Lanyon-Hogg, T, Hooper, J, Gunn, S et al. (2 more authors) (2014) PEX14 binding to Arabidopsis PEX5 has differential effects on PTS1 and PTS2 cargo occupancy of the receptor. FEBS Letters, 588 (14). 2223 - 2229. ISSN 0014-5793
Abstract
PEX5 acts as a cycling receptor for import of PTS1 proteins into peroxisomes and as a co-receptor for PEX7, the PTS2 receptor, but the mechanism of cargo unloading has remained obscure. Using recombinant protein domains we show PEX5 binding to the PEX14N-terminal domain (PEX14N) has no effect on the affinity of PEX5 for a PTS1 containing peptide. PEX5 can form a complex containing both recombinant PTS1 cargo and endogenous PEX7-thiolase simultaneously but isolation of the complex via the PEX14 construct resulted in an absence of thiolase, suggesting a possible role for PEX14 in the unloading of PTS2 cargos.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | (c) 2014, Lanyon-Hogg, T, Hooper, J, Gunn, S, Warriner, SL and Baker, A. This is an Open Access article distributed in accordance with the Creative Commons Attribution (CC BY 4.0) licence, which permits others to distribute, remix, adapt, build upon this work, and license their derivative works on different terms, provided the original work is properly cited. |
Keywords: | Peroxisome; PEX5; PEX7; PEX14; PTS1; PTS2; Cargo unloading; Arabidopsis thaliana |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) |
Depositing User: | Symplectic Publications |
Date Deposited: | 30 Oct 2014 18:11 |
Last Modified: | 16 Jan 2018 05:23 |
Published Version: | http://dx.doi.org/10.1016/j.febslet.2014.05.038 |
Status: | Published |
Publisher: | Elsevier |
Identification Number: | 10.1016/j.febslet.2014.05.038 |
Related URLs: | |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:80869 |