A fluorogenic complementation tool kit for interrogating lipid droplet-organelle interaction.


Journal

The Journal of cell biology
ISSN: 1540-8140
Titre abrégé: J Cell Biol
Pays: United States
ID NLM: 0375356

Informations de publication

Date de publication:
02 Sep 2024
Historique:
received: 22 11 2023
revised: 24 04 2024
accepted: 31 05 2024
medline: 1 7 2024
pubmed: 1 7 2024
entrez: 1 7 2024
Statut: ppublish

Résumé

Contact sites between lipid droplets and other organelles are essential for cellular lipid and energy homeostasis upon metabolic demands. Detection of these contact sites at the nanometer scale over time in living cells is challenging. We developed a tool kit for detecting contact sites based on fluorogen-activated bimolecular complementation at CONtact sites, FABCON, using a reversible, low-affinity split fluorescent protein, splitFAST. FABCON labels contact sites with minimal perturbation to organelle interaction. Via FABCON, we quantitatively demonstrated that endoplasmic reticulum (ER)- and mitochondria (mito)-lipid droplet contact sites are dynamic foci in distinct metabolic conditions, such as during lipid droplet biogenesis and consumption. An automated analysis pipeline further classified individual contact sites into distinct subgroups based on size, likely reflecting differential regulation and function. Moreover, FABCON is generalizable to visualize a repertoire of organelle contact sites including ER-mito. Altogether, FABCON reveals insights into the dynamic regulation of lipid droplet-organelle contact sites and generates new hypotheses for further mechanistical interrogation during metabolic regulation.

Identifiants

pubmed: 38949658
pii: 276834
doi: 10.1083/jcb.202311126
pii:
doi:

Substances chimiques

Fluorescent Dyes 0
Luminescent Proteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : American Lebanese Syrian Associated Charities
Organisme : NIH HHS
ID : 1DP2GM150192
Pays : United States

Informations de copyright

© 2024 Li et al.

Auteurs

Xiao Li (X)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Rico Gamuyao (R)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Ming-Lun Wu (ML)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Woo Jung Cho (WJ)

Cell and Tissue Imaging Center, St. Jude Children's Research Hospital, Memphis, TN, USA.

Sharon V King (SV)

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN, USA.

R A Petersen (RA)

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Daniel R Stabley (DR)

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Caleb Lindow (C)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Leslie K Climer (LK)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Abbas Shirinifard (A)

Department of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Francesca Ferrara (F)

Vector Production and Development Laboratory, St. Jude Children's Research Hospital, Memphis, TN, USA.

Robert E Throm (RE)

Vector Production and Development Laboratory, St. Jude Children's Research Hospital, Memphis, TN, USA.

Camenzind G Robinson (CG)

Cell and Tissue Imaging Center, St. Jude Children's Research Hospital, Memphis, TN, USA.

Yiwang Zhou (Y)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, USA.

Alexandre F Carisey (AF)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

Alison G Tebo (AG)

Janelia Research Campus, Howard Hughes Medical Institute, Ashburn, VA, USA.

Chi-Lun Chang (CL)

Department of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, USA.

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