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Exocytosis and Endocytosis

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Cover of 'Exocytosis and Endocytosis'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Pharmacological Inhibitors of Exocytosis and Endocytosis: Novel Bullets for Old Targets
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    Chapter 2 Systematic Analysis of Endocytosis by Cellular Perturbations
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    Chapter 3 Real-Time Detection of SNARE Complex Assembly with FRET Using the Tetracysteine System
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    Chapter 4 Profiling Lysine Ubiquitination by Selective Enrichment of Ubiquitin Remnant-Containing Peptides
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    Chapter 5 Secretion of circular proteins using sortase.
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    Chapter 6 Fractionation of Subcellular Membrane Vesicles of Epithelial and Non-epithelial Cells by OptiPrep™ Density Gradient Ultracentrifugation
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    Chapter 7 Combining Pulsed SILAC Labeling and Click-Chemistry for Quantitative Secretome Analysis.
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    Chapter 8 Probabilistic Density Maps to Study the Spatial Organization of Endocytosis
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    Chapter 9 Use of Kaede and Kikume Green–Red Fusions for Live Cell Imaging of G Protein-Coupled Receptors
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    Chapter 10 HaloTag as a Tool to Investigate Peroxisome Dynamics in Cultured Mammalian Cells
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    Chapter 11 SNAP-Tag to Monitor Trafficking of Membrane Proteins in Polarized Epithelial Cells
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    Chapter 12 FlAsH-PALM: Super-resolution Pointillist Imaging with FlAsH-Tetracysteine Labeling
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    Chapter 13 Analysis of protein dynamics with tandem fluorescent protein timers.
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    Chapter 14 Synchronization of Secretory Cargos Trafficking in Populations of Cells
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    Chapter 15 Use of Transmembrane FRET to Investigate the Internalization of Glycosylated Proteins
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    Chapter 16 A Method to Rapidly Induce Organelle-Specific Molecular Activities and Membrane Tethering
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    Chapter 17 A Novel Pair of Split Venus Fragments to Detect Protein–Protein Interactions by In Vitro and In Vivo Bimolecular Fluorescence Complementation Assays
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    Chapter 18 Real-Time Investigation of Plasma Membrane Deformation and Fusion Pore Expansion Using Polarized Total Internal Reflection Fluorescence Microscopy
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    Chapter 19 Nanocones to Study Initial Steps of Endocytosis
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    Chapter 20 A Novel Permeabilization Protocol to Obtain Intracellular 3D Immunolabeling for Electron Tomography
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    Chapter 21 VIS2FIX: Rapid Chemical Fixation of Vitreous Sections for Immuno-Electron Microscopy
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    Chapter 22 Chemical Genomics: Characterizing Target Pathways for Bioactive Compounds Using the Endomembrane Trafficking Network
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    Chapter 23 Application of RNAi Technology and Fluorescent Protein Markers to Study Membrane Traffic in C. elegans
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    Chapter 24 Visualization of clathrin-mediated endocytosis in live Drosophila egg chambers.
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    Chapter 25 A novel extraction protocol to probe the role of cholesterol in synaptic vesicle recycling.
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    Chapter 26 Microfluidic devices for imaging trafficking events in vivo using genetic model organisms.
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    Chapter 27 The “In Situ” Proximity Ligation Assay to Probe Protein–Protein Interactions in Intact Tissues
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    Chapter 28 Exocytosis and Endocytosis
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    Chapter 29 Measurement of Dynamic F-Actin Changes During Exocytosis
Attention for Chapter 26: Microfluidic devices for imaging trafficking events in vivo using genetic model organisms.
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Chapter title
Microfluidic devices for imaging trafficking events in vivo using genetic model organisms.
Chapter number 26
Book title
Exocytosis and Endocytosis
Published in
Methods in molecular biology, January 2014
DOI 10.1007/978-1-4939-0944-5_26
Pubmed ID
Book ISBNs
978-1-4939-0943-8, 978-1-4939-0944-5
Authors

Sudip Mondal, Sandhya P Koushika, Sandhya P. Koushika

Abstract

Miniature devices are powerful new tools that can be used to address multiple questions in biology especially in investigating an individual cell or organism. The primary step forward has been the ease of soft lithography fabrication which has allowed researchers from different disciplines, with incomplete technical knowledge, to develop and use new devices for their own research problems. In this chapter, we describe a simple fabrication process that will allow investigators to make microfluidic devices for in vivo imaging studies using genetic model organisms such as C. elegans, Drosophila larvae, and zebrafish larvae. This microfluidic technology enables detailed studies on multiple cellular and subcellular phenomena including intracellular vesicle trafficking in living organisms over different developmental stages in an anesthetic free environment.

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The data shown below were collected from the profile of 1 X user 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 6 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 6 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 3 50%
Lecturer 2 33%
Professor 1 17%
Readers by discipline Count As %
Engineering 3 50%
Agricultural and Biological Sciences 1 17%
Chemistry 1 17%
Neuroscience 1 17%
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 30 January 2015.
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#20,941,392
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Outputs from Methods in molecular biology
#10,192
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#268,711
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Outputs of similar age from Methods in molecular biology
#410
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