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Histones

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Cover of 'Histones'

Table of Contents

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    Book Overview
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    Chapter 1 In Vitro Assembly of Nucleosomes for Binding/Remodeling Assays.
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    Chapter 2 An Assay for Measuring Histone Variant Exchange within Nucleosomes In Vitro.
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    Chapter 3 Purification of Yeast Native Reagents for the Analysis of Chromatin Function-I: Nucleosomes for Reconstitution and Manipulation of Histone Marks.
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    Chapter 4 Purification of Yeast Native Reagents for the Analysis of Chromatin Function-II: Multiprotein Complexes and Biochemical Assays.
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    Chapter 5 Histone Purification from Saccharomyces cerevisiae.
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    Chapter 6 Analytical Ultracentrifuge Analysis of Nucleosomes Assembled from Recombinant, Acid-Extracted, HPLC-Purified Histones.
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    Chapter 7 SILAC-Based Quantitative Strategies for Accurate Histone Posttranslational Modification Profiling Across Multiple Biological Samples.
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    Chapter 8 Characterization of Individual Histone Posttranslational Modifications and Their Combinatorial Patterns by Mass Spectrometry-Based Proteomics Strategies.
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    Chapter 9 Production and Purification of Antibodies Against Histone Modifications.
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    Chapter 10 Immunofluorescence of Histone Proteins.
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    Chapter 11 Acid-Urea Gel Electrophoresis and Western Blotting of Histones.
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    Chapter 12 Chromatin Immunoprecipitation of Histone Modifications in Fission Yeast.
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    Chapter 13 A Spiking Strategy for ChIP-chip Data Normalization in S. cerevisiae.
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    Chapter 14 High-Resolution Genome-Wide Mapping of Nucleosome Positioning and Occupancy Level Using Paired-End Sequencing Technology.
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    Chapter 15 Physarum polycephalum for Studying the Function of Histone Modifications In Vivo.
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    Chapter 16 A Method for Large-Scale Screening of Random Sequence Libraries to Determine the Function of Unstructured Regions from Essential Proteins.
Attention for Chapter 16: A Method for Large-Scale Screening of Random Sequence Libraries to Determine the Function of Unstructured Regions from Essential Proteins.
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Chapter title
A Method for Large-Scale Screening of Random Sequence Libraries to Determine the Function of Unstructured Regions from Essential Proteins.
Chapter number 16
Book title
Histones
Published in
Methods in molecular biology, January 2017
DOI 10.1007/978-1-4939-6630-1_16
Pubmed ID
Book ISBNs
978-1-4939-6628-8, 978-1-4939-6630-1
Authors

Jean-François Millau, Benoit Guillemette, Luc Gaudreau

Editors

Benoit Guillemette, Luc R. Gaudreau

Abstract

In this chapter we present a method allowing the screening of random sequences to discover essential aspects of unstructured protein regions in yeast. The approach can be applied to any protein with unstructured peptide sequences for which functions are difficult to decipher, for example the N-terminal tails of histones. The protocol first describes the building and preparation of a large library of random peptides in fusion with a protein of interest. Recent technical advances in oligonucleotide synthesis allow the construction of long random sequences up to 35 residues long. The protocol details the screening of the library in yeast for sequences that can functionally replace an unstructured domain in an essential protein in vivo. Our method typically identifies sequences that, while being totally different from the wild type, retain essential features allowing yeast to live. This collection of proteins with functional synthetic sequences can subsequently be used in phenotypic tests or genetic screens in order to discover genetic interaction.

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Mendeley readers

The data shown below were compiled from readership statistics for 5 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 5 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 3 60%
Student > Ph. D. Student 1 20%
Librarian 1 20%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 40%
Biochemistry, Genetics and Molecular Biology 2 40%
Arts and Humanities 1 20%