首页> 外文期刊>Journal of the American Chemical Society >Endonuclease-Based Logic Gates and Sensors Using Magnetic Force-Amplified Readout of DNA Scission on Cantilevers
【24h】

Endonuclease-Based Logic Gates and Sensors Using Magnetic Force-Amplified Readout of DNA Scission on Cantilevers

机译:基于核酸内切酶的逻辑门和传感器,利用磁力放大的悬臂DNA断裂信息

获取原文
获取原文并翻译 | 示例
       

摘要

The endonuclease scission of magnetic particles functionalized with sequence-specific DNAs, which are associated on cantilevers, is followed by the magnetic force-amplified readout of the reactions by the nano-mechanical deflection/retraction of the cantilevers. The systems are employed to develop AND or OR logic gates and to detect single base mismatch specificity of the endonucleases. The two endonucleases EcoRI (E_A) and Ascl (E_B) are used as inputs. The removal of magnetic particles linked to the cantilever by the duplexes 1/1a and 2/2a via the simultaneous cleavage of the DNAs by E_A and E_B leads to the retraction of the magnetically deflected cantilever and to the establishment of the "AND" gate. The removal of the magnetic particles linked to the cantilevers by the duplex 3/3a by either E_A or E_B leads to the retraction of the magnetically deflected cantilever and to the establishment of the "OR" gate. The magnetic force-amplified readout of endonuclease activities is also employed to reveal single base mismatch specificity of the biocatalysts.
机译:在悬臂上关联被序列特异性DNA功能化的磁性粒子的核酸内切酶裂解,随后通过悬臂的纳米机械偏转/收缩磁力放大反应的读数。该系统用于开发“或”或“或”逻辑门,并检测核酸内切酶的单碱基错配特异性。两种核酸内切酶EcoRI(E_A)和Ascl(E_B)用作输入。通过E_A和E_B同时切割DNA,通过双链体1 / 1a和2 / 2a连接到悬臂的磁性颗粒的去除导致磁偏转的悬臂的缩回和“与”门的建立。通过E_A或E_B去除通过双链体3 / 3a连接到悬臂的磁性颗粒导致磁偏转的悬臂的缩回和“或”门的建立。核酸内切酶活性的磁力放大读数也用于揭示生物催化剂的单碱基错配特异性。

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