Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/25357
Author(s): carvalho, af
costa-rodrigues, j
correia, i
pessoa, jc
faria, tq
martins, cl
fransen, m
sa-miranda, c
azevedo, je
Title: The N-terminal half of the peroxisomal cycling receptor Pex5p is a natively unfolded domain
Issue Date: 2006
Abstract: Targeting of most newly synthesised peroxisomal matrix proteins to the organelle requires Pex5p, the so-called PTS1 receptor. According to current models of peroxisomal biogenesis, Pex5p interacts with these proteins in the cytosol, transports them to the peroxisomal membrane and catalyses their translocation across the membrane. Presently, our knowledge on the structural details behind the interaction of Pex5p with the cargo proteins is reasonably complete. In contrast, information regarding the structure of the Pex5p N-terminal half (a region containing its peroxisomal targeting domain) is still limited. We have recently observed that the Stokes radius of this Pex5p domain is anomalously large, suggesting that this portion of the protein is either a structured elongated domain or that it adopts a low compactness conformation. Here, we address this issue using a combination of biophysical and biochemical approaches. Our results indicate that the N-terminal half of Pex5p is best described as a natively unfolded premolten globule-like domain. The implications of these findings on the mechanism of protein import into the peroxisome are discussed.
URI: https://repositorio-aberto.up.pt/handle/10216/25357
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by-nc/4.0/
Appears in Collections:FMDUP - Artigo em Revista Científica Internacional
ICBAS - Artigo em Revista Científica Internacional

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