Unknown

Dataset Information

0

Crystallographic Characterization of ATG Proteins and Their Interacting Partners.


ABSTRACT: Autophagosome formation and specific substrate recruitment during autophagy require ligation of the ubiquitin-like protein (UBL) Atg8 to the head group of the lipid phosphatidylethanolamine. Atg8 lipidation is mediated by distinctive UBL cascades involving autophagy-specific E1, E2, and E3 enzymes that differ substantially in sequence from components of other UBL conjugation cascades. Structural studies are important for elucidating the roles of Atg proteins that regulate multiple steps involved in autophagy. This chapter describes methods to prepare and crystallize selected proteins and complexes involved in autophagy UBL conjugation pathways, as a guide for strategies for structural and biochemical characterization of Atg proteins.

SUBMITTER: Qiu Y 

PROVIDER: S-EPMC5429400 | biostudies-literature | 2017

REPOSITORIES: biostudies-literature

altmetric image

Publications

Crystallographic Characterization of ATG Proteins and Their Interacting Partners.

Qiu Y Y   Zheng Y Y   Taherbhoy A M AM   Kaiser S E SE   Schulman B A BA  

Methods in enzymology 20161109


Autophagosome formation and specific substrate recruitment during autophagy require ligation of the ubiquitin-like protein (UBL) Atg8 to the head group of the lipid phosphatidylethanolamine. Atg8 lipidation is mediated by distinctive UBL cascades involving autophagy-specific E1, E2, and E3 enzymes that differ substantially in sequence from components of other UBL conjugation cascades. Structural studies are important for elucidating the roles of Atg proteins that regulate multiple steps involved  ...[more]

Similar Datasets

| S-EPMC2711050 | biostudies-literature
| S-EPMC3321844 | biostudies-literature
| S-EPMC4691145 | biostudies-literature
| S-EPMC4502664 | biostudies-literature
| S-EPMC3519869 | biostudies-literature
| S-EPMC8705437 | biostudies-literature
| S-EPMC4648967 | biostudies-literature
| S-EPMC7864983 | biostudies-literature