Yue Xihua, Bao Mengjing, Christiano Romain, Li Siyang, Mei Jia, Zhu Lianhui, Mao Feifei, Yue Qiang, Zhang Panpan, Jing Shuaiyang, Rothman James E, Qian Yi, Lee Intaek
Shanghai Institute for Advanced Immunochemical Studies, ShanghaiTech University, China.
Department of Genetics and Complex Diseases, School of Public Health, Harvard medical school, Boston, MA, USA.
FEBS Lett. 2017 Sep;591(18):2793-2802. doi: 10.1002/1873-3468.12780. Epub 2017 Aug 21.
Golgin45 plays important roles in Golgi stack assembly and is known to bind both the Golgi stacking protein GRASP55 and Rab2 in the medial-Golgi cisternae. In this study, we sought to further characterize the cisternal adhesion complex using a proteomics approach. We report here that Acyl-CoA binding domain containing 3 (ACBD3) is likely to be a novel binding partner of Golgin45. ACBD3 interacts with Golgin45 via its GOLD domain, while its co-expression significantly increases Golgin45 targeting to the Golgi. Furthermore, ACBD3 recruits TBC1D22, a Rab33b GTPase activating protein (GAP), to a large multi-protein complex containing Golgin45 and GRASP55. These results suggest that ACBD3 may provide a scaffolding to organize the Golgi stacking proteins and a Rab33b-GAP at the medial-Golgi.
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