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Chemiluminescently labeled aptamers as the affinity probe for interaction analysis by capillary electrophoresis

机译:化学发光标记的适体作为亲和探针,用于通过毛细管电泳进行相互作用分析

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摘要

Aptamers are nucleic acid oligonucleotides, which can recognize targets with high affinity and specificity. Fluorescently labeled aptamers have been used as affinity probes in CE for interaction analysis. In this study, a method of labeling aptamers chemiluminescently with isoluminol isothiocyanate (ILITC) through covalent bonds was proposed and realized. The ILITC-labeled aptamers were characterized by HPLC-MS and purified by HPLC. After desalination, the ILITC-labeled aptamers were employed as the affinity probe for interaction analysis in CE coupled with chemiluminescence detection (CE-CL) by interface of end column reaction mode, the apparatus of which was home-designed and setup. CE-CL experiment conditions, including buffer pH, concentrations of horseradish peroxidase and H2O2, were optimized first. The system of thrombin and its 29-mer aptamer was chosen as the model. Binding parameters, namely the dissociation constant (Kd) and the binding site number (n), were calculated. The Kd obtained was 124.0±6.9 nM in agreement with the reported values. Thus, interaction analysis method based on chemiluminescently labeled aptamers as the affinity probe in CE-CL has been established. This method can be widely applied due to the ease and universality of the labeling method, simplicity of CE-CL apparatus and combination with aptamers for a wide range of targets.
机译:适体是核酸寡核苷酸,其可以高亲和力和特异性识别靶标。荧光标记的适体已在CE中用作亲和探针进行相互作用分析。在这项研究中,提出并实现了一种通过异戊醇异硫氰酸酯(ILITC)通过共价键化学发光标记适体的方法。通过HPLC-MS表征ILITC标记的适体,并通过HPLC纯化。脱盐后,通过末端柱反应模式的界面,将ILITC标记的适体用作亲和探针,用于CE中的相互作用分析以及化学发光检测(CE-CL),其装置是自行设计和设置的。首先优化了CE-CL的实验条件,包括缓冲液的pH值,辣根过氧化物酶的浓度和H 2 O 2 的浓度。选择凝血酶及其29聚体适体系统作为模型。计算了结合参数,即解离常数(K d )和结合位点数(n)。得到的K d 为124.0±6.9 nM,与报道值一致。因此,已经建立了基于化学发光标记的适体作为CE-CL中的亲和探针的相互作用分析方法。由于该标记方法的简便性和通用性,CE-CL设备的简便性以及与适用于多种靶标的适体的结合,因此该方法可以广泛应用。

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