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Bacterial Regulatory RNA

Overview of attention for book
Cover of 'Bacterial Regulatory RNA'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Workflow for a Computational Analysis of an sRNA Candidate in Bacteria
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    Chapter 2 Guidelines for Inferring and Characterizing a Family of Bacterial trans-Acting Small Noncoding RNAs
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    Chapter 3 Bioinformatic Approach for Prediction of CsrA/RsmA-Regulating Small RNAs in Bacteria
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    Chapter 4 Host-Pathogen Transcriptomics by Dual RNA-Seq
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    Chapter 5 Identification of New Bacterial Small RNA Targets Using MS2 Affinity Purification Coupled to RNA Sequencing
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    Chapter 6 Assessment of External Guide Sequences’ (EGS) Efficiency as Inducers of RNase P-Mediated Cleavage of mRNA Target Molecules
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    Chapter 7 Evaluating the Effect of Small RNAs and Associated Chaperones on Rho-Dependent Termination of Transcription In Vitro
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    Chapter 8 Mapping Changes in Cell Surface Protein Expression Through Selective Labeling of Live Cells
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    Chapter 9 Fluorescence-Based Methods for Characterizing RNA Interactions In Vivo
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    Chapter 10 Mutational Analysis of sRNA–mRNA Base Pairing by Electrophoretic Mobility Shift Assay
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    Chapter 11 An Integrated Cell-Free Assay to Study Translation Regulation by Small Bacterial Noncoding RNAs
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    Chapter 12 Quantitative Super-Resolution Imaging of Small RNAs in Bacterial Cells
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    Chapter 13 Extraction and Analysis of RNA Isolated from Pure Bacteria-Derived Outer Membrane Vesicles
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    Chapter 14 Absolute Regulatory Small Noncoding RNA Concentration and Decay Rates Measurements in Escherichia coli
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    Chapter 15 High-Resolution, High-Throughput Analysis of Hfq-Binding Sites Using UV Crosslinking and Analysis of cDNA (CRAC)
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    Chapter 16 Producing Hfq/Sm Proteins and sRNAs for Structural and Biophysical Studies of Ribonucleoprotein Assembly
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    Chapter 17 Single-Molecule FRET Assay to Observe the Activity of Proteins Involved in RNA/RNA Annealing
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    Chapter 18 Techniques to Analyze sRNA Protein Cofactor Self-Assembly In Vitro
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    Chapter 19 Sequence-Specific Affinity Chromatography of Bacterial Small Regulatory RNA-Binding Proteins from Bacterial Cells
  21. Altmetric Badge
    Chapter 20 Identification of Small RNA–Protein Partners in Plant Symbiotic Bacteria
  22. Altmetric Badge
    Chapter 21 A Modular Genetic System for High-Throughput Profiling and Engineering of Multi-Target Small RNAs
Attention for Chapter 13: Extraction and Analysis of RNA Isolated from Pure Bacteria-Derived Outer Membrane Vesicles
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Chapter title
Extraction and Analysis of RNA Isolated from Pure Bacteria-Derived Outer Membrane Vesicles
Chapter number 13
Book title
Bacterial Regulatory RNA
Published in
Methods in molecular biology, January 2018
DOI 10.1007/978-1-4939-7634-8_13
Pubmed ID
Book ISBNs
978-1-4939-7633-1, 978-1-4939-7634-8
Authors

Janine Habier, Patrick May, Anna Heintz-Buschart, Anubrata Ghosal, Anke K. Wienecke-Baldacchino, Esther N. M. Nolte-‘t Hoen, Paul Wilmes, Joëlle V. Fritz, Habier, Janine, May, Patrick, Heintz-Buschart, Anna, Ghosal, Anubrata, Wienecke-Baldacchino, Anke K., Nolte-‘t Hoen, Esther N. M., Wilmes, Paul, Fritz, Joëlle V.

Abstract

Outer membrane vesicles (OMVs) are released by commensal as well as pathogenic Gram-negative bacteria. These vesicles contain numerous bacterial components, such as proteins, peptidoglycans, lipopolysaccharides, DNA, and RNA. To examine if OMV-associated RNA molecules are bacterial degradation products and/or are functionally active, it is necessary to extract RNA from pure OMVs for subsequent analysis. Therefore, we describe here an isolation method of ultrapure OMVs and the subsequent extraction of RNA and basic steps of RNA-Seq analysis. Bacterial culture, extracellular supernatant concentration, OMV purification, and the subsequent RNA extraction out of OMVs are described. Specific pitfalls within the protocol and RNA contamination sources are highlighted.

X Demographics

X Demographics

The data shown below were collected from the profiles of 5 X users who shared this research output. Click here to find out more about how the information was compiled.
Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 22 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 22 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 3 14%
Researcher 3 14%
Student > Ph. D. Student 2 9%
Student > Master 2 9%
Student > Bachelor 1 5%
Other 1 5%
Unknown 10 45%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 4 18%
Agricultural and Biological Sciences 2 9%
Environmental Science 1 5%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Immunology and Microbiology 1 5%
Other 2 9%
Unknown 11 50%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 3. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 14 March 2018.
All research outputs
#15,232,080
of 26,017,215 outputs
Outputs from Methods in molecular biology
#4,019
of 14,458 outputs
Outputs of similar age
#232,473
of 455,808 outputs
Outputs of similar age from Methods in molecular biology
#309
of 1,490 outputs
Altmetric has tracked 26,017,215 research outputs across all sources so far. This one is in the 40th percentile – i.e., 40% of other outputs scored the same or lower than it.
So far Altmetric has tracked 14,458 research outputs from this source. They receive a mean Attention Score of 3.5. This one has gotten more attention than average, scoring higher than 71% of its peers.
Older research outputs will score higher simply because they've had more time to accumulate mentions. To account for age we can compare this Altmetric Attention Score to the 455,808 tracked outputs that were published within six weeks on either side of this one in any source. This one is in the 48th percentile – i.e., 48% of its contemporaries scored the same or lower than it.
We're also able to compare this research output to 1,490 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 77% of its contemporaries.