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Spatial and temporal dynamics of ATP synthase from mitochondria toward the cell surface.


ABSTRACT: Ectopic ATP synthase complex (eATP synthase), located on cancer cell surface, has been reported to possess catalytic activity that facilitates the generation of ATP in the extracellular environment to establish a suitable microenvironment and to be a potential target for cancer therapy. However, the mechanism of intracellular ATP synthase complex transport remains unclear. Using a combination of spatial proteomics, interaction proteomics, and transcriptomics analyses, we find ATP synthase complex is first assembled in the mitochondria and subsequently delivered to the cell surface along the microtubule via the interplay of dynamin-related protein 1 (DRP1) and kinesin family member 5B (KIF5B). We further demonstrate that the mitochondrial membrane fuses to the plasma membrane in turn to anchor ATP syntheses on the cell surface using super-resolution imaging and real-time fusion assay in live cells. Our results provide a blueprint of eATP synthase trafficking and contribute to the understanding of the dynamics of tumor progression.

SUBMITTER: Chang YW 

PROVIDER: S-EPMC10113393 | biostudies-literature | 2023 Apr

REPOSITORIES: biostudies-literature

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Spatial and temporal dynamics of ATP synthase from mitochondria toward the cell surface.

Chang Yi-Wen YW   Tony Yang T T   Chen Min-Chun MC   Liaw Y-Geh YG   Yin Chieh-Fan CF   Lin-Yan Xiu-Qi XQ   Huang Ting-Yu TY   Hou Jen-Tzu JT   Hung Yi-Hsuan YH   Hsu Chia-Lang CL   Huang Hsuan-Cheng HC   Juan Hsueh-Fen HF  

Communications biology 20230418 1


Ectopic ATP synthase complex (eATP synthase), located on cancer cell surface, has been reported to possess catalytic activity that facilitates the generation of ATP in the extracellular environment to establish a suitable microenvironment and to be a potential target for cancer therapy. However, the mechanism of intracellular ATP synthase complex transport remains unclear. Using a combination of spatial proteomics, interaction proteomics, and transcriptomics analyses, we find ATP synthase comple  ...[more]

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