4.4 Article

Practical Synthesis of Cap-4 RNA

期刊

CHEMBIOCHEM
卷 21, 期 1-2, 页码 265-271

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201900590

关键词

chemoenzymatic synthesis; oligonucleotides; mRNA caps; RNA modifications; solid-phase synthesis

资金

  1. Austrian Science Fund FWF [P27947, P31691]
  2. Austrian Research Promotion Agency FFG [West-Austrian BioNMR 858017]
  3. German Research Foundation DFG [SFB858]
  4. Austrian Science Fund (FWF) [P31691] Funding Source: Austrian Science Fund (FWF)

向作者/读者索取更多资源

Eukaryotic mRNAs possess 5 ' caps that are determinants for their function. A structural characteristic of 5 ' caps is methylation, with this feature already present in early eukaryotes such as Trypanosoma. While the common cap-0 (m(7)GpppN) shows a rather simple methylation pattern, the Trypanosoma cap-4 displays seven distinguished additional methylations within the first four nucleotides. The study of essential biological functions mediated by these unique structural features of the cap-4 and thereby of the metabolism of an important class of human pathogenic parasites is hindered by the lack of reliable preparation methods. Herein we describe the synthesis of custom-made nucleoside phosphoramidite building blocks for m(2)(6)Am and m(3)Um, their incorporation into short RNAs, the efficient construction of the 5 '-to-5 ' triphosphate bridge to guanosine by using a solid-phase approach, the selective enzymatic methylation at position N7 of the inverted guanosine, and enzymatic ligation to generate trypanosomatid mRNAs of up to 40 nucleotides in length. This study introduces a reliable synthetic strategy to the much-needed cap-4 RNA probes for integrated structural biology studies, using a combination of chemical and enzymatic steps.

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