Molecular basis of the glycosomal targeting of PEX11 and its mislocalization to mitochondrion in trypanosomes.

Front Cell Dev Biol

Department of Systems Biochemistry, Institute for Biochemistry and Pathobiochemistry, Faculty of Medicine, Ruhr University Bochum, Bochum, Germany.

Published: August 2023

AI Article Synopsis

  • PEX19 binding sites are crucial for the proper targeting and localization of PEX11, a key peroxisomal and glycosomal membrane protein.
  • There are two main PEX19 binding sites in PEX11, with the N-terminal site being highly conserved and necessary for its effective targeting, while the second site promotes glycosomal localization.
  • Mutations or deletions in these binding sites can cause mislocalization of PEX11 to mitochondria, and the N-terminal region of PEX11 harbors a signal that redirects it to mitochondria when glycosomal transport is impaired.

Article Abstract

PEX19 binding sites are essential parts of the targeting signals of peroxisomal membrane proteins (mPTS). In this study, we characterized PEX19 binding sites of PEX11, the most abundant peroxisomal and glycosomal membrane protein from and . PEX11 contains two PEX19 binding sites, one close to the N-terminus (BS1) and a second in proximity to the first transmembrane domain (BS2). The N-terminal BS1 is highly conserved across different organisms and is required for maintenance of the steady-state concentration and efficient targeting to peroxisomes and glycosomes in both baker's yeast and . The second PEX19 binding site in PEX11 is essential for its glycosomal localization. Deletion or mutations of the PEX19 binding sites in PEX11 or PEX11 results in mislocalization of the proteins to mitochondria. Bioinformatic analysis indicates that the N-terminal region of PEX11 contains an amphiphilic helix and several putative TOM20 recognition motifs. We show that the extreme N-terminal region of PEX11 contains a cryptic N-terminal signal that directs PEX11 to the mitochondrion if its glycosomal transport is blocked.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10469627PMC
http://dx.doi.org/10.3389/fcell.2023.1213761DOI Listing

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