Research Project
Grant-in-Aid for Young Scientists (B)
Atg8, a ubiquitin-like protein important for membrane dynamics during autophagy, is modified with a phospholipid and localizes to the membrane, thereby contributes to the progression of autophagy. Atg4 is a deconjugating enzyme for lapidated Atg8 and contributes to the recycling of Atg8; however, the regulation mechanism of Atg4 activity remained elusive. Here, I studied the components that regulate Atg4 activity in vitro. The data showed that the activity of Atg4 was affected by neither the interaction with other Atg proteins nor Atg1-mediated phosphorylation, but by the regulatory regions within Atg4. These data suggested that Atg4 might possess an ability to regulate its deconjugating activity depending on the intracellular localization.
All 2017 2016 2015 2014 Other
All Journal Article (6 results) (of which Int'l Joint Research: 1 results, Peer Reviewed: 6 results, Open Access: 4 results, Acknowledgement Compliant: 3 results) Presentation (4 results) (of which Int'l Joint Research: 1 results, Invited: 1 results) Remarks (2 results)
Current Opinion in Structural Biology
Volume: 43 Pages: 10-17
10.1016/j.sbi.2016.09.010
Developmental Cell
Volume: 38 Issue: 1 Pages: 86-99
10.1016/j.devcel.2016.06.015
Molecular Cell
Volume: 60 Issue: 6 Pages: 914-929
10.1016/j.molcel.2015.11.019
Cellular and Molecular Life Sciences
Volume: 72 Issue: 16 Pages: 3083-3096
10.1007/s00018-015-1917-z
Nihon Kessho Gakkaishi
Volume: 57 Issue: 3 Pages: 191-197
10.5940/jcrsj.57.191
130005085906
NATURE STRUCTURAL & MOLECUIAR BIOLOGY
Volume: 21(発表確定) Issue: 6 Pages: 513-521
10.1038/nsmb.2822
http://www.bikaken.or.jp/