Cotranslational Folding of a Pentarepeat β-Helix Protein
Notari, Luigi ; Martínez-Carranza, Markel ; Farías-Rico, José Arcadio ; Stenmark, Pål LU
and von Heijne, Gunnar
(2018)
In Journal of Molecular Biology
430(24).
p.5196-5206
- Abstract
It is becoming increasingly clear that many proteins start to fold cotranslationally before the entire polypeptide chain has been synthesized on the ribosome. One class of proteins that a priori would seem particularly prone to cotranslational folding is repeat proteins, that is, proteins that are built from an array of nearly identical sequence repeats. However, while the folding of repeat proteins has been studied extensively in vitro with purified proteins, only a handful of studies have addressed the issue of cotranslational folding of repeat proteins. Here, we have determined the structure and studied the cotranslational folding of a β-helix pentarepeat protein from the human pathogen Clostridium botulinum-a homolog of the... (More)
It is becoming increasingly clear that many proteins start to fold cotranslationally before the entire polypeptide chain has been synthesized on the ribosome. One class of proteins that a priori would seem particularly prone to cotranslational folding is repeat proteins, that is, proteins that are built from an array of nearly identical sequence repeats. However, while the folding of repeat proteins has been studied extensively in vitro with purified proteins, only a handful of studies have addressed the issue of cotranslational folding of repeat proteins. Here, we have determined the structure and studied the cotranslational folding of a β-helix pentarepeat protein from the human pathogen Clostridium botulinum-a homolog of the fluoroquinolone resistance protein MfpA-using an assay in which the SecM translational arrest peptide serves as a force sensor to detect folding events. We find that cotranslational folding of a segment corresponding to the first four of the eight β-helix coils in the protein produces enough force to release ribosome stalling and that folding starts when this unit is ~35 residues away from the P-site, near the distal end of the ribosome exit tunnel. An additional folding transition is seen when the whole PENT moiety emerges from the exit tunnel. The early cotranslational formation of a folded unit may be important to avoid misfolding events in vivo and may reflect the minimal size of a stable β-helix since it is structurally homologous to the smallest known β-helix protein, a four-coil protein that is stable in solution.
(Less)
- author
- Notari, Luigi
; Martínez-Carranza, Markel
; Farías-Rico, José Arcadio
; Stenmark, Pål
LU
and von Heijne, Gunnar
- publishing date
- 2018-12-07
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Journal of Molecular Biology
- volume
- 430
- issue
- 24
- pages
- 5196 - 5206
- publisher
- Elsevier
- external identifiers
-
- pmid:30539762
- scopus:85056415425
- ISSN
- 1089-8638
- DOI
- 10.1016/j.jmb.2018.10.016
- language
- English
- LU publication?
- no
- additional info
- Copyright © 2018 Elsevier Ltd. All rights reserved.
- id
- d73544d5-b468-4fc7-a723-501fca1ce53e
- date added to LUP
- 2019-04-30 07:43:41
- date last changed
- 2024-04-16 03:23:20
@article{d73544d5-b468-4fc7-a723-501fca1ce53e,
abstract = {{<p>It is becoming increasingly clear that many proteins start to fold cotranslationally before the entire polypeptide chain has been synthesized on the ribosome. One class of proteins that a priori would seem particularly prone to cotranslational folding is repeat proteins, that is, proteins that are built from an array of nearly identical sequence repeats. However, while the folding of repeat proteins has been studied extensively in vitro with purified proteins, only a handful of studies have addressed the issue of cotranslational folding of repeat proteins. Here, we have determined the structure and studied the cotranslational folding of a β-helix pentarepeat protein from the human pathogen Clostridium botulinum-a homolog of the fluoroquinolone resistance protein MfpA-using an assay in which the SecM translational arrest peptide serves as a force sensor to detect folding events. We find that cotranslational folding of a segment corresponding to the first four of the eight β-helix coils in the protein produces enough force to release ribosome stalling and that folding starts when this unit is ~35 residues away from the P-site, near the distal end of the ribosome exit tunnel. An additional folding transition is seen when the whole PENT moiety emerges from the exit tunnel. The early cotranslational formation of a folded unit may be important to avoid misfolding events in vivo and may reflect the minimal size of a stable β-helix since it is structurally homologous to the smallest known β-helix protein, a four-coil protein that is stable in solution.</p>}},
author = {{Notari, Luigi and Martínez-Carranza, Markel and Farías-Rico, José Arcadio and Stenmark, Pål and von Heijne, Gunnar}},
issn = {{1089-8638}},
language = {{eng}},
month = {{12}},
number = {{24}},
pages = {{5196--5206}},
publisher = {{Elsevier}},
series = {{Journal of Molecular Biology}},
title = {{Cotranslational Folding of a Pentarepeat β-Helix Protein}},
url = {{http://dx.doi.org/10.1016/j.jmb.2018.10.016}},
doi = {{10.1016/j.jmb.2018.10.016}},
volume = {{430}},
year = {{2018}},
}