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Intrinsically Disordered Protein Analysis

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Cover of 'Intrinsically Disordered Protein Analysis'

Table of Contents

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    Book Overview
  2. Altmetric Badge
    Chapter 1 Immobilization of proteins for single-molecule fluorescence resonance energy transfer measurements of conformation and dynamics.
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    Chapter 2 Application of Confocal Single-Molecule FRET to Intrinsically Disordered Proteins
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    Chapter 3 Single-Molecule Force Spectroscopy of Chimeric Polyprotein Constructs Containing Intrinsically Disordered Domains
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    Chapter 4 Visualization of Mobility by Atomic Force Microscopy
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    Chapter 5 Unequivocal single-molecule force spectroscopy of intrinsically disordered proteins.
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    Chapter 6 Sedimentation Velocity Analytical Ultracentrifugation for Intrinsically Disordered Proteins
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    Chapter 7 Analysis of Intrinsically Disordered Proteins by Small-Angle X-ray Scattering
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    Chapter 8 Small Angle Neutron Scattering for the Structural Study of Intrinsically Disordered Proteins in Solution: A Practical Guide
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    Chapter 9 Dynamic and Static Light Scattering of Intrinsically Disordered Proteins
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    Chapter 10 Estimation of Intrinsically Disordered Protein Shape and Time-Averaged Apparent Hydration in Native Conditions by a Combination of Hydrodynamic Methods
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    Chapter 11 Size-Exclusion Chromatography in Structural Analysis of Intrinsically Disordered Proteins
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    Chapter 12 Denaturant-Induced Conformational Transitions in Intrinsically Disordered Proteins
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    Chapter 13 Identification of Intrinsically Disordered Proteins by a Special 2D Electrophoresis
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    Chapter 14 pH-Induced Changes in Intrinsically Disordered Proteins
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    Chapter 15 Temperature-Induced Transitions in Disordered Proteins Probed by NMR Spectroscopy
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    Chapter 16 Analyzing Temperature-Induced Transitions in Disordered Proteins by NMR Spectroscopy and Secondary Chemical Shift Analyses
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    Chapter 17 Osmolyte-, Binding-, and Temperature-Induced Transitions of Intrinsically Disordered Proteins
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    Chapter 18 Laser Temperature-Jump Spectroscopy of Intrinsically Disordered Proteins
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    Chapter 19 Differential Scanning Microcalorimetry of Intrinsically Disordered Proteins
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    Chapter 20 Identifying Disordered Regions in Proteins by Limited Proteolysis
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    Chapter 21 The Effect of Counter Ions on the Conformation of Intrinsically Disordered Proteins Studied by Size-Exclusion Chromatography
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    Chapter 22 Mean Net Charge of Intrinsically Disordered Proteins: Experimental Determination of Protein Valence by Electrophoretic Mobility Measurements
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    Chapter 23 Protein Characterization by Partitioning in Aqueous Two-Phase Systems
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    Chapter 24 Detection and Characterization of Large-Scale Protein Conformational Transitions in Solution Using Charge-State Distribution Analysis in ESI-MS
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    Chapter 25 Localizing Flexible Regions in Proteins Using Hydrogen–Deuterium Exchange Mass Spectrometry
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    Chapter 26 Mass Spectrometry Tools for Analysis of Intermolecular Interactions
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    Chapter 27 Intrinsically Disordered Protein Analysis
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    Chapter 28 Identifying solubility-promoting buffers for intrinsically disordered proteins prior to purification.
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    Chapter 29 Proteomic Methods for the Identification of Intrinsically Disordered Proteins
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    Chapter 30 Selective Isotope Labeling of Recombinant Proteins in Escherichia coli
Attention for Chapter 28: Identifying solubility-promoting buffers for intrinsically disordered proteins prior to purification.
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Chapter title
Identifying solubility-promoting buffers for intrinsically disordered proteins prior to purification.
Chapter number 28
Book title
Intrinsically Disordered Protein Analysis
Published in
Methods in molecular biology, July 2012
DOI 10.1007/978-1-4614-3704-8_28
Pubmed ID
Book ISBNs
978-1-4614-3703-1, 978-1-4614-3704-8
Authors

Churion KA, Bondos SE, Kelly A. Churion, Sarah E. Bondos, Churion, Kelly A., Bondos, Sarah E.

Abstract

Intrinsically disordered proteins are anticipated to be more prone to aggregation than folded, stable proteins. Chemical additives included in the buffer can help maintain proteins in a soluble, monomeric state. However, the array of chemicals that impact protein solubility is staggering, precluding iterative testing of chemical conditions during purification. Herein, we describe a filter-based aggregation assay to rapidly identify chemical additives that maintain solubility for a protein of interest. A hierarchical approach to buffer selection is provided, in which the type of chemical which best improves solubility is first determined, followed by identifying the optimal chemical and its most effective concentration. Finally, combinations of chemical additives can be assessed if necessary. Although this assay can be applied to purified protein, partially purified protein, or aggregated protein, this protocol specifically details the use of this assay for crude cell lysate. This approach allows identification of solubility-promoting buffers prior to the initial protein purification.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 36 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 1 3%
Unknown 35 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 9 25%
Student > Master 7 19%
Student > Bachelor 6 17%
Researcher 3 8%
Student > Doctoral Student 1 3%
Other 1 3%
Unknown 9 25%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 15 42%
Agricultural and Biological Sciences 7 19%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Physics and Astronomy 1 3%
Neuroscience 1 3%
Other 1 3%
Unknown 10 28%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. 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 04 August 2012.
All research outputs
#15,248,503
of 22,673,450 outputs
Outputs from Methods in molecular biology
#5,287
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Outputs of similar age
#104,490
of 164,635 outputs
Outputs of similar age from Methods in molecular biology
#18
of 58 outputs
Altmetric has tracked 22,673,450 research outputs across all sources so far. This one is in the 22nd percentile – i.e., 22% of other outputs scored the same or lower than it.
So far Altmetric has tracked 13,037 research outputs from this source. They receive a mean Attention Score of 3.3. This one is in the 45th percentile – i.e., 45% of its peers scored the same or lower than it.
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We're also able to compare this research output to 58 others from the same source and published within six weeks on either side of this one. This one has gotten more attention than average, scoring higher than 51% of its contemporaries.