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Membrane targeting of core autophagy players during autophagosome biogenesis
被引:14
|作者:
Dudley, Leo J.
[1
]
Makar, Agata N.
[1
]
Gammoh, Noor
[1
]
机构:
[1] Univ Edinburgh, Inst Genet & Mol Med, Canc Res UK Edinburgh Ctr, Crewe Rd South, Edinburgh EH4 2XR, Midlothian, Scotland
关键词:
ATG;
autophagosome;
autophagy;
membrane recruitment;
phagophore;
PI(3)P;
ULK1;
COMPLEX;
STRUCTURAL BASIS;
PHOSPHATIDYLINOSITOL;
3-PHOSPHATE;
ENDOPLASMIC-RETICULUM;
ATG12-ATG5;
CONJUGATE;
SELECTIVE AUTOPHAGY;
LC3;
CONJUGATION;
FORMATION SITE;
ATG PROTEINS;
ATG16L1;
D O I:
10.1111/febs.15334
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Autophagosomes are vital organelles required to facilitate the lysosomal degradation of cytoplasmic cargo, thereby playing an important role in maintaining cellular homeostasis. A number of autophagy-related (ATG) protein complexes are recruited to the site of autophagosome biogenesis where they act to facilitate membrane growth and maturation. Regulated recruitment of ATG complexes to autophagosomal membranes is essential for their autophagic activities and is required to ensure the efficient engulfment of cargo destined for lysosomal degradation. In this review, we discuss our current understanding of the spatiotemporal hierarchy between ATG proteins, examining the mechanisms underlying their recruitment to membranes. A particular focus is placed on the relevance of phosphatidylinositol 3-phosphate and the extent to which the core autophagy players are reliant on this lipid for their localisation to autophagic membranes. In addition, open questions and potential future research directions regarding the membrane recruitment and displacement of ATG proteins are discussed here.
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页码:4806 / 4821
页数:16
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