RNA immunoprecipitation technique for Drosophila melanogaster S2 cells
- Authors: Kachaev Z.M.1, Gilmutdinov R.A.1, Kopytova D.V.1, Zheludkevich A.A.1, Shidlovskii Y.V.1, Kurbidaeva A.S.1
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Affiliations:
- Institute of Gene Biology
- Issue: Vol 51, No 1 (2017)
- Pages: 72-79
- Section: Molecular Cell Biology
- URL: https://journal-vniispk.ru/0026-8933/article/view/162933
- DOI: https://doi.org/10.1134/S002689331606008X
- ID: 162933
Cite item
Abstract
RNA-binding proteins play an important role in RNA metabolism, especially in mRNA biogenesis and subsequent expression patterns regulation. RNA immunoprecipitation (RIP) is a powerful tool for detecting protein–RNA associations. In this paper, we briefly cover the history of this method for analyzing RNA–protein interactions and reviewing a number of modifications of the RIP technique. We also present an adjusted RIP protocol that was modified for Drosophila S2 cell culture. The use of this protocol allows one to perform the efficient precipitation of RNA–protein complexes and harvest RNA in amounts that are sufficient for its downstream analysis.
About the authors
Z. M. Kachaev
Institute of Gene Biology
Author for correspondence.
Email: k-z-m@mail.ru
Russian Federation, Moscow, 119334
R. A. Gilmutdinov
Institute of Gene Biology
Email: k-z-m@mail.ru
Russian Federation, Moscow, 119334
D. V. Kopytova
Institute of Gene Biology
Email: k-z-m@mail.ru
Russian Federation, Moscow, 119334
A. A. Zheludkevich
Institute of Gene Biology
Email: k-z-m@mail.ru
Russian Federation, Moscow, 119334
Y. V. Shidlovskii
Institute of Gene Biology
Email: k-z-m@mail.ru
Russian Federation, Moscow, 119334
A. S. Kurbidaeva
Institute of Gene Biology
Email: k-z-m@mail.ru
Russian Federation, Moscow, 119334
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