Induced Circular Dichroism of Benzyl Chromophores Bound to Helical Polypeptides
Hiroyuki Nomori, Nobuaki Tsuchihashi, Shoji Takagi, Masahiro Hatano
Abstract
Hiroyuki Nomori, Nobuaki Tsuchihashi, Shoji Takagi, Masahiro Hatano
Abstract
Abstract Extrinsic optical activity was observed for symmetric side chain chromophores in helical polypeptides. Poly-β-benzyl-l-aspartate, poly-β-p-nitrobenzyl-l-aspartate and poly-γ-p-nitrobenzyl-l-glutamate gave induced circular dichroism in the wavelength regions corresponding to the absorption bands of the benzyl and the p-nitrobenzyl chromophores of the side chains in their dilute solutions. Moreover, poly-γ-benzyl-d-glutamate gave induced circular dichroism due to the benzyl chromophore in its concentrated solutions which formed a liquid crystalline phase. The extrinsic optical activity thus observed was explained as the consequence of the loss of the rotational freedom of the chromophores relative to the α-helical structure and to the cholesteric helical structure of the polypeptides.
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Abstract Extrinsic optical activity was observed for symmetric side chain chromophores in helical polypeptides. Poly-β-benzyl-l-aspartate, poly-β-p-nitrobenzyl-l-aspartate and poly-γ-p-nitrobenzyl-l-glutamate gave induced circular dichroism in the wavelength regions corresponding to the absorption bands of the benzyl and the p-nitrobenzyl chromophores of the side chains in their dilute solutions. Moreover, poly-γ-benzyl-d-glutamate gave induced circular dichroism due to the benzyl chromophore in its concentrated solutions which formed a liquid crystalline phase. The extrinsic optical activity thus observed was explained as the consequence of the loss of the rotational freedom of the chromophores relative to the α-helical structure and to the cholesteric helical structure of the polypeptides.
Key concepts: Chromophore, Circular dichroism, Chemistry, Side chain, Crystallography, Absorption (acoustics), Stereochemistry, Photochemistry