Model peptide for anti-sigma factor domain HHCC zinc fingers: high reactivity toward 1O2 leads to domain unfolding. Issue 12 (21st February 2019)
- Record Type:
- Journal Article
- Title:
- Model peptide for anti-sigma factor domain HHCC zinc fingers: high reactivity toward 1O2 leads to domain unfolding. Issue 12 (21st February 2019)
- Main Title:
- Model peptide for anti-sigma factor domain HHCC zinc fingers: high reactivity toward 1O2 leads to domain unfolding
- Authors:
- Chabert, Valentin
Lebrun, Vincent
Lebrun, Colette
Latour, Jean-Marc
Sénèque, Olivier - Abstract:
- Abstract : The Zn(Cys)2 (His)2 site of the anti-sigma factor ChrR reacts rapidly with 1 O2 supporting its involvement in 1 O2 sensing by this protein. Abstract : All organisms have to cope with the deleterious effects of reactive oxygen species. Some of them are able to mount a transcriptional response to various oxidative stresses, which involves sensor proteins capable of assessing the redox status of the cell or to detect reactive oxygen species. In this article, we describe the design, synthesis and characterization of Zn·LASD (HHCC), a model for the Zn(Cys)2 (His)2 zinc finger site of ChrR, a sensor protein involved in the bacterial defence against singlet oxygen that belongs to the family of zinc-binding anti-sigma factors possessing a characteristic H/C–X24/25 –H–X3 –C–X2 –C motif. The 46-amino acid model peptide LASD (HHCC) was synthetized by solid phase peptide synthesis and its Zn 2+ -binding properties were investigated using electronic absorption, circular dichroism and NMR. LASD (HHCC) forms a 1 : 1 complex with Zn 2+, namely Zn·LASD (HHCC), that adopts a well-defined conformation with the Zn 2+ ion capping a 3-helix core that reproduces almost perfectly the fold of the ChrR in the vicinity of its zinc site. H2 O2 reacts with Zn·LASD (HHCC) to yield a disulfide with a second order rate constant of 0.030 ± 0.002 M −1 s −1 . Zn·LASD (HHCC) reacts rapidly with singlet oxygen to yield sulfinates and sulfonates. A lower limit of the chemical reaction rate constantAbstract : The Zn(Cys)2 (His)2 site of the anti-sigma factor ChrR reacts rapidly with 1 O2 supporting its involvement in 1 O2 sensing by this protein. Abstract : All organisms have to cope with the deleterious effects of reactive oxygen species. Some of them are able to mount a transcriptional response to various oxidative stresses, which involves sensor proteins capable of assessing the redox status of the cell or to detect reactive oxygen species. In this article, we describe the design, synthesis and characterization of Zn·LASD (HHCC), a model for the Zn(Cys)2 (His)2 zinc finger site of ChrR, a sensor protein involved in the bacterial defence against singlet oxygen that belongs to the family of zinc-binding anti-sigma factors possessing a characteristic H/C–X24/25 –H–X3 –C–X2 –C motif. The 46-amino acid model peptide LASD (HHCC) was synthetized by solid phase peptide synthesis and its Zn 2+ -binding properties were investigated using electronic absorption, circular dichroism and NMR. LASD (HHCC) forms a 1 : 1 complex with Zn 2+, namely Zn·LASD (HHCC), that adopts a well-defined conformation with the Zn 2+ ion capping a 3-helix core that reproduces almost perfectly the fold of the ChrR in the vicinity of its zinc site. H2 O2 reacts with Zn·LASD (HHCC) to yield a disulfide with a second order rate constant of 0.030 ± 0.002 M −1 s −1 . Zn·LASD (HHCC) reacts rapidly with singlet oxygen to yield sulfinates and sulfonates. A lower limit of the chemical reaction rate constant between Zn·LASD (HHCC) and 1 O2 was determined to be 3.9 × 10 6 M −1 s −1 . Therefore, the Zn(Cys)2 (His)2 site of Zn·LASD (HHCC) appears to be at least 5 times more reactive toward these two oxidants than that of a classical ββα zinc finger. Consequences for the activation mechanism of ChrR are discussed. … (more)
- Is Part Of:
- Chemical science. Volume 10:Issue 12(2019)
- Journal:
- Chemical science
- Issue:
- Volume 10:Issue 12(2019)
- Issue Display:
- Volume 10, Issue 12 (2019)
- Year:
- 2019
- Volume:
- 10
- Issue:
- 12
- Issue Sort Value:
- 2019-0010-0012-0000
- Page Start:
- 3608
- Page End:
- 3615
- Publication Date:
- 2019-02-21
- Subjects:
- Chemistry -- Periodicals
540.5 - Journal URLs:
- http://pubs.rsc.org/en/Journals/JournalIssues/SC ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c9sc00341j ↗
- Languages:
- English
- ISSNs:
- 2041-6520
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3151.490000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9678.xml