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使用无标记电化学方法检测凝血酶结合适体的折叠

Detection for folding of the thrombin binding aptamer using label-free electrochemical methods.

作者信息

Cho Minseon, Kim Yeonwha, Han Se-Young, Min Kyungin, Rahman Md Aminur, Shim Yoon-Bo, Ban Changill

机构信息

Department of Chemistry, Pohang University of Science and Technology, Pohang, Korea.

出版信息

BMB Rep. 2008 Feb 29;41(2):126-31. doi: 10.5483/bmbrep.2008.41.2.126.

Abstract

The folding of aptamer immobilized on an Au electrode was successfully detected using label-free electrochemical methods. A thrombin binding DNA aptamer was used as a model system in the presence of various monovalent cations. Impedance spectra showed that the extent to which monovalent cations assist in folding of aptamer is ordered as K(+) > NH(4)(+) > Na(+) > Cs(+). Our XPS analysis also showed that K(+) and NH(4)(+) caused a conformational change of the aptamer in which it forms a stable complex with these monovalent ions. Impedance results for the interaction between aptamer and thrombin indicated that thrombin interacts more with folded aptamer than with unfolded aptamer. The EQCM technique provided a quantitative analysis of these results. In particular, the present impedance results showed that thrombin participates a folding of aptamer to some extent, and XPS analysis confirmed that thrombin stabilizes and induces the folding of aptamer.

摘要

利用无标记电化学方法成功检测了固定在金电极上的适体的折叠情况。在各种单价阳离子存在的情况下,使用凝血酶结合DNA适体作为模型系统。阻抗谱表明,单价阳离子协助适体折叠的程度顺序为K(+) > NH(4)(+) > Na(+) > Cs(+)。我们的XPS分析还表明,K(+)和NH(4)(+)导致适体构象发生变化,使其与这些单价离子形成稳定的复合物。适体与凝血酶相互作用的阻抗结果表明,凝血酶与折叠后的适体相互作用比与未折叠的适体更强。EQCM技术对这些结果进行了定量分析。特别是,目前的阻抗结果表明,凝血酶在一定程度上参与了适体的折叠,XPS分析证实凝血酶稳定并诱导了适体的折叠。

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