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对自组装在电子束图案上的金纳米颗粒-免疫球蛋白G缀合物进行荧光生物识别。

Fluorescent biorecognition of gold nanoparticle-IgG conjugates self-assembled on E-beam patterns.

作者信息

Powell Tremaine, Yoon Jeong-Yeol

机构信息

Department of Agricultural and Biosystems Engineering, The University of Arizona, Tucson, Arizona 85721-0038, USA.

出版信息

Biotechnol Prog. 2006 Jan-Feb;22(1):106-10. doi: 10.1021/bp0501726.

Abstract

A new concept for line patterning of immunoglobulin G (IgG) in nanometer scale using gold nanoparticles (AuNPs) self-assembled in a nanochannel written with an electron beam is proposed and demonstrated. AuNPs are synthesized by reducing KAuCl4 with NaBH4, producing AuNPs 40-70 nm in size, where Cl- ions are capping AuNPs thus making them negatively charged and subsequently stabilized. IgG is conjugated to these AuNPs by simple adsorption. Single or multiple nanochannels are written with an electron beam using a scanning electron microscope (SEM) in a layer of poly(methyl methacrylate) (PMMA), which is spin-coated on a p-doped Si wafer. AuNPs bind into the etched nanochannel where the Si surface is exposed, while the relatively hydrophobic PMMA area repels the particles. The particles with a diameter larger than the channel width are not able to go inside of it. Anti-IgG, conjugated with fluorescein isothiocyanate (FITC), is then exposed to the patterned surface, binding specifically to the IgG-AuNP conjugates within the line patterns. These antibody-antigen bindings can be visualized with a fluorescent microscope, showing the fluorescent signal only along with the nanometer line pattern. These initial steps will lead to the formation of complex protein nanoarrays, based on the size-dependent self-assembly of AuNPs within variously sized nanopatterns.

摘要

提出并展示了一种利用在电子束写入的纳米通道中自组装的金纳米颗粒(AuNP)对免疫球蛋白G(IgG)进行纳米级线图案化的新概念。通过用硼氢化钠(NaBH4)还原氯金酸钾(KAuCl4)来合成AuNP,得到尺寸为40 - 70纳米的AuNP,其中氯离子包覆AuNP,使其带负电荷并随后稳定下来。通过简单吸附将IgG与这些AuNP偶联。使用扫描电子显微镜(SEM)在旋涂于p型掺杂硅晶片上的聚甲基丙烯酸甲酯(PMMA)层中用电子束写入单个或多个纳米通道。AuNP结合到蚀刻的纳米通道中,此处硅表面暴露,而相对疏水的PMMA区域排斥这些颗粒。直径大于通道宽度的颗粒无法进入通道内部。然后将与异硫氰酸荧光素(FITC)偶联的抗IgG暴露于图案化表面,使其特异性结合到线图案内的IgG - AuNP偶联物上。这些抗体 - 抗原结合可以用荧光显微镜观察到,仅沿纳米线图案显示荧光信号。基于不同尺寸纳米图案内AuNP的尺寸依赖性自组装,这些初始步骤将导致形成复杂的蛋白质纳米阵列。

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