A Modular, DNA-Based Beacon for Single-Step Fluorescence Detection of Antibodies and Other Proteins

被引:93
|
作者
Ranallo, Simona [1 ]
Rossetti, Marianna [1 ]
Plaxco, Kevin W. [2 ,3 ]
Vallee-Belisle, Alexis [4 ]
Ricci, Francesco [1 ]
机构
[1] Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
[2] Univ Calif Santa Barbara, Ctr Bioengn, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Chem & Biochem, Santa Barbara, CA 93106 USA
[4] Univ Montreal, Dept Chim, Lab Biosensors & Nanomachines, Montreal, PQ H3C 3J7, Canada
基金
加拿大自然科学与工程研究理事会; 美国国家卫生研究院; 欧洲研究理事会; 瑞典研究理事会;
关键词
antibodies; aptamers; DNA nanotechnology; fluorescence; molecular devices; EXCLUSIVE DOMAIN INTERACTIONS; QUANTITATIVE DETECTION; MOLECULAR BEACONS; WHOLE-BLOOD; HOMOGENEOUS IMMUNOASSAYS; FRAGMENT COMPLEMENTATION; GLOBAL HEALTH; BINDING; BIOSENSORS; SWITCHES;
D O I
10.1002/anie.201505179
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A versatile platform for the one-step fluorescence detection of both monovalent and multivalent proteins has been developed. This system is based on a conformation-switching stem-loop DNA scaffold that presents a small-molecule, polypeptide, or nucleic-acid recognition element on each of its two stem strands. The steric strain associated with the binding of one (multivalent) or two (monovalent) target molecules to these elements opens the stem, enhancing the emission of an attached fluorophore/quencher pair. The sensors respond rapidly (<10min) and selectively, enabling the facile detection of specific proteins even in complex samples, such as blood serum. The versatility of the platform was demonstrated by detecting five bivalent proteins (four antibodies and the chemokine platelet-derived growth factor) and two monovalent proteins (a Fab fragment and the transcription factor TBP) with low nanomolar detection limits and no detectable cross-reactivity.
引用
收藏
页码:13214 / 13218
页数:5
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