A system-wide analysis of lipid transfer proteins delineates lipid mobility in human cells
Titeca, K.; Chiapparino, A.; Turei, D.; Zukowska, J.; van Ek, L.; Moqadam, M.; Triana, S.; Nielsen, I. O.; Gehin, C.; Maeda, K.; Alexandrov, T.; Saez-Rodriguez, J.; Reuter, N.; Hennrich, M. L.; Gavin, A.-C.
Show abstract
Lipid transfer proteins (LTPs) maintain the specialised lipid compositions of biological membranes, and many are associated with disease. In eukaryotes, they support organellar functions by transporting lipids between compartmentalised metabolic pathways. However, for the majority of the hundreds of human LTPs, the cargoes remain unknown. We combined biochemical, lipidomic and computational methods to characterize LTP-lipid complexes assembled in cellulo and in an in vitro biochemical assay. We identified bound lipids for about half of the LTPs analysed, and confirmed known cargoes, while discovering new ones for most LTP families. The data represents a systematic resource that captures the general principles of non-vesicular lipid transport in humans. The specificity of LTPs for lipids involves not only the recognition of specific head groups, but also of specific acyl chains. This selectivity defines lipid species within a lipid class with different metabolic or functional fates. The generalised ability of LTPs to form complexes with more than one class of lipids delineates new relationships between lipids and regulatory mechanisms that may contribute to the coordination of metabolism between different organelles. This work represents a resource and a framework for further analyses in different cell types, in pathological states or following various cellular perturbations.
Matching journals
The top 2 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Early Endosome Capture Proteomics and its Application to Amyloid Precursor Protein Intramembrane Processing by β and γ-Secretases 98%
- Structural Basis of Lipopolysaccharide Assembly by the Outer Membrane Translocon Holo-Complex 98%
- TMEM65-dependent Ca2+ extrusion safeguards mitochondrial homeostasis 98%
Similar papers in this journal
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.