{"title":"Salt","authors":"C. Adams","doi":"10.2307/j.ctt22nmcfb.9","DOIUrl":null,"url":null,"abstract":"Conventional solid-state nanopore measurements sense all translocating entities, necessitating meticulous analysis to differentiate target biomolecules. To address this, we have established a selective assay with the platform that has shown utility in quantifying several nucleic acid biomarkers. However, limited detection efficiency and intrinsic noise have so far limited assay resolution to 10 nM. Improvements in this value require manipulation of translocation dynamics. Here, we report the effects of NaCl conditions on assay performance. We first investigate symmetric conditions, finding sensitivity increases with salt concentration but selectivity is maximized at 1.0 M NaCl. We then probe asymmetric conditions, showing a remarkable impact on assay sensitivity and selectivity when measurement buffer NaCl concentration in the reservoir with the translocating molecules is low and the opposite reservoir is increased. Using optimum conditions, we demonstrate detection of target biomolecules down to a concentration of 100 pM which is an improvement of 2 orders of magnitude over past results.","PeriodicalId":335024,"journal":{"name":"Encyclopedia of Cryptography, Security and Privacy","volume":"134 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2018-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Encyclopedia of Cryptography, Security and Privacy","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2307/j.ctt22nmcfb.9","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Conventional solid-state nanopore measurements sense all translocating entities, necessitating meticulous analysis to differentiate target biomolecules. To address this, we have established a selective assay with the platform that has shown utility in quantifying several nucleic acid biomarkers. However, limited detection efficiency and intrinsic noise have so far limited assay resolution to 10 nM. Improvements in this value require manipulation of translocation dynamics. Here, we report the effects of NaCl conditions on assay performance. We first investigate symmetric conditions, finding sensitivity increases with salt concentration but selectivity is maximized at 1.0 M NaCl. We then probe asymmetric conditions, showing a remarkable impact on assay sensitivity and selectivity when measurement buffer NaCl concentration in the reservoir with the translocating molecules is low and the opposite reservoir is increased. Using optimum conditions, we demonstrate detection of target biomolecules down to a concentration of 100 pM which is an improvement of 2 orders of magnitude over past results.
传统的固态纳米孔测量方法可以感知所有移位的实体,需要细致的分析来区分目标生物分子。为了解决这个问题,我们已经建立了一个选择性的分析与平台,已显示出量化几种核酸生物标志物的效用。然而,有限的检测效率和固有噪声迄今为止将分析分辨率限制在10 nM。这个值的改进需要对移位动力学进行操作。在这里,我们报告了NaCl条件对测定性能的影响。我们首先研究了对称条件,发现灵敏度随盐浓度的增加而增加,但在1.0 M NaCl时选择性最大。然后,我们探索了不对称条件,当测量具有易位分子的储层中缓冲NaCl浓度较低而相反的储层增加时,对分析灵敏度和选择性有显著影响。使用最佳条件,我们演示了目标生物分子的检测低至100 pM的浓度,这比过去的结果提高了2个数量级。