eprintid: 17221 rev_number: 22 userid: 1419 dir: disk0/00/01/72/21 datestamp: 2013-02-08 21:06:42 lastmod: 2021-06-12 23:55:35 status_changed: 2013-02-08 21:06:42 type: article metadata_visibility: show item_issues_count: 0 eprint_status: archive creators_name: Lu, M creators_name: Ahmed, Z creators_name: Mikhonin, AV creators_name: Asher, SA creators_email: creators_email: creators_email: creators_email: asher@pitt.edu creators_id: creators_id: creators_id: creators_id: ASHER title: UV resonance raman measurements of poly-L-lysine's conformational energy landscapes: Dependence on perchlorate concentration and temperature ispublished: pub divisions: sch_as_chemistry full_text_status: public abstract: UV resonance Raman spectroscopy has been used to determine the conformational energy landscape of polyL-lysine (PLL) in the presence of NaClO4 as a function of temperature. At 1 °C, in the presence of 0.83 M NaClO4, PLL shows an ∼86% α-helix-like content, which contains ́-helix and π-bulge/helix conformations. The high a-helix-like content of PLL occurs because of charge screening due to strong ion-pair formation between ClO4- and the lysine side chain -NH3+. As the temperature increases from 1 to 60 °C, the ́-helix and π-bulge/helix conformations melt into extended conformations (PPII and 2.51-helix). We calculate the Ψ Ramachandran angle distribution of the PLL peptide bonds from the UV Raman spectra which allows us to calculate the PLL (un)folding energy landscapes along the Ψ reaction coordinate. We observe a basin in the Ψ angle conformational space associated with α-helix and π-bulge/helix conformations and another basin for the extended PPII and 2.5 1-helical conformations. © 2007 American Chemical Society. date: 2007-07-05 date_type: published publication: Journal of Physical Chemistry B volume: 111 number: 26 pagerange: 7675 - 7680 refereed: TRUE issn: 1520-6106 id_number: 10.1021/jp0703758 pmid: 17567063 mesh_headings: Circular Dichroism mesh_headings: Perchloric Acid--chemistry mesh_headings: Polylysine--chemistry mesh_headings: Protein Conformation mesh_headings: Protein Folding mesh_headings: Sodium Compounds--chemistry mesh_headings: Spectrophotometry, Ultraviolet mesh_headings: Spectrum Analysis, Raman mesh_headings: Temperature mesh_headings: Thermodynamics chemical_names: Sodium Compounds chemical_names: Polylysine chemical_names: Perchloric Acid chemical_names: sodium perchlorate citation: Lu, M and Ahmed, Z and Mikhonin, AV and Asher, SA (2007) UV resonance raman measurements of poly-L-lysine's conformational energy landscapes: Dependence on perchlorate concentration and temperature. Journal of Physical Chemistry B, 111 (26). 7675 - 7680. ISSN 1520-6106 document_url: http://d-scholarship-dev.library.pitt.edu/17221/1/licence.txt