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Resonance Raman Spectroscopy of the Oxygenated Intermediates of Human CYP19A1 Implicates a Compound I Intermediate in the Final Lyase Step.

Authors :
Mak, Piotr J.
Luthra, Abhinav
Sligar, Stephen G.
Kincaid, James R.
Source :
Journal of the American Chemical Society. 4/2/2014, Vol. 136 Issue 13, p4825-4828. 4p.
Publication Year :
2014

Abstract

CYP19A1, or aromatase, a cytochrome P450 responsible for estrogen biosynthesis in humans, is an important therapeutic target for the treatment of breast cancer. There is still controversy surrounding the identity of reaction intermediate that catalyzes carbon–carbon scission in this key enzyme. Probing the oxy-complexes of CYP19A1 poised for hydroxylase and lyase chemistries using resonance Raman spectroscopy and drawing a comparison with CYP17A1, we have found no significant difference in the frequencies or isotopic shifts for these two steps in CYP19A1. Our experiments implicate the involvement of Compound I in the terminal lyase step of CYP19A1 catalysis. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00027863
Volume :
136
Issue :
13
Database :
Academic Search Index
Journal :
Journal of the American Chemical Society
Publication Type :
Academic Journal
Accession number :
95619184
Full Text :
https://doi.org/10.1021/ja500054c