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立体规整的寡聚(核苷硫代磷酸酯)在人血浆中的稳定性:血浆3'-外切核酸酶的非对映选择性

Stability of stereoregular oligo(nucleoside phosphorothioate)s in human plasma: diastereoselectivity of plasma 3'-exonuclease.

作者信息

Koziołkiewicz M, Wójcik M, Kobylańska A, Karwowski B, Rebowska B, Guga P, Stec W J

机构信息

Polish Academy of Sciences, Department of Bioorganic Chemistry, Lódź, Poland.

出版信息

Antisense Nucleic Acid Drug Dev. 1997 Feb;7(1):43-8. doi: 10.1089/oli.1.1997.7.43.

Abstract

The stability of stereoregular oligo(nucleoside phosphorothioate)s (PS-oligos) in human plasma has been studied. 3'-Exonuclease present in human plasma appeared to be RP specific, that is, it cleaves internucleotide phosphorothioate linkages of [RP]-configuration and not those of [SP]-configuration. Therefore, PS-oligos containing all phosphorothioate internucleotide linkages of [RP]-configuration [RP-PS-oligos]) are more effectively degraded by the enzyme than PS-oligos prepared via nonstereo-controlled methods (so-called random mixture of diastereomers [Mix-PS-oligos]), whereas oligo(nucleoside phosphorothioate)s of [S(P)]-configuration remain intact. The enzyme activity depends on the sequence of nucleobases. The presence of deoxycytidine units (three or more residues) at the 3'-end of PS-oligo substrate significantly inhibits the enzyme activity.

摘要

已经对立体规整的寡聚(核苷硫代磷酸酯)(PS-寡聚物)在人血浆中的稳定性进行了研究。人血浆中存在的3'-外切核酸酶似乎对RP具有特异性,也就是说,它能切割[RP]构型的核苷酸间硫代磷酸酯键,而不能切割[SP]构型的键。因此,与通过非立体控制方法制备的PS-寡聚物(所谓的非对映异构体随机混合物[Mix-PS-寡聚物])相比,含有所有[RP]构型的核苷酸间硫代磷酸酯键的PS-寡聚物[RP-PS-寡聚物])被该酶更有效地降解,而[S(P)]构型的寡聚(核苷硫代磷酸酯)则保持完整。酶活性取决于核碱基的序列。PS-寡聚物底物3'-末端存在脱氧胞苷单元(三个或更多残基)会显著抑制酶活性。

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