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Unconventional Protein Secretion

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Cover of 'Unconventional Protein Secretion'

Table of Contents

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    Book Overview
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    Chapter 1 ER to Golgi-Dependent Protein Secretion: The Conventional Pathway
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    Chapter 2 Unconventional Protein Secretion
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    Chapter 3 Unconventional Protein Secretion
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    Chapter 4 Chemical Secretory Pathway Modulation in Plant Protoplasts
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    Chapter 5 From Cytosol to the Apoplast: The Hygromycin Phosphotransferase (HYGR) Model in Arabidopsis
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    Chapter 6 Unconventional Protein Secretion
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    Chapter 7 Unconventional Protein Secretion
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    Chapter 8 Quantification of a Non-conventional Protein Secretion: The Low-Molecular-Weight FGF-2 Example
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    Chapter 9 Human Primary Keratinocytes as a Tool for the Analysis of Caspase-1-Dependent Unconventional Protein Secretion
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    Chapter 10 A Reporter System to Study Unconventional Secretion of Proteins Avoiding N-Glycosylation in Ustilago maydis
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    Chapter 11 Stress-Inducible Protein 1 (STI1): Extracellular Vesicle Analysis and Quantification
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    Chapter 12 Unconventional Protein Secretion
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    Chapter 13 Unconventional Protein Secretion
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    Chapter 14 Characterization of the Unconventional Secretion of the Ebola Matrix Protein VP40
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    Chapter 15 Role and Characterization of Synuclein-γ Unconventional Protein Secretion in Cancer Cells
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    Chapter 16 Unconventional Protein Secretion
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    Chapter 17 Unconventional Protein Secretion
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    Chapter 18 Isolation of Exosome-Like Vesicles from Plants by Ultracentrifugation on Sucrose/Deuterium Oxide (D2O) Density Cushions
Attention for Chapter 4: Chemical Secretory Pathway Modulation in Plant Protoplasts
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Chapter title
Chemical Secretory Pathway Modulation in Plant Protoplasts
Chapter number 4
Book title
Unconventional Protein Secretion
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-3804-9_4
Pubmed ID
Book ISBNs
978-1-4939-3802-5, 978-1-4939-3804-9
Authors

Francesca De Marchis, Andrea Pompa, Michele Bellucci

Editors

Andrea Pompa, Francesca De Marchis

Abstract

The classical Golgi pathway is not the only mechanism for vacuolar protein transport in plants because alternative transport mechanisms have been described. The existence of these alternative pathways can be demonstrated using several chemicals and here we describe the use of brefeldin A (BFA), endo-β-N-acetylglucosaminidase H (Endo-H), and tunicamycin, on isolated tobacco leaf protoplasts. Two main methods are illustrated in this chapter, protoplast pulse-chase followed by protein immunoprecipitation, and protoplast immunofluorescence.

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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 2 25%
Researcher 2 25%
Unknown 4 50%
Readers by discipline Count As %
Agricultural and Biological Sciences 2 25%
Nursing and Health Professions 1 13%
Biochemistry, Genetics and Molecular Biology 1 13%
Unknown 4 50%