Exploration of the forbidden regions of the Ramachandran plot (ϕ-ψ) with QTAIM. Issue 38 (25th September 2017)
- Record Type:
- Journal Article
- Title:
- Exploration of the forbidden regions of the Ramachandran plot (ϕ-ψ) with QTAIM. Issue 38 (25th September 2017)
- Main Title:
- Exploration of the forbidden regions of the Ramachandran plot (ϕ-ψ) with QTAIM
- Authors:
- Momen, Roya
Azizi, Alireza
Wang, Lingling
Ping, Yang
Xu, Tianlv
Kirk, Steven R.
Li, Wenxuan
Manzhos, Sergei
Jenkins, Samantha - Abstract:
- Abstract : Left: Response β is defined as: β = arccos(e̲ 2 ·y̲ ) with β * = arccos(e̲ 1 ·y̲ ). Right: QTAIM interpreted Ramachandran plots {( β ϕ, β ϕ *)-( β ψ, β ψ *)} '-' is a hyphen and not a subtraction sign. Pale green and dark green crosses indicate the glycine, pink and red pluses represent the remaining amino acids (a.a.) in the magainin peptide structure. Abstract : A new QTAIM interpretation of the Ramachandran plot is formulated from the most and least facile eigenvectors of the second-derivative matrix of the electron density with a set of 29 magainin-2 peptide conformers. The presence of QTAIM eigenvectors associated with the most and least preferred directions of electronic charge density explained the role of hydrogen bonding, H⋯H contacts and the glycine amino acid monomer in peptide folding. The highest degree of occupation of the QTAIM interpreted Ramachandran plot was found for the glycine amino acid monomer compared with the remaining backbone peptide bonds. The mobility of the QTAIM eigenvectors of the glycine amino acid monomer was higher than for the other amino acids and was comparable to that of the hydrogen bonding, explaining the flexibility of the magainin-2 backbone. We experimented with a variety of hybrid QTAIM–Ramachandran plots to highlight and explain why the glycine amino acid monomer largely occupies the 'forbidden' region on the Ramachandran plot. In addition, the new hybrid QTAIM–Ramachandran plots contained recognizable regions that canAbstract : Left: Response β is defined as: β = arccos(e̲ 2 ·y̲ ) with β * = arccos(e̲ 1 ·y̲ ). Right: QTAIM interpreted Ramachandran plots {( β ϕ, β ϕ *)-( β ψ, β ψ *)} '-' is a hyphen and not a subtraction sign. Pale green and dark green crosses indicate the glycine, pink and red pluses represent the remaining amino acids (a.a.) in the magainin peptide structure. Abstract : A new QTAIM interpretation of the Ramachandran plot is formulated from the most and least facile eigenvectors of the second-derivative matrix of the electron density with a set of 29 magainin-2 peptide conformers. The presence of QTAIM eigenvectors associated with the most and least preferred directions of electronic charge density explained the role of hydrogen bonding, H⋯H contacts and the glycine amino acid monomer in peptide folding. The highest degree of occupation of the QTAIM interpreted Ramachandran plot was found for the glycine amino acid monomer compared with the remaining backbone peptide bonds. The mobility of the QTAIM eigenvectors of the glycine amino acid monomer was higher than for the other amino acids and was comparable to that of the hydrogen bonding, explaining the flexibility of the magainin-2 backbone. We experimented with a variety of hybrid QTAIM–Ramachandran plots to highlight and explain why the glycine amino acid monomer largely occupies the 'forbidden' region on the Ramachandran plot. In addition, the new hybrid QTAIM–Ramachandran plots contained recognizable regions that can be associated with concepts familiar from the conventional Ramachandran plot whilst retaining the character of the QTAIM most and least preferred regions. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 19:Issue 38(2017)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 19:Issue 38(2017)
- Issue Display:
- Volume 19, Issue 38 (2017)
- Year:
- 2017
- Volume:
- 19
- Issue:
- 38
- Issue Sort Value:
- 2017-0019-0038-0000
- Page Start:
- 26423
- Page End:
- 26434
- Publication Date:
- 2017-09-25
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7cp05124g ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4806.xml