Intrinsic lipid binding activity of ATG 16L1 supports efficient membrane anchoring and autophagy-Reference-Cited by-同舟云学术

Intrinsic lipid binding activity of ATG 16L1 supports efficient membrane anchoring and autophagy

Published:2019-04 Issue:9 Volume:38 Page:
ISSN:0261-4189
Container-title:The EMBO Journal
language:en
Short-container-title:EMBO J

Author:

Dudley Leo J¹,Cabodevilla Ainara G¹,Makar Agata N¹^ORCID,Sztacho Martin²,Michelberger Tim¹,Marsh Joseph A³,Houston Douglas R⁴,Martens Sascha²^ORCID,Jiang Xuejun⁵,Gammoh Noor¹^ORCID

Affiliation:

1. Cancer Research UK Edinburgh Centre Institute of Genetics and Molecular Medicine University of Edinburgh Edinburgh UK

2. Department of Biochemistry and Cell Biology Max F. Perutz Laboratories Vienna Biocenter University of Vienna Vienna Austria

3. Human Genetics Unit Institute of Genetics and Molecular Medicine University of Edinburgh Edinburgh UK

4. Institute of Quantitative Biology, Biochemistry and Biotechnology University of Edinburgh Edinburgh UK

5. Cell Biology Department Memorial Sloan Kettering Cancer Centre New York NY USA

Funder

Cancer Research UK

H2020 European Research Council

Publisher

EMBO

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,Molecular Biology,General Neuroscience

Link

https://onlinelibrary.wiley.com/doi/pdf/10.15252/embj.2018100554

Reference45 articles.

1. Identification, biochemical characterization and crystallization of the central region of human ATG16L1

2. Autophagosome formation from membrane compartments enriched in phosphatidylinositol 3-phosphate and dynamically connected to the endoplasmic reticulum

3. WIPI3 and WIPI4 β-propellers are scaffolds for LKB1-AMPK-TSC signalling circuits in the control of autophagy

4. Two-Site Recognition of Phosphatidylinositol 3-Phosphate by PROPPINs in Autophagy

5. The Phosphatidylinositol 3-Kinase Inhibitors Wortmannin and LY294002 Inhibit Autophagy in Isolated Rat Hepatocytes

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