Human Tim8a, Tim8b and Tim13 are auxiliary assembly factors of mature Complex IV

Author:

Anderson Alexander J12ORCID,Crameri Jordan J12ORCID,Ang Ching‐Seng2,Malcolm Tess R23,Kang Yilin12,Baker Megan J12ORCID,Palmer Catherine S12,Sharpe Alice J4ORCID,Formosa Luke E4,Ganio Katherine5,Baker Michael J12,McDevitt Christopher A5ORCID,Ryan Michael T4ORCID,Maher Megan J236ORCID,Stojanovski Diana12ORCID

Affiliation:

1. Department of Biochemistry and Pharmacology The University of Melbourne Parkville Vic Australia

2. The Bio21 Molecular Science and Biotechnology Institute The University of Melbourne Parkville Vic Australia

3. School of Chemistry The University of Melbourne Parkville Vic Australia

4. Department of Biochemistry and Molecular Biology, Monash Biomedicine Discovery Institute Monash University Clayton Vic Australia

5. Department of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity The University of Melbourne Parkville Vic Australia

6. Department of Biochemistry and Genetics, La Trobe Institute for Molecular Science La Trobe University Bundoora Vic Australia

Abstract

AbstractHuman Tim8a and Tim8b are paralogous intermembrane space proteins of the small TIM chaperone family. Yeast small TIMs function in the trafficking of proteins to the outer and inner mitochondrial membranes. This putative import function for hTim8a and hTim8b has been challenged in human models, but their precise molecular function(s) remains undefined. Likewise, the necessity for human cells to encode two Tim8 proteins and whether any potential redundancy exists is unclear. We demonstrate that hTim8a and hTim8b function in the assembly of cytochrome c oxidase (Complex IV). Using affinity enrichment mass spectrometry, we define the interaction network of hTim8a, hTim8b and hTim13, identifying subunits and assembly factors of the Complex IV COX2 module. hTim8‐deficient cells have a COX2 and COX3 module defect and exhibit an accumulation of the Complex IV S2 subcomplex. These data suggest that hTim8a and hTim8b function in assembly of Complex IV via interactions with intermediate‐assembly subcomplexes. We propose that hTim8–hTim13 complexes are auxiliary assembly factors involved in the formation of the Complex IV S3 subcomplex during assembly of mature Complex IV.

Funder

Australian Research Council

Publisher

Springer Science and Business Media LLC

Subject

Genetics,Molecular Biology,Biochemistry

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3