TY - CHAP
T1 - Immunofluorescence Labeling of Lipid-Binding Proteins CERTs to Monitor Lipid Raft Dynamics
AU - Giovagnoni, Caterina
AU - Crivelli, Simone M
AU - Losen, Mario
AU - Martinez-Martinez, Pilar
PY - 2021
Y1 - 2021
N2 - Fluorescence microscopy is a powerful and widely used tool in molecular biology. Over the years, the discovery and development of lipid-binding fluorescent probes has established new research possibilities to investigate lipid composition and dynamics in the cell. For instance, fluorescence microscopy has allowed the investigation of lipid localization and density in specific cell compartments such as membranes or organelles. Often, the characteristics and the composition of lipid-enriched structures are determined by analyzing the distribution of a fluorescently labeled lipid probe, which intercalates in lipid-enriched platforms, or specifically binds to parts of the lipid molecule. However, in many cases antibodies targeting proteins have higher specificity and are easier to generate. Therefore, we propose to use both antibodies targeting lipid transporters and lipid binding probes to better monitor lipid membrane changes. As an example, we visualize lipid rafts using the fluorescently labeled-B-subunit of the cholera toxin in combination with antibodies targeting ceramide-binding proteins CERTs, central molecules in the metabolism of sphingolipids.
AB - Fluorescence microscopy is a powerful and widely used tool in molecular biology. Over the years, the discovery and development of lipid-binding fluorescent probes has established new research possibilities to investigate lipid composition and dynamics in the cell. For instance, fluorescence microscopy has allowed the investigation of lipid localization and density in specific cell compartments such as membranes or organelles. Often, the characteristics and the composition of lipid-enriched structures are determined by analyzing the distribution of a fluorescently labeled lipid probe, which intercalates in lipid-enriched platforms, or specifically binds to parts of the lipid molecule. However, in many cases antibodies targeting proteins have higher specificity and are easier to generate. Therefore, we propose to use both antibodies targeting lipid transporters and lipid binding probes to better monitor lipid membrane changes. As an example, we visualize lipid rafts using the fluorescently labeled-B-subunit of the cholera toxin in combination with antibodies targeting ceramide-binding proteins CERTs, central molecules in the metabolism of sphingolipids.
KW - Antibodies/metabolism
KW - Carrier Proteins/metabolism
KW - Cell Line
KW - Cell Membrane/metabolism
KW - Cholera Toxin/metabolism
KW - Fluorescent Antibody Technique/methods
KW - Fluorescent Dyes/metabolism
KW - HEK293 Cells
KW - Humans
KW - Membrane Lipids/metabolism
KW - Membrane Microdomains/metabolism
KW - Membrane Proteins/metabolism
KW - Protein Serine-Threonine Kinases/metabolism
KW - Sphingolipids/metabolism
U2 - 10.1007/978-1-0716-0814-2_19
DO - 10.1007/978-1-0716-0814-2_19
M3 - Chapter
C2 - 32770516
SN - 978-1-0716-0813-5
VL - 2187
T3 - Methods in Molecular Biology
SP - 327
EP - 335
BT - Lipid Rafts
PB - Humana
ER -