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使用具有相关光学读出功能的微纳霍尔磁力计检测目标单链DNA。

Detection of target ssDNA using a microfabricated Hall magnetometer with correlated optical readout.

作者信息

Hira Steven M, Aledealat Khaled, Chen Kan-Sheng, Field Mark, Sullivan Gerard J, Chase P Bryant, Xiong Peng, von Molnár Stephan, Strouse Geoffrey F

机构信息

Department of Chemistry and Biochemistry, The Florida State University, Tallahassee, FL 32306-4390, USA.

出版信息

J Biomed Biotechnol. 2012;2012:492730. doi: 10.1155/2012/492730. Epub 2012 Feb 13.

Abstract

Sensing biological agents at the genomic level, while enhancing the response time for biodetection over commonly used, optics-based techniques such as nucleic acid microarrays or enzyme-linked immunosorbent assays (ELISAs), is an important criterion for new biosensors. Here, we describe the successful detection of a 35-base, single-strand nucleic acid target by Hall-based magnetic transduction as a mimic for pathogenic DNA target detection. The detection platform has low background, large signal amplification following target binding and can discriminate a single, 350 nm superparamagnetic bead labeled with DNA. Detection of the target sequence was demonstrated at 364 pM (<2 target DNA strands per bead) target DNA in the presence of 36 μM nontarget (noncomplementary) DNA (<10 ppm target DNA) using optical microscopy detection on a GaAs Hall mimic. The use of Hall magnetometers as magnetic transduction biosensors holds promise for multiplexing applications that can greatly improve point-of-care (POC) diagnostics and subsequent medical care.

摘要

在基因组水平上检测生物制剂,同时比常用的基于光学的技术(如核酸微阵列或酶联免疫吸附测定(ELISA))提高生物检测的响应时间,是新型生物传感器的一个重要标准。在此,我们描述了通过基于霍尔效应的磁转导成功检测35个碱基的单链核酸靶标,以此模拟致病DNA靶标的检测。该检测平台背景低,靶标结合后信号大幅放大,并且能够区分单个标记有DNA的350 nm超顺磁性珠。在存在36 μM非靶标(非互补)DNA(<10 ppm靶标DNA)的情况下,使用砷化镓霍尔效应模拟物通过光学显微镜检测,在364 pM(每个珠子<2条靶标DNA链)的靶标DNA中证明了对靶标序列的检测。将霍尔磁力计用作磁转导生物传感器有望用于多重应用,这可以极大地改善即时护理(POC)诊断及后续医疗护理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ec3/3303874/ea3f4229d7f2/JBB2012-492730.001.jpg

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