Protein microarrays with carbon nanotubes as multicolor Raman labels

被引:259
作者
Chen, Zhuo [1 ,2 ]
Tabakman, Scott M. [1 ,2 ]
Goodwin, Andrew P. [1 ,2 ]
Kattah, Michael G. [3 ]
Daranciang, Dan [1 ,2 ]
Wang, Xinran [1 ,2 ]
Zhang, Guangyu [1 ,2 ]
Li, Xiaolin [1 ,2 ]
Liu, Zhuang [1 ,2 ]
Utz, Paul J. [3 ]
Jiang, Kaili [4 ]
Fan, Shoushan [4 ]
Dai, Hongjie [1 ,2 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Stanford Univ, Adv Mat Lab, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[4] Tsinghua Univ, Dept Phys, Tsinghua Foxconn Nanotechnol Res Ctr, Beijing 100084, Peoples R China
基金
美国国家卫生研究院;
关键词
D O I
10.1038/nbt.1501
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The current sensitivity of standard fluorescence-based protein detection limits the use of protein arrays in research and clinical diagnosis. Here, we use functionalized, macromolecular single-walled carbon nanotubes ( SWNTs) as multicolor Raman labels for highly sensitive, multiplexed protein detection in an arrayed format. Unlike fluorescence methods, Raman detection benefits from the sharp scattering peaks of SWNTs with minimal background interference, affording a high signal-to-noise ratio needed for ultra-sensitive detection. When combined with surface-enhanced Raman scattering substrates, the strong Raman intensity of SWNT tags affords protein detection sensitivity in sandwich assays down to 1 fM-a three-order-of-magnitude improvement over most reports of fluorescence-based detection. We use SWNT Raman tags to detect human autoantibodies against proteinase 3, a biomarker for the autoimmune disease Wegener's granulomatosis, diluted up to 10(7)-fold in 1% human serum. SWNT Raman tags are not subject to photobleaching or quenching. By conjugating different antibodies to pure C-12 and C-13 SWNT isotopes, we demonstrate multiplexed two-color SWNT Raman- based protein detection.
引用
收藏
页码:1285 / 1292
页数:8
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