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RNA Remodeling Proteins

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Cover of 'RNA Remodeling Proteins'

Table of Contents

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    Book Overview
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    Chapter 1 Key Points to Consider When Studying RNA Remodeling by Proteins
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    Chapter 2 Happy Birthday: 25 Years of DEAD-Box Proteins.
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    Chapter 3 In Vivo Cross-Linking Followed by PolyA Enrichment to Identify Yeast mRNA Binding Proteins.
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    Chapter 4 Dynamics of the spb4 interactome monitored by affinity purification.
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    Chapter 5 Using EMOTE to Map the Exact 5′-Ends of Processed RNA on a Transcriptome-Wide Scale
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    Chapter 6 Cellular Localization of RNA Degradation and Processing Components in Escherichia coli
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    Chapter 7 Recombineering Applications for the Mutational Analysis of Bacterial RNA-Binding Proteins and Their Sites of Action
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    Chapter 8 Determination of RNA Chaperone Activity Using an Escherichia coli Mutant
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    Chapter 9 Biochemical Characterization of G4 Quadruplex Telomerase RNA Unwinding by the RNA Helicase RHAU
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    Chapter 10 ATPase Site Configuration of the RNA Helicase DbpA Probed by ENDOR Spectroscopy
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    Chapter 11 Bioinformatics and Biochemical Methods to Study the Structural and Functional Elements of DEAD-Box RNA Helicases
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    Chapter 12 Measuring Helicase Inhibition of the DEAD-Box Protein Dbp2 by Yra1.
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    Chapter 13 A FRET-Based, Continuous Assay for the Helicase Activity of DEAD-Box Proteins
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    Chapter 14 A Fluorescence-Based Screening Assay for Identification of Hepatitis C Virus NS3 Helicase Inhibitors and Characterization of Their Inhibitory Mechanism
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    Chapter 15 Mechanisms of HCV NS3 Helicase Monitored by Optical Tweezers
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    Chapter 16 Constructing a Magnetic Tweezers to Monitor RNA Translocation at the Single-Molecule Level
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    Chapter 17 Probing RNA Translocases with DNA
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    Chapter 18 Monitoring RNA Unwinding by the Transcription Termination Factor Rho from Mycobacterium tuberculosis
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    Chapter 19 Characterization of the mechanisms of transcription termination by the helicase sen1.
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    Chapter 20 Characterization of TRAP-Mediated Regulation of the B. subtilis trp Operon Using In Vitro Transcription and Transcriptional Reporter Fusions In Vivo
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    Chapter 21 Single-Molecule FRET Characterization of RNA Remodeling Induced by an Antitermination Protein
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    Chapter 22 Fluorescence Reporters for Hfq Oligomerization and RNA Annealing
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    Chapter 23 Fluorescence anisotropy-based salt-titration approach to characterize protein-nucleic Acid interactions.
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    Chapter 24 Probing Hfq:RNA Interactions with Hydroxyl Radical and RNase Footprinting.
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    Chapter 25 Purification of Eukaryotic Exoribonucleases Following Heterologous Expression in Bacteria and Analysis of Their Biochemical Properties by In Vitro Enzymatic Assays
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    Chapter 26 Tips and Tricks to Probe the RNA-Degrading Activities of Hyperthermophilic Archaeal β-CASP Ribonucleases.
Attention for Chapter 26: Tips and Tricks to Probe the RNA-Degrading Activities of Hyperthermophilic Archaeal β-CASP Ribonucleases.
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Chapter title
Tips and Tricks to Probe the RNA-Degrading Activities of Hyperthermophilic Archaeal β-CASP Ribonucleases.
Chapter number 26
Book title
RNA Remodeling Proteins
Published in
Methods in molecular biology, January 2015
DOI 10.1007/978-1-4939-2214-7_26
Pubmed ID
Book ISBNs
978-1-4939-2213-0, 978-1-4939-2214-7
Authors

Phung DK, Clouet-d'Orval B, Duy Khanh Phung, Béatrice Clouet-d’Orval

Abstract

The importance of ribonucleases in posttranscriptional control of gene expression has been established in Eukarya and Bacteria for over a decade. However, this process has been overlooked in Archaea, which are of universal importance to elucidate fundamental biological mechanisms and to study the evolution of life on Earth. Very few ribonucleolytic activities have been reported in Archaea, and RNA metabolism pathways wait to be described. Recently we have identified two major groups of archaeal ribonucleases, aCPSF1 and aRNase J, which are members of the β-CASP metallo-β-lactamase family. Here, we describe in vitro methods to characterize the endo- and exoribonucleolytic activities of hyperthermophilic archaeal β-CASP ribonucleases. The use of various labeled RNA substrates allows defining the specificity of RNA cleavage and the directionality of the exoribonucleolytic trimming activity of the archaeal enzymes which work at high temperature. Elucidating in vitro ribonucleolytic activities is one step toward the understanding of the role of β-CASP ribonucleases in RNA metabolism pathways in archaeal cells.

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Mendeley readers

The data shown below were compiled from readership statistics for 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Bachelor 1 17%
Professor 1 17%
Professor > Associate Professor 1 17%
Researcher 1 17%
Unknown 2 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 50%
Agricultural and Biological Sciences 1 17%
Unknown 2 33%