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The Golgi Complex

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Cover of 'The Golgi Complex'

Table of Contents

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    Book Overview
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    Chapter 1 4D Confocal Imaging of Yeast Organelles
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    Chapter 2 Imaging the Polarized Sorting of Proteins from the Golgi Complex in Live Neurons
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    Chapter 3 Imaging Golgi Outposts in Fixed and Living Neurons
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    Chapter 4 Analysis of Arf1 GTPase-Dependent Membrane Binding and Remodeling Using the Exomer Secretory Vesicle Cargo Adaptor
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    Chapter 5 STEM Tomography Imaging of Hypertrophied Golgi Stacks in Mucilage-Secreting Cells
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    Chapter 6 Reconstitution of COPI Vesicle and Tubule Formation
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    Chapter 7 Reconstitution of Phospholipase A2-Dependent Golgi Membrane Tubules
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    Chapter 8 Proteomic Characterization of Golgi Membranes Enriched from Arabidopsis Suspension Cell Cultures
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    Chapter 9 High-Content Analysis of the Golgi Complex by Correlative Screening Microscopy
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    Chapter 10 Activity Detection of GalNAc Transferases by Protein-Based Fluorescence Sensors In Vivo
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    Chapter 11 In Situ Proximity Ligation Assay (PLA) Analysis of Protein Complexes Formed Between Golgi-Resident, Glycosylation-Related Transporters and Transferases in Adherent Mammalian Cell Cultures
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    Chapter 12 Creating Knockouts of Conserved Oligomeric Golgi Complex Subunits Using CRISPR-Mediated Gene Editing Paired with a Selection Strategy Based on Glycosylation Defects Associated with Impaired COG Complex Function
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    Chapter 13 Reversible Controlled Aggregation of Golgi Resident Enzymes to Assess Their Transport/Dynamics Along the Secretory Pathway
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    Chapter 14 Assays to Study the Fragmentation of the Golgi Complex During the G2–M Transition of the Cell Cycle
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    Chapter 15 The Role of Lysophospholipid Acyltransferases in the Golgi Complex
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    Chapter 16 Methods to Purify and Assay Secretory Pathway Kinases
Attention for Chapter 13: Reversible Controlled Aggregation of Golgi Resident Enzymes to Assess Their Transport/Dynamics Along the Secretory Pathway
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Chapter title
Reversible Controlled Aggregation of Golgi Resident Enzymes to Assess Their Transport/Dynamics Along the Secretory Pathway
Chapter number 13
Book title
The Golgi Complex
Published in
Methods in molecular biology, January 2016
DOI 10.1007/978-1-4939-6463-5_13
Pubmed ID
Book ISBNs
978-1-4939-6461-1, 978-1-4939-6463-5
Authors

Riccardo Rizzo, Alberto Luini

Editors

William J. Brown

Abstract

Golgi resident enzymes (GREs) are type II membrane proteins that are responsible for the processing of lipids and proteins within the Golgi stack, mostly by catalyzing the formation of long chains of different sugars bound to their substrates at specific positions. After synthesis and folding, GREs leave the ER to reach the Golgi complex where they are distributed along the Golgi stack in a fashion that reflects the sequential order of the sugar addition reactions they execute. Remarkably, the position of GREs within the stack is not stable; rather, the GREs appear to move rapidly across Golgi cisternae, perhaps to maintain the correct reaction order during the flux of traffic. It would thus be important to understand their dynamics, but methods to analyze their mobility within the stack are lacking. Here, we describe a tool to induce the reversible and controlled aggregation of GREs that can be used to study the ER-to-Golgi transport and intra Golgi dynamics of these enzymes (Rizzo et al., J Cell Biol 201:1027-1036, 2013; Tewari et al., Mol Biol Cell 26:4427-4437, 2015).

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 3 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 3 100%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 1 33%
Researcher 1 33%
Unknown 1 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 1 33%
Agricultural and Biological Sciences 1 33%
Unknown 1 33%