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Biophysics of Infection

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Cover of 'Biophysics of Infection'

Table of Contents

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    Book Overview
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    Chapter 1 Biophysics of Infection
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    Chapter 2 Biophysics of Infection
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    Chapter 3 Biophysics of Infection
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    Chapter 4 Biophysics of Infection
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    Chapter 5 Evolution of Drug Resistance in Bacteria
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    Chapter 6 Using Biophysics to Monitor the Essential Protonmotive Force in Bacteria.
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    Chapter 7 Biophysics of Infection
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    Chapter 8 Biophysics of Infection
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    Chapter 9 Biophysics of Infection
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    Chapter 10 Bacterial Surfaces: Front Lines in Host-Pathogen Interaction.
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    Chapter 11 Biophysical Approaches to Bacterial Gene Regulation by Riboswitches
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    Chapter 12 Biophysics of Infection
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    Chapter 13 Transcription Regulation and Membrane Stress Management in Enterobacterial Pathogens.
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    Chapter 14 Biophysics of Infection
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    Chapter 15 Biophysics of Infection
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    Chapter 16 Neutron Reflectivity as a Tool for Physics-Based Studies of Model Bacterial Membranes
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    Chapter 17 Mechanisms of Salmonella Typhi Host Restriction.
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    Chapter 18 Biophysics of Infection
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    Chapter 19 Force Spectroscopy in Studying Infection.
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    Chapter 20 Biophysics of Infection
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    Chapter 21 Biophysics of Infection
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    Chapter 22 Erratum to: The Type I Restriction Enzymes as Barriers to Horizontal Gene Transfer: Determination of the DNA Target Sequences Recognised by Livestock-Associated Methicillin-Resistant Staphylococcus aureus Clonal Complexes 133/ST771 and 398
Attention for Chapter 19: Force Spectroscopy in Studying Infection.
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Chapter title
Force Spectroscopy in Studying Infection.
Chapter number 19
Book title
Biophysics of Infection
Published in
Advances in experimental medicine and biology, May 2016
DOI 10.1007/978-3-319-32189-9_19
Pubmed ID
Book ISBNs
978-3-31-932187-5, 978-3-31-932189-9
Authors

Zhaokun Zhou, Mark C. Leake

Editors

Mark C. Leake

Abstract

Biophysical force spectroscopy tools-for example, optical tweezers, magnetic tweezers, atomic force microscopy-have been used to study elastic, mechanical, conformational and dynamic properties of single biological specimens from single proteins to whole cells to reveal information not accessible by ensemble average methods such as X-ray crystallography, mass spectroscopy, gel electrophoresis and so on. Here, we review the application of these tools on a range of infection-related questions from antibody-inhibited protein processivity to virus-cell adhesion. In each case, we focus on how the instrumental design tailored to the biological system in question translates into the functionality suitable for that particular study. The unique insights that force spectroscopy has gained to complement knowledge learned through population averaging techniques in interrogating biomolecular details prove to be instrumental in therapeutic innovations such as those in structure-based drug design.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 8 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 8 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 38%
Student > Bachelor 2 25%
Lecturer 2 25%
Student > Postgraduate 1 13%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 3 38%
Chemical Engineering 1 13%
Agricultural and Biological Sciences 1 13%
Economics, Econometrics and Finance 1 13%
Chemistry 1 13%
Other 0 0%
Unknown 1 13%