Detection of 3′-End RNA Uridylation with a Protein Nanopore

被引:29
作者
Clamer, Massimiliano [1 ,2 ]
Hoefler, Lajos [1 ]
Mikhailova, Ellina [1 ]
Viero, Gabriella [2 ,3 ]
Bayley, Hagan [1 ]
机构
[1] Univ Oxford, Dept Chem, Oxford OX1 3TA, England
[2] Univ Trento, Lab Translat Genom, Ctr Integrat Biol, I-38123 Mattarello, TN, Italy
[3] CNR, Inst Biophys, I-38123 Povo, Trento, Italy
基金
美国国家卫生研究院;
关键词
RNA; post-transcriptional modification; nanopore; alpha-hemolysin; RNA sensor; untranslated regions; BASE-RECOGNITION; ALPHA-HEMOLYSIN; STRANDED-RNA; SM CORE; MOLECULES; BINDING; DISCRIMINATION; ACID; OLIGONUCLEOTIDES; POLYURIDYLATION;
D O I
10.1021/nn4050479
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Post-transcriptional modifications of the 3'-ends of RNA molecules have a profound impact on their stability and processing in the cell. Uridylation, the addition of uridines to 3'-ends, has recently been found to be an important regulatory signal to stabilize the tagged molecules or to direct them toward degradation. Simple and cost-effective methods for the detection of this post-transcriptional modification are not yet available. Here, we demonstrate the selective and transient binding of 3'-uridylated ssRNAs inside the beta barrel of the staphylococcal a-hemolysin (aHL) nanopore and investigate the molecular basis of uridine recognition by the pore. We show the discrimination of 3'-oligouridine tails on the basis of their lengths and propose the aHL nanopore as a useful sensor for this biologically relevant RNA modification.
引用
收藏
页码:1364 / 1374
页数:11
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