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Updated: Aug 14, 2026

Fluorescence-Based Measurements of Phosphatidylserine/Phosphatidylinositol 4-Phosphate Exchange Between Membranes
Published on: March 14, 2021
An internal region of the peroxisomal membrane protein PMP47 is essential for sorting to peroxisomes
M T McCammon1, J A McNew, P J Willy
1Department of Pharmacology, University of Texas Southwestern Medical Center, Dallas 75235-9041.
Abstract:
Targeting sequences on peroxisomal membrane proteins have not yet been identified. We have attempted to find such a sequence within PMP47, a protein of the methylotrophic yeast, Candida boidinii. This protein of 423 amino acids shows sequence similarity with proteins in the family of mitochondrial carrier proteins. As such, it is predicted to have six membrane-spanning domains. Protease susceptibility experiments are consistent with a six-membrane-spanning model for PMP47, although the topology for the peroxisomal protein is inverted compared with the mitochondrial carrier proteins. PMP47 contains two potential peroxisomal targeting sequences (PTS1), an internal SKL (residues 320-322) and a carboxy terminal AKE (residues 421-423). Using a heterologous in vivo sorting system, we show that efficient sorting occurs in the absence of both sequences. Analysis of PMP47-dihydrofolate reductase (DHFR) fusion proteins revealed that amino acids 1-199 of PMP47, which contain the first three putative membrane spans, do not contain the necessary targeting information, whereas a fusion with amino acids 1-267, which contains five spans, is fully competent for sorting to peroxisomes. Similarly, a DHFR fusion construct containing residues 268-423 did not target to peroxisomes while residues 203-420 appeared to sort to that organelle, albeit at lower efficiency than the 1-267 construct. However, DHFR constructs containing only amino acids 185-267 or 203-267 of PMP47 were not found to be associated with peroxisomes. We conclude that amino acids 199-267 are necessary for peroxisomal targeting, although additional sequences may be required for efficient sorting to, or retention by, the organelles.
Insights
Researchers identified a specific region within the PMP47 protein of Candida boidinii that is crucial for peroxisomal targeting. This finding advances our understanding of how proteins are sorted to peroxisomes.
Area of Science:
- Cell Biology
- Molecular Biology
- Protein Trafficking
Background:
- Peroxisomal membrane proteins (PMPs) play vital roles in cellular functions.
- Identifying targeting sequences for PMPs is essential for understanding protein localization.
- PMP47 from Candida boidinii is structurally similar to mitochondrial carrier proteins but with inverted topology.
Purpose of the Study:
- To identify targeting sequences within PMP47 for peroxisomal localization.
- To investigate the role of potential peroxisomal targeting signals (PTS1) in PMP47 sorting.
- To determine the specific protein domains responsible for PMP47 targeting to peroxisomes.
Main Methods:
- Protease susceptibility experiments to determine membrane topology.
- Heterologous in vivo sorting assays using PMP47-dihydrofolate reductase (DHFR) fusion proteins.
- Analysis of PMP47 deletion and truncation mutants for peroxisomal association.
Main Results:
- PMP47 exhibits a six-membrane-spanning topology, inverted compared to mitochondrial carriers.
- The canonical peroxisomal targeting sequences (PTS1), SKL and AKE, are not essential for PMP47 sorting.
- Amino acids 199-267 of PMP47 are necessary for peroxisomal targeting, with residues 1-267 showing efficient sorting.
Conclusions:
- Peroxisomal targeting of PMP47 is mediated by a region distinct from known PTS1 sequences.
- The identified region (amino acids 199-267) is critical for peroxisomal targeting, though additional factors may influence efficient sorting and retention.
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