Ratio of ellipticities between 192 and 208 nm (R1): An effective electronic circular dichroism parameter for characterization of the helical components of proteins and peptides. Issue 11 (7th August 2017)
- Record Type:
- Journal Article
- Title:
- Ratio of ellipticities between 192 and 208 nm (R1): An effective electronic circular dichroism parameter for characterization of the helical components of proteins and peptides. Issue 11 (7th August 2017)
- Main Title:
- Ratio of ellipticities between 192 and 208 nm (R1): An effective electronic circular dichroism parameter for characterization of the helical components of proteins and peptides
- Authors:
- Banerjee, Raja
Sheet, Tridip - Abstract:
- Abstract: Circular dichroism (CD) spectroscopy represents an important tool for characterization of the peptide and protein secondary structures that mainly arise from the conformational disposition of the peptide backbone in solution. In 1991 Manning and Woody proposed that, in addition to the signal intensity, the ratio between [ θ ] n π * and [ θ ] π π * ǁ (( R2 ) ≅ [θ]222 /[θ]208 ), along with [ θ ] π π * ⊥ and [ θ ] π π * ǁ (( R1 ) ≅ [θ]192 /[θ]208 ), may be utilized towards identifying the peptide/protein conformation (especially 310 ‐ and α‐helices). However, till date the use of the ratiometric ellipticity component for helical structure analysis of peptides and proteins has not been reported. We studied a series of temperature dependent CD spectra of a thermally stable, model helical peptide and its related analogs in water as a function of added 2, 2, 2‐trifluoroethanol (TFE) in order to explore their landscape of helicity. For the first time, we have experimentally shown here that the R1 parameter can characterize better the individual helices, while the other parameter R2 and the signal intensity do not always converge. We emphasize the use of the R1 ratio of ellipticities for helical characterization because of the common origin of these two bands (exciton splitting of the amide π→ π* transition in a helical polypeptide). This approach may become worthwhile and timely with the increasing accessibility of CD synchrotron sources.
- Is Part Of:
- Proteins. Volume 85:Issue 11(2017)
- Journal:
- Proteins
- Issue:
- Volume 85:Issue 11(2017)
- Issue Display:
- Volume 85, Issue 11 (2017)
- Year:
- 2017
- Volume:
- 85
- Issue:
- 11
- Issue Sort Value:
- 2017-0085-0011-0000
- Page Start:
- 1975
- Page End:
- 1982
- Publication Date:
- 2017-08-07
- Subjects:
- Aib -- 2, 2, 2‐trifluoroethanol -- CD spectroscopy -- [θ]nπ*/[θ]ππ*ǁ (R2) -- [θ]ππ*⊥/[θ]ππ*ǁ (R1)
Proteins -- Periodicals
Proteins -- Periodicals
572.6 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/prot.25351 ↗
- Languages:
- English
- ISSNs:
- 0887-3585
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6936.164000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14508.xml