Towards designer organelles by subverting the peroxisomal import pathway

被引:14
作者
Cross, Laura L. [1 ,2 ,3 ]
Paudyal, Rupesh [3 ,4 ]
Kamisugi, Yasuko [4 ,5 ]
Berry, Alan [1 ,3 ]
Cuming, Andrew C. [4 ,5 ]
Baker, Alison [1 ,3 ,4 ]
Warriner, Stuart L. [1 ,2 ]
机构
[1] Univ Leeds, Astbury Ctr Struct Mol Biol, Leeds LS2 9JT, W Yorkshire, England
[2] Univ Leeds, Sch Chem, Leeds LS2 9JT, W Yorkshire, England
[3] Univ Leeds, Sch Mol & Cellular Biol, Leeds LS2 9JT, W Yorkshire, England
[4] Univ Leeds, Ctr Plant Sci, Leeds LS2 9JT, W Yorkshire, England
[5] Univ Leeds, Sch Biol, Leeds LS2 9JT, W Yorkshire, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
SUBCELLULAR TARGETING ANALYSES; PROTEIN-STRUCTURE; IN-VIVO; PTS1; PREDICTION; RECEPTOR; BINDING; PEX5P; PHYSCOMITRELLA; RECOGNITION;
D O I
10.1038/s41467-017-00487-7
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The development of 'designer' organelles could be a key strategy to enable foreign pathways to be efficiently controlled within eukaryotic biotechnology. A fundamental component of any such system will be the implementation of a bespoke protein import pathway that can selectively deliver constituent proteins to the new compartment in the presence of existing endogenous trafficking systems. Here we show that the protein-protein interactions that control the peroxisomal protein import pathway can be manipulated to create a pair of interacting partners that still support protein import in moss cells, but are orthogonal to the naturally occurring pathways. In addition to providing a valuable experimental tool to give new insights into peroxisomal protein import, the variant receptor-signal sequence pair forms the basis of a system in which normal peroxisomal function is downregulated and replaced with an alternative pathway, an essential first step in the creation of a designer organelle.
引用
收藏
页数:9
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