Intracellular Protein Trafficking

Intracellular protein trafficking is the regulated movement of proteins within a cell, ensuring that each molecule reaches the organelle or membrane where it performs its function. Proteins carry targeting signals that are recognized by transport machinery, directing them through pathways such as vesicle-mediated transport between the endoplasmic reticulum, Golgi apparatus, endosomes, lysosomes, and plasma membrane. These routes coordinate secretion, membrane maintenance, organelle function, and protein degradation. Studying intracellular protein trafficking helps explain how cells organize biochemical activities and how defects in sorting or transport contribute to conditions including neurodegeneration, immune dysfunction, and metabolic disease.

Intracellular Protein Trafficking - Related Videos

Research

JoVE Journal - Biology

Imaging the Intracellular Trafficking of APP with Photoactivatable GFP

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Cited by 6 •

2015

While the transport of cell surface proteins is relatively easily studied, visualizing the trafficking of intracellular proteins is much more difficult. Here, we use constructs incorporating photoactivatable GFP and demonstrate a method to accurately follow the amyloid precursor protein from the Golgi apparatus to down-stream compartments and follow its clearance.

Confocal and Super-Resolution Imaging of Polarized Intracellular Trafficking and Secretion of Basement Membrane Proteins During Drosophila Oogenesis

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Cited by 3 •

2022

The basement membrane is essential for tissue and organ morphogenesis during development. To better understand the mechanisms leading to proper placement of this structure, the protocol presented describes methods to visualize and characterize the intracellular trafficking and secretion of basement membrane proteins in epithelial cells using confocal and super-resolution microscopy.

Research

JoVE Journal - Immunology and Infection
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Visualizing Intracellular SNARE Trafficking by Fluorescence Lifetime Imaging Microscopy

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Cited by 5 •

2017

This protocol describes a new method allowing for the quantitative visualization of complex formation of SNARE proteins, based on Förster resonance energy transfer, and fluorescence lifetime imaging microscopy.

Isolation of Cell-Surface and Intracellular Proteins from an Astrocyte Culture

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2025

This video demonstrates the isolation of cell-surface and intracellular proteins from an astrocyte culture. The astrocyte culture is placed on ice to inhibit endocytosis, and then the cell-surface proteins are labeled with a biotinylation reagent. The cells are lysed to release the biotinylated cell-surface proteins and non-biotinylated intracellular proteins. Finally, streptavidin-coated beads are used to separate the biotinylated cell-surface proteins from the intracellular proteins.

Analysis of SCAP N-glycosylation and Trafficking in Human Cells

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Cited by 17 •

2016

We describe a modified method for membrane fraction isolation from human cells and sample preparation for the detection of SCAP N-glycosylation and total protein by using western blot. We further introduce a GFP-labeling method to monitor SCAP trafficking using confocal microscopy. This protocol can be used in regular biology laboratories.

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