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Protein Amyloid Aggregation

Overview of attention for book
Cover of 'Protein Amyloid Aggregation'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Semisynthesis and Enzymatic Preparation of Post-translationally Modified α-Synuclein.
  3. Altmetric Badge
    Chapter 2 Isotope-Labeled Amyloids via Synthesis, Expression, and Chemical Ligation for Use in FTIR, 2D IR, and NMR Studies.
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    Chapter 3 Intermolecular Paramagnetic Relaxation Enhancement (PRE) Studies of Transient Complexes in Intrinsically Disordered Proteins.
  5. Altmetric Badge
    Chapter 4 Detection of Helical Intermediates During Amyloid Formation by Intrinsically Disordered Polypeptides and Proteins.
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    Chapter 5 Fluorescence Correlation Spectroscopy: A Tool to Study Protein Oligomerization and Aggregation In Vitro and In Vivo.
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    Chapter 6 Deep UV Resonance Raman Spectroscopy for Characterizing Amyloid Aggregation
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    Chapter 7 Analyzing Tau Aggregation with Electron Microscopy.
  9. Altmetric Badge
    Chapter 8 Characterization of Amyloid Oligomers by Electrospray Ionization-Ion Mobility Spectrometry-Mass Spectrometry (ESI-IMS-MS).
  10. Altmetric Badge
    Chapter 9 Formation and Characterization of α-Synuclein Oligomers.
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    Chapter 10 Fluorescence Methods for Unraveling Oligomeric Amyloid Intermediates
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    Chapter 11 Preparation of Amyloid Fibrils for Magic-Angle Spinning Solid-State NMR Spectroscopy
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    Chapter 12 Spin Labeling and Characterization of Tau Fibrils Using Electron Paramagnetic Resonance (EPR).
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    Chapter 13 Preparation of Crystalline Samples of Amyloid Fibrils and Oligomers
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    Chapter 14 Quenched Hydrogen Exchange NMR of Amyloid Fibrils
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    Chapter 15 Studying the Early Stages of Protein Aggregation Using Replica Exchange Molecular Dynamics Simulations
  17. Altmetric Badge
    Chapter 16 Computational Methods for Structural and Functional Studies of Alzheimer's Amyloid Ion Channels.
  18. Altmetric Badge
    Chapter 17 Analyzing Ensembles of Amyloid Proteins Using Bayesian Statistics
  19. Altmetric Badge
    Chapter 18 In Vitro Studies of Membrane Permeability Induced by Amyloidogenic Polypeptides Using Large Unilamellar Vesicles
  20. Altmetric Badge
    Chapter 19 Cell Models to Study Cell-to-Cell Transmission of α-Synuclein.
  21. Altmetric Badge
    Chapter 20 Preparation of Amyloid Fibrils Seeded from Brain and Meninges.
Attention for Chapter 5: Fluorescence Correlation Spectroscopy: A Tool to Study Protein Oligomerization and Aggregation In Vitro and In Vivo.
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About this Attention Score

  • In the top 25% of all research outputs scored by Altmetric
  • High Attention Score compared to outputs of the same age (80th percentile)
  • High Attention Score compared to outputs of the same age and source (87th percentile)

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Chapter title
Fluorescence Correlation Spectroscopy: A Tool to Study Protein Oligomerization and Aggregation In Vitro and In Vivo.
Chapter number 5
Book title
Protein Amyloid Aggregation
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-2978-8_5
Pubmed ID
Book ISBNs
978-1-4939-2977-1, 978-1-4939-2978-8
Authors

Sahoo, Bankanidhi, Drombosky, Kenneth W, Wetzel, Ronald, Bankanidhi Sahoo, Kenneth W. Drombosky, Ronald Wetzel

Abstract

Fluorescence correlation spectroscopy (FCS) is a highly sensitive analytical technique used to measure dynamic molecular parameters, such as diffusion time (from which particle size can be calculated), conformation, and concentration of fluorescent molecules. It has been particularly powerful in characterizing size distributions in molecular associations (e.g., dimer/multimer formation) both in well-behaved thermodynamically equilibrated systems in vitro as well as in more complex environments in vivo. Protein aggregation reactions like amyloid formation, in contrast, are complex, often involving a series of uniquely structured aggregation intermediates appearing at different time scales. Nonetheless, FCS can be used in appropriate cases to characterize the early stages of some aggregation reactions. Here are described step-by-step protocols and experimental procedures for the study of molecular complex formation in aggregation systems as observed in simple buffer systems, cell extracts, and living cells. The methods described are illustrated with examples from studies of the self-assembly of huntingtin fragments, but in principle can be adapted for any aggregating system.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 34 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 34 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 11 32%
Student > Master 5 15%
Researcher 5 15%
Student > Bachelor 2 6%
Other 1 3%
Other 1 3%
Unknown 9 26%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 11 32%
Agricultural and Biological Sciences 4 12%
Chemistry 3 9%
Physics and Astronomy 2 6%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Other 2 6%
Unknown 11 32%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 7. 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 16 October 2015.
All research outputs
#4,180,223
of 22,829,683 outputs
Outputs from Methods in molecular biology
#1,132
of 13,125 outputs
Outputs of similar age
#71,809
of 393,540 outputs
Outputs of similar age from Methods in molecular biology
#168
of 1,470 outputs
Altmetric has tracked 22,829,683 research outputs across all sources so far. Compared to these this one has done well and is in the 80th percentile: it's in the top 25% of all research outputs ever tracked by Altmetric.
So far Altmetric has tracked 13,125 research outputs from this source. They receive a mean Attention Score of 3.4. This one has done particularly well, scoring higher than 90% 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 393,540 tracked outputs that were published within six weeks on either side of this one in any source. This one has done well, scoring higher than 80% of its contemporaries.
We're also able to compare this research output to 1,470 others from the same source and published within six weeks on either side of this one. This one has done well, scoring higher than 87% of its contemporaries.