Novel biosensor chip for simultaneous detection of DNA-carcinogen adducts with low-temperature fluorescence

被引:40
作者
Grubor, NM
Shinar, R
Jankowiak, R [1 ]
Porter, MD
Small, GJ
机构
[1] Iowa State Univ Sci & Technol, Ames Lab, US DOE, Ames, IA 50011 USA
[2] Iowa State Univ Sci & Technol, Dept Chem, Ames, IA 50011 USA
[3] Iowa State Univ Sci & Technol, Microelect Res Ctr, Ames, IA 50011 USA
[4] Iowa State Univ Sci & Technol, Microanalyt Instrumentat Ctr, Ames, IA 50011 USA
关键词
biosensor; fluorescence detection; fluorescence line-narrowing spectroscopy; DNA adducts;
D O I
10.1016/S0956-5663(03)00274-4
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A monoclonal antibody (MAb)-gold biosensor chip with low-temperature laser-induced fluorescence detection for analysis of DNA-carcinogen adducts is described. Optimization of the detection limit, dynamic range, and biosensing applicability of the MAb-gold biosensor chip was achieved by: (1) using dithiobis(succinimidyl propionate (DSP)) as a protein linker and (2) employing recombinant protein A to provide oriented immobilization of the MAbs. The use of DSP, which has a short methylene chain length, led to faster protein binding kinetics and higher protein surface density than a longer dithiobis(succinimidyl undecanoate) (DSU) linker. The incorporation of recombinant protein A increased the distance between the oriented MAb-bound analytes and the gold surface. The increased distance minimized fluorescence quenching, resulting in about a 10-fold increase in the fluorescence signal in comparison with a chip without protein A. The improved chip architecture was used to demonstrate that biosensing of two structurally similar benzo[a]pyrene (BP)-derived DNA adducts, BP-6-N7Gua and BP-diolepoxide-10-N(2)dG, bound to two specific MAbs immobilized from a mixture at the same address on the chip, is feasible. These mutagenic adducts are formed by one-electron oxidation and monooxygenation pathways, and are depurinating and stable DNA adducts, respectively. It is shown that the DNA adducts can be easily identified at the same address using time-resolved, low-temperature laser-based fluorescence spectroscopy. The current limit of detection is in the low femtomole range. These results indicate that a single biosensor chip consisting of a Au/DSP/protein A/MAb nanoassembly, with analyte-specific MAbs and low-temperature fluorescence detection should be suitable for simultaneous detection and quantitation of the above adducts, as well as the luminescent antigens for which selective MAbs exist. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:547 / 556
页数:10
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