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Disulfide bond dihedral angles from Raman spectroscopy.

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TLDR
The linear dependence of the S-S stretching frequency on dihedral angle leads to a dihedral angles for the plant hormone, malformin A, that is in excellent agreement with that estimated from the longest wavelength CS-SC ultraviolet absorption band.
Abstract
Raman spectra of several compounds containing the CS-SC moiety were obtained (in the solid phase) from 450-800 cm(-1) to investigate the S-S and C-S stretching behavior. The S-S stretching frequency varied linearly with the CS-SC dihedral angle (obtained from either x-ray or neutron diffraction or ultraviolet absorption) for compounds whose CC-SS dihedral angles were not very different. The ratio of the intensities of the S-S and C-S stretching bands exhibited no recognizable correlation with either the CS-SC dihedral angle or the CSS bond angle, probably because this ratio is sensitive to the crystalline environment. The linear dependence of the S-S stretching frequency on dihedral angle leads to a dihedral angle for the plant hormone, malformin A, that is in excellent agreement with that estimated from the longest wavelength CS-SC ultraviolet absorption band.

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Book ChapterDOI

The anatomy and taxonomy of protein structure.

TL;DR: This chapter investigates the anatomy and taxonomy of protein structures, based on the results of three-dimensional X-ray crystallography of globular proteins.
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Vibrational spectroscopy and conformation of peptides, polypeptides, and proteins.

TL;DR: The aim of this chapter is to present recent developments in the vibrational spectroscopy of peptides, polypeptides, and proteins.
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Recent Advances in the Applications of Ionic Liquids in Protein Stability and Activity: A Review

TL;DR: The methods used for studying the protein–IL interaction are analyzed, useful in providing information about structural and conformational dynamics of protein and the affect of physico-chemical properties of ionic liquids, viz. hydrogen bond capacity and hydrophobicity on protein stability are discussed.
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Raman spectroscopy of protein pharmaceuticals.

TL;DR: Various Raman techniques that can be used for protein pharmaceutical studies are reviewed and novel Raman marker of proteins discovered from fundamental studies of protein complexes are examined along with established Raman spectra and structure correlations.
References
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Journal ArticleDOI

Structure of crystalline -chymotrypsin. V. The atomic structure of tosyl- -chymotrypsin at 2 A resolution.

TL;DR: Refined atomic co-ordinates for tosyl-α-chymotrypsin have been obtained by computational refinement of co-coordinates derived from a carefully built atomic model as mentioned in this paper.
Journal ArticleDOI

Laser-excited Raman spectroscopy of biomolecules: I. Native lysozyme and its constituent amino acids☆

TL;DR: Laser-excited Raman spectra of a simple native protein, lysozyme, in aqueous solution are reported and partially interpreted with the help of the specta of its constituent amino acids and appear to be potentially useful in assessment of conformational changes caused by denaturation.
Journal ArticleDOI

Laser-excited Raman spectroscopy of biomolecules: II. Native ribonuclease and α-chymotrypsin☆☆☆

TL;DR: In this paper, the laser-excited Raman spectra of native ribonuclease and α-chymotrypsin and of the polypeptide poly-l-glutamic acid have been determined in aqueous solution.
Journal ArticleDOI

Laser Raman spectroscopy and the conformation of insulin and proinsulin.

TL;DR: Analysis of laser-excited Raman spectra of proinsulin in the solid state and aqueous solution indicates that extensive conformational changes have taken place in the conversion of native to denatured fibrous insulin and that fibrous diabetes exists in a β-conformation as proposed by Ambrose & Elliott (1951).
Journal ArticleDOI

Laser Raman scattering of cobramine B, a basic protein from cobra venom.

TL;DR: Cobramine B, a small basic protein from cobra venom, is selected as a model for studying the scattering intensity of tyrosyl ring vibrations in the Raman spectra of proteins, suggesting that this protein may contain a large fraction of antiparallel-β structure.
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