用于抗ccp超灵敏检测的超扁平、超洁净金纳米板

RAN Pub Date : 2017-04-01 DOI:10.11159/ICNB17.113
Eungwang Kim, H. Lee, Bongsoo Kim
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Anti-CCP is a highly specific biomarker (90%-95%) for RA, being in a very small quantity at early RA which does not show clinical symptoms.[3] Since it takes several months or even years to be characterized as RA from the chronic inflammation occurred at the synovial joints, the sensitivity is more important than detection time to identify the RA patients in early-stage. However, current sensors based on enzyme-linked immunosorbent assay (ELISA) methods have been focused on rapid detection of anti-CCPs. Recently, Dubacheva et al. reported super-selective targeting employing a well-defined self-assembled monolayer (SAM) formed on UV-ozone treated gold surface.[4] Because non-specific binding can cause false-positive signals and increase the zero-signal intensity, it is a key-factor which reduces the sensor’s sensitivity. Therefore, super-selective detection of the anti-CCPs by a well-defined CCP layer would play an important role in diagnosis of early RA. 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引用次数: 0

摘要

金在生物化学环境中非常稳定,可以通过Au-S键很容易地固定生物活性分子,包括dna、适体、抗体和肽。此外,金是一种优良的等离子体材料,已广泛用于制造敏感传感器。然而,金的内在表面缺陷,如台阶、台阶、空位和晶界,是实现生化分子完美固定化的主要问题。[1]因此,自上而下的抛光包括热退火、uv -臭氧清洗和羟基自由基蚀刻已被用于减少表面缺陷,但几乎不可能完全消除它们。[2]另一方面,在气相合成的金纳米片具有原子光滑的表面,没有任何表面缺陷,能够通过金属-分子界面的相干连接构建高度有序的生物分子层。高选择性检测抗环瓜氨酸肽(anti- ccp)已成为诊断早期类风湿关节炎(RA)的重要问题。Anti-CCP是一种高度特异性的RA生物标志物(90%-95%),在RA早期不表现临床症状时含量极低。[3]由于滑膜关节的慢性炎症需要数月甚至数年才能被诊断为RA,因此在早期识别RA患者时,灵敏度比检测时间更重要。然而,目前基于酶联免疫吸附测定(ELISA)方法的传感器主要集中在抗ccp的快速检测上。最近,Dubacheva等人报道了在uv -臭氧处理的金表面上形成的定义良好的自组装单层(SAM)的超选择性靶向。[4]非特异性结合会产生假阳性信号,增加零信号强度,是降低传感器灵敏度的关键因素。因此,通过明确的CCP层超选择性检测anti-CCP在早期RA的诊断中将发挥重要作用。表面增强拉曼散射(SERS)传感器由于其单分子水平的灵敏度而受到广泛关注。[5]在这里,我们报告了用超扁平、超净和单晶金纳米板制成的抗ccp SERS传感器,由于非特异性结合高度减少,与商业金膜相比,甚至可以检测到40 aM (0.1 pg/ml)的抗ccp。在金纳米片上有序排列的ccp可以明显增加目标信号,减少零信号,比现有SERS传感器的灵敏度提高100倍。此外,原子力显微镜(AFM)研究表明,在干燥环境下,金纳米板上形成了超灵敏的ccactive表面。因此,我们期望超扁平金纳米板SERS传感器能够实现抗ccp的原子摩尔检测,并将很好地用于RA的早期诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ultraflat, Ultraclean Au Nanoplate for Supersenstive Detection of Anti-CCPs
Extended Abstract Gold is very stable in biochemical environments and can immobilize easily bioactive molecules including DNAs, aptamers, antibodies, and peptides through Au-S bonding. In addition, gold is an excellent plasmonic material and has been widely used for fabrication of sensitive sensors. However, intrinsic surface defects of gold, such as step, terrace, vacancy, and grain boundary, are major problems for perfect immobilization of the biochemical molecules.[1] So, top-down polishing including thermal annealing, UV-ozone cleaning, and hydroxyl radical etching has been employed to reduce the surface defects, but being hardly possible to eliminate them completely.[2] On the other hand, Au nanoplates synthesized in vapor phase have atomically smooth surfaces without any surface defects, being able to construct a highly well-ordered bio-molecular layer from coherently linked metal-molecule interface. Highly-selective detection of anti-cyclic citrullinated peptides (anti-CCPs) has been an important issue to diagnose early rheumatoid arthritis (RA). Anti-CCP is a highly specific biomarker (90%-95%) for RA, being in a very small quantity at early RA which does not show clinical symptoms.[3] Since it takes several months or even years to be characterized as RA from the chronic inflammation occurred at the synovial joints, the sensitivity is more important than detection time to identify the RA patients in early-stage. However, current sensors based on enzyme-linked immunosorbent assay (ELISA) methods have been focused on rapid detection of anti-CCPs. Recently, Dubacheva et al. reported super-selective targeting employing a well-defined self-assembled monolayer (SAM) formed on UV-ozone treated gold surface.[4] Because non-specific binding can cause false-positive signals and increase the zero-signal intensity, it is a key-factor which reduces the sensor’s sensitivity. Therefore, super-selective detection of the anti-CCPs by a well-defined CCP layer would play an important role in diagnosis of early RA. Surface-Enhanced Raman Scattering (SERS) sensors employing hot spots by nanoscale gap between noble metal nanostructures have been much attention because of single molecule level sensitivity.[5] Here, we report that anti-CCP SERS sensor fabricated with ultraflat, ultraclean, and single-crystalline Au nanoplate can detect even 40 aM (0.1 pg/ml) of anti-CCPs due to highly reduced nonspecific bindings as 50 times compared to commercial Au film. The well-ordered CCPs on Au nanoplates can clearly increase target signals and decrease zero-signals, being able to improve the sensitivity as 100 times than current SERS sensor. Furthermore, atomic force microscopy (AFM) studies in dry ambient environment show distinctly the super-sensitive CCPactive surfaces formed on the Au nanoplate. Thus, we expect that ultraflat Au nanoplate SERS sensors enable attomolar detection of anti-CCPs and will be utilized excellently for early-diagnosis of RA.
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