whole antibody based mass-amplified biosensor yielded the lowest limit of detection (61 ng/mL), highest sensitivity, and a linear range from 61 ng/mL to 100 pg/mL. However, the Fab' fragment-based biosensor displayed better regenerability as a loss of 20% of the initial analyte signal intensity was observed with each subsequent injection. The whole antibody-based biosensor was only capable of producing an analyte signal in the first injection. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:92 / 99
页数:8
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