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非环(L)-苏糖醇核酸形成 i-发夹。

Formation of i-motifs from acyclic (l)-threoninol nucleic acids.

机构信息

Center for Multifunctional Biomolecular Drug Design (CEMBID), iNANO and Department of Chemistry, Aarhus University, 8000 Aarhus C, Denmark.

Department of Clinical Medicine - Research Unit for Molecular Medicine Aarhus University, 8200 Aarhus N, Denmark.

出版信息

Org Biomol Chem. 2019 Sep 7;17(33):7655-7659. doi: 10.1039/c9ob01220f. Epub 2019 Jul 30.

Abstract

Acyclic (l)-threoninol nucleic acids ((l)-aTNA) containing poly-cytosines are prepared and investigated at various pH values, revealing the formation of a highly stable structure at lower pH that have the characteristics of an i-motif. Depending on the sequence, the aTNA forms inter-, bi- and intra-molecular i-motif structures. Pyrene was conjugated to aTNA sequences and both monomeric and excimer fluorescence were efficiently quenched by the i-motif structures and thus demonstrated that the aTNA i-motif can serve as a pH switch.

摘要

含多胞嘧啶的非循环(L)-苏氨酸核酸((L)-aTNA)在不同 pH 值下进行制备和研究,在较低 pH 值下形成高度稳定的结构,具有 i-motif 的特征。根据序列的不同,aTNA 形成了分子间、分子内和分子内 i-motif 结构。将芘与 aTNA 序列缀合,并且 i-motif 结构有效地猝灭了单体和激基缔合物荧光,从而表明 aTNA i-motif 可以作为 pH 开关。

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