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Titlebook: RNA‘Protein Interaction Protocols; Susan R. Haynes Book 19991st edition Humana Press 1999

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書(shū)目名稱RNA‘Protein Interaction Protocols
編輯Susan R. Haynes
視頻videohttp://file.papertrans.cn/821/820216/820216.mp4
叢書(shū)名稱Methods in Molecular Biology
圖書(shū)封面Titlebook: RNA‘Protein Interaction Protocols;  Susan R. Haynes Book 19991st edition Humana Press 1999
描述The molecular characterization of RNA and its interactions with proteins is an important and exciting area of current research. Organisms utilize a variety of RNA–protein interactions to regulate the expression of their genes. This is particularly true for eukaryotes, since newly synthesized messenger RNA must be extensively modified and transported to the cytoplasm before it can be used for protein synthesis. The realization that posttranscriptional processes are critical components of gene regulation has sparked an explosion of interest in both stable ribonucleoprotein (RNP) complexes and transient RNA–protein interactions. RNA is conformationally flexible and can adopt complex structures that provide diverse surfaces for interactions with proteins. The fact that short RNA molecules (aptamers; see Chapter 16) can be selected to bind many different types of molecules is evidence of the structural variability of RNA. RNA molecules are rarely entirely single- or double-stranded, but usually contain multiple short duplexes interrupted by single-stranded loops and bulges; in some RNAs, such as tRNAs, the short duplexes stack on each other. Further variability is generated by the prese
出版日期Book 19991st edition
版次1
doihttps://doi.org/10.1385/1592596762
isbn_ebook978-1-59259-676-8Series ISSN 1064-3745 Series E-ISSN 1940-6029
issn_series 1064-3745
copyrightHumana Press 1999
The information of publication is updating

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An ,-Based Genetic Strategy for Characterizing RNA Binding Proteins, have simplified the analysis of RNA-protein interactions. Nevertheless, a thorough analysis of an RNA-BP is not a trivial task, and, at present, there are only a few RNA-BPs that have been characterized in detail.
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In Vitro Genetic Analysis of RNA-Binding Proteins Using Phage Display,NA. To gain more insight into RNA-protein interaction, several genetic systems have been developed in the last few years (.–.) (.. and .). The system described in this chapter is based on in vitro genetics. This means that the selective step (in this case, the binding of an RNA-BP to RNA) occurs outside of a living organism, in the test tube.
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Book 19991st editionriety of RNA–protein interactions to regulate the expression of their genes. This is particularly true for eukaryotes, since newly synthesized messenger RNA must be extensively modified and transported to the cytoplasm before it can be used for protein synthesis. The realization that posttranscripti
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Labeling and Purification of RNA Synthesized by In Vitro Transcription,vitro (.–.). Early methods of in vitro transcription included the use of eukary-otic cell extracts or . RNA polymerase to transcribe DNA templates containing the appropriate promoter. Ideally, however, the optimal in vitro transcription system should require simple buffer components without need for
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The Methylene Blue Mediated Photocrosslinking Method for Dectection of Proteins that Interact with lves illuminating a mixture of protein and nucleic acid with light of a suitable wavelength to induce photochemical reactions that result in covalent linkages between the nucleic acid and the protein. The protein can be a purified or a recombinant RNA binding protein, but perhaps a more common appli
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