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利用DNA纳米结构生物传感器和多分支杂交链式反应扩增技术对癌细胞进行多价捕获与检测。

Multivalent capture and detection of cancer cells with DNA nanostructured biosensors and multibranched hybridization chain reaction amplification.

作者信息

Zhou Guobao, Lin Meihua, Song Ping, Chen Xiaoqing, Chao Jie, Wang Lianhui, Huang Qing, Huang Wei, Fan Chunhai, Zuo Xiaolei

机构信息

Division of Physical Biology & Bioimaging Center, Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences , Shanghai, China 201800.

出版信息

Anal Chem. 2014 Aug 5;86(15):7843-8. doi: 10.1021/ac502276w. Epub 2014 Jul 14.

Abstract

Sensitive detection of cancer cells plays a critically important role in the early detection of cancer and cancer metastasis. However, because circulating tumor cells are extremely rare in peripheral blood, the detection of cancer cells with high analytical sensitivity and specificity remains challenging. Here, we have demonstrated a simple, sensitive and specific detection of cancer cells with the detection sensitivity of four cancer cells, which is lower than the cutoff value with respect to correlation with survival outcomes as well as predictive of metastatic disease in clinical diagnostics. We re-engineered the hybridization chain reaction (HCR) to multibranched HCR (mHCR) that can produce long products with multiple biotins for signal amplification and multiple branched arms for multivalent binding. The capturing gold surface is modified with DNA tetrahedral probes, which provide superior hybridization conditions for the multivalent binding. The synergetic effect of mHCR amplification and multivalent binding lead to the high sensitivity of our detection platform.

摘要

癌细胞的灵敏检测在癌症早期检测及癌症转移方面起着至关重要的作用。然而,由于循环肿瘤细胞在外周血中极其罕见,以高分析灵敏度和特异性检测癌细胞仍然具有挑战性。在此,我们展示了一种简单、灵敏且特异的癌细胞检测方法,其检测灵敏度可达四个癌细胞,这一灵敏度低于与生存结果相关以及在临床诊断中预测转移性疾病的临界值。我们将杂交链式反应(HCR)重新设计为多分支HCR(mHCR),它能够产生带有多个生物素的长产物用于信号放大,以及多个分支臂用于多价结合。捕获金表面用DNA四面体探针进行修饰,为多价结合提供了优越的杂交条件。mHCR扩增和多价结合的协同效应导致了我们检测平台的高灵敏度。

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