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迈向血清中单个病毒颗粒的检测。

Toward the detection of single virus particle in serum.

作者信息

Zhang Yuexing, Bahns John T, Jin Qiaoling, Divan Ralu, Chen Liaohai

机构信息

Biosciences Division, Argonne National Laboratory, Argonne, IL 60439, USA.

出版信息

Anal Biochem. 2006 Sep 15;356(2):161-70. doi: 10.1016/j.ab.2006.06.036. Epub 2006 Jul 31.

Abstract

There is a grand challenge for the detection of target molecules at single molecule sensitivity in a bulk body fluid for the early diagnosis of diseases. We report our progress on tackling this challenge via the combination of fluorescence cross-correlation spectroscopy (FCCS) and micro fabricated devices toward highly sensitive detection of the dengue virus. We demonstrate that by using a dengue-specific antibody, we can probe the individual dengue virus in a nanomolar bulk solution by following the specific association of dengue antibody using FCCS. Consequently, we designed and fabricated a microfluidic chamber array structure and were able to compartmentalize the bulk aqueous dengue sample into femtoliter volumes using such a device. More importantly we demonstrate that we can differentiate between the compartments containing the dengue virus and the virus-free compartments. Our experiment suggests that by expanding the throughput using microfluidic devices integrated with FCCS, both of which can be achieved practically, we should be able to detect single virus particle in human body fluids in the near future.

摘要

在体液中以单分子灵敏度检测目标分子以实现疾病的早期诊断面临着巨大挑战。我们报告了通过荧光互相关光谱法(FCCS)与微制造器件相结合来应对这一挑战以实现对登革热病毒的高灵敏度检测方面取得的进展。我们证明,通过使用登革热特异性抗体,利用FCCS追踪登革热抗体的特异性结合,我们能够在纳摩尔浓度的体液溶液中探测单个登革热病毒。因此,我们设计并制造了一种微流控腔阵列结构,并且能够使用这样的器件将大量水性登革热样本分隔成飞升体积。更重要的是,我们证明了我们能够区分含有登革热病毒的隔室和不含病毒的隔室。我们的实验表明,通过使用与FCCS集成的微流控器件来提高通量,这两者在实际中都可以实现,我们在不久的将来应该能够在人体体液中检测到单个病毒颗粒。

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