Literature DB >> 28252182

Synthesis of Geranyl-2-Thiouridine-Modified RNA.

Rui Wang1, Phensinee Haruehanroengra1, Jia Sheng1.   

Abstract

This unit describes the chemical synthesis of the S-geranyl-2-thiouridine (ges2 U) phosphoramidite and its incorporation into RNA oligonucleotides through solid-phase synthesis. Starting from the 2-thiouracil nucleobase and the protected ribose, the 2-thiouridine is synthesized and the geranyl functionality is introduced into the 2-thio position by using geranyl bromide as the geranylating reagent before the conversion of this modified nucleoside into a phosphoramidite building block. The modified phosphoramidite is used to make the geranyl-RNA oligonucleotides with a solid-phase DNA synthesizer. These RNA strands are then purified by ion-exchange HPLC before further structural and functional studies, such as base pairing and enzyme recognition, can be done. © 2017 by John Wiley & Sons, Inc.
Copyright © 2017 John Wiley & Sons, Inc.

Entities:  

Keywords:  geranylation; natural RNA modification; nucleic acids; tRNA

Mesh:

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Year:  2017        PMID: 28252182     DOI: 10.1002/cpnc.22

Source DB:  PubMed          Journal:  Curr Protoc Nucleic Acid Chem        ISSN: 1934-9270


  1 in total

1.  Terpene Chain Length Affects the Base Pairing Discrimination of S-geranyl-2-thiouridine in RNA Duplex.

Authors:  Phensinee Haruehanroengra; Sweta Vangaveti; Srivathsan V Ranganathan; Song Mao; Max Daniel Su; Alan A Chen; Jia Sheng
Journal:  iScience       Date:  2020-11-26
  1 in total

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