...
首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Telomerase catalyzed fluorescent probes for sensitive protein profiling based on one-dimensional microfluidic beads array
【24h】

Telomerase catalyzed fluorescent probes for sensitive protein profiling based on one-dimensional microfluidic beads array

机译:基于一维微流控微珠阵列的端粒酶催化荧光探针用于敏感蛋白分析

获取原文
获取原文并翻译 | 示例

摘要

A nucleic acid-based signal amplified method for multiple proteins detection based on one-dimensional beads array using telomerase catalyzed fluorescent probes has been developed in this paper. The biotin labeled fluorescent probes were synthesized by telomerase in homogeneous solution. Approximately 360-480 fluorescein molecules were inserted in each probe. The limit of detection for p53 protein is 1.1 pM (S/N = 3) and a 3 orders of linear dynamic range is obtained. The sensitivity is nearly two orders higher than the two-site "sandwich" immunoassay using the same platform. Using this method, cellular p53 protein contents of as few as 85 CNE2 cells per mu l sample can be determined specifically. The expression changes of p53, c-myc and beta-actin in CNE2 cells were further examined as a function of anti-cancer drug treatment, and the results are consistent with our previous reports. Compared with immuno-polyrnerase chain reaction and immuno-rolling circle amplification, this method is simple, fast, cheap and suitable for multi-protein analysis. The multiplexed proteins profiling of cellular samples should facilitate the new opportunities to the fundamental research of tumor development and progression, especially to the low abundant tumor-associated proteins analysis. (c) 2008 Elsevier B.V. All rights reserved.
机译:本文开发了一种基于核酸的基于端粒酶催化的荧光探针的基于一维磁珠阵列的多种蛋白质检测信号放大方法。通过端粒酶在均质溶液中合成生物素标记的荧光探针。在每个探针中插入大约360-480个荧光素分子。 p53蛋白的检出限为1.1 pM(S / N = 3),并获得3个数量级的线性动态范围。灵敏度比使用同一平台的两点“三明治”免疫测定高近两个数量级。使用这种方法,可以特异性地确定每μl样品中少至85个CNE2细胞的细胞p53蛋白含量。进一步检查了CNE2细胞中p53,c-myc和β-肌动蛋白的表达变化与抗癌药物治疗的作用,结果与我们以前的报道一致。与免疫多聚酶链反应和免疫滚环扩增相比,该方法简便,快速,廉价,适用于多蛋白分析。细胞样品的多重蛋白谱分析应为肿瘤发展和进展的基础研究,特别是低丰度肿瘤相关蛋白分析提供新的机会。 (c)2008 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号