Biomolecular detection, tracking, and manipulation using a magnetic nanoparticle-quantum dot platform

被引:8
|
作者
Mahajan, Kalpesh D. [1 ]
Ruan, Gang [1 ,2 ]
Vieira, Greg [3 ,4 ]
Porter, Thomas [1 ]
Chalmers, Jeffrey J. [1 ]
Sooryakumar, R. [3 ]
Winter, Jessica O. [1 ,5 ]
机构
[1] Ohio State Univ, William G Lowrie Dept Chem & Biomol Engn, Columbus, OH 43210 USA
[2] Nanjing Univ, Dept Biomed Engn, Coll Engn & Appl Sci, Nanjing, Peoples R China
[3] Ohio State Univ, Dept Phys, 174 W 18th Ave, Columbus, OH 43210 USA
[4] Rhodes Coll, Dept Phys, Memphis, TN 38112 USA
[5] Ohio State Univ, Dept Biomed Engn, Columbus, OH 43210 USA
基金
美国国家科学基金会;
关键词
RESONANCE ENERGY-TRANSFER; FLUORESCENCE; NANOSENSORS; PROBE;
D O I
10.1039/c9tb02481f
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Fluorescent and magnetic materials play a significant role in biosensor technology, enabling sensitive quantification and separations with applications in diagnostics, purification, quality control, and therapeutics. Here, we present a magneto-fluorescent biosensor/separations platform consisting of quantum dots (QDs) and superparamagnetic iron oxide nanoparticles (SPIONs) that are separately encapsulated in amphiphihc block co-polymer micelles conjugated to DNA or protein (i.e., single-stranded (ss) DNA derived from the mRNA of the tumor suppressor protein p53 or avidin protein). Analytes were detected via an aggregation sandwich assay upon binding of atleast 1 QD and 1 SPION-containing micelle to result in a fluorescent/magnetic composite. Multiplexed isolation of protein and DNA biomolecules was demonstrated by using QDs of varying emission wavelength; QD fluorescence intensity could be correlated with analyte concentration. Sequential or parallel biomolecule separation was achieved by adding appropriately functionalized SPION-containing micelles and applying user-controlled magnetic fields via patterned magnetic disks and wires. QD fluorescence was used to continuously visualize analyte separation during this process. This QD/SPION platform is simple to use, demonstrates similar to 10(-16) M sensitivity in analyte detection (comparable to competing QD biosensors based on energy transfer) with specificity against 1 and 2 basepair mismatches in DNA detection, molecular separations capability in solutions of similar to 10(-10) M, and permits simultaneous or parallel, multiplexed separation of protein and DNA. Thus, this versatile platform enables self-assembly-based rapid, sensitive, and specific detection and separation of biomolecules, simultaneously and with real-time visualization. This technology demonstrates potential for nanoscale assembly, biosensing, and bioseparations.
引用
收藏
页码:3534 / 3541
页数:8
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