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RNA affinity tags for the rapid purification and investigation of RNAs and RNA-protein complexes

  • University of Michigan Medical School

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

32 Citations (Scopus)

Abstract

Isolation of ribonucleoprotein particles from living cells and cell lysates has allowed the identification of both simple bimolecular interactions and the members of large, extended complexes. A number of different strategies have been devised to isolate these complexes by using affinity purification methods that are specific for the RNA rather than the protein components of these complexes. We describe the use of two such RNA affinity tags: small RNAs that bind with high affinity and specificity to either Sephadex beads or streptavidin affinity resins and can be eluted under mild, native conditions that retain intact complexes. The tags can be inserted into appropriate locations in genes encoding the RNA components, and ribonucleoproteins can be assembled either in vivo or in vitro before affinity isolation. Strategies toward the design and production of these tagged RNA sequences are discussed, and the purification procedure is outlined.

Original languageEnglish
Title of host publicationRNA-Protein Interaction Protocols
PublisherHumana Press
Pages23-40
Number of pages18
ISBN (Print)9781588294197
DOIs
Publication statusPublished - 2008

Publication series

NameMethods in Molecular Biology
Volume488
ISSN (Print)1064-3745

Keywords

  • Aptamer
  • RNA
  • RNP isolation
  • Ribonucleoprotein
  • SELEX
  • Sephadex
  • Streptavidin

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