Literature DB >> 1894598

Carbonmonoxy dopamine beta-hydroxylase. Structural characterization by Fourier transform infrared, fluorescence, and x-ray absorption spectroscopy.

T M Pettingill1, R W Strange, N J Blackburn.   

Abstract

The carbon monoxide complex of ascorbate-reduced dopamine beta-hydroxylase has been prepared and characterized by Fourier transform infrared, fluorescence, and x-ray absorption spectroscopies. CO has previously been shown to be a competitive inhibitor with respect to O2, and binds to only one of the two copper atoms/active site (Blackburn, N. J., Pettingill, T. M., Seagraves, K. S., and Shigeta, R. T. (1990) J. Biol. Chem. 265, 15383-15386). Thus, it acts as an excellent probe of the O2-binding site. A single C-O infrared absorption band is observed at 2089 cm-1, shifting by 46 cm-1 to lower energy on substitution with either 13C16O or 12C18O. The 13C isotope shift is reversed to the position expected for 12CO upon vacuum flushing with 12CO gas, indicating that formation of the CO adduct is a fully reversible process. Binding of the substrate tyramine does not eliminate the infrared peak but causes a 3-cm-1 shift to lower energy. On the other hand, binding of a bifunctional inhibitor which cross-links the substrate and O2-binding site does eliminate the CO peak. These data, in conjunction with the competitive nature of CO binding with respect to O2, identify the CO-binding site as the O2-binding site, and place it in close proximity to the substrate-binding site. CO-dopamine beta-hydroxylase exhibits no luminescence in the visible region, suggesting a structure different from carbonmonoxy hemocyanin, and in all probability mononuclear. Analysis of extended x-ray absorption spectroscopy data is most consistent with an average coordination per Cu of 2-3 histidines, 0.5 CO, and 0.5 S atoms as ligands, and absorption edge comparisons indicates pseudo-4 coordination as the most likely geometry at each Cu(I) center. The results can be interpreted by a model involving inequivalent 4-coordination at each Cu(I) center in the CO adduct with CuAHis3S...CuBHis2CO-X as the coordination most consistent with all of the data.

Entities:  

Mesh:

Substances:

Year:  1991        PMID: 1894598

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  15 in total

Review 1.  Protein design: toward functional metalloenzymes.

Authors:  Fangting Yu; Virginia M Cangelosi; Melissa L Zastrow; Matteo Tegoni; Jefferson S Plegaria; Alison G Tebo; Catherine S Mocny; Leela Ruckthong; Hira Qayyum; Vincent L Pecoraro
Journal:  Chem Rev       Date:  2014-03-24       Impact factor: 60.622

2.  Stopped-Flow Studies of the Reduction of the Copper Centers Suggest a Bifurcated Electron Transfer Pathway in Peptidylglycine Monooxygenase.

Authors:  Shefali Chauhan; Parisa Hosseinzadeh; Yi Lu; Ninian J Blackburn
Journal:  Biochemistry       Date:  2016-03-23       Impact factor: 3.162

3.  The copper centers of tyramine β-monooxygenase and its catalytic-site methionine variants: an X-ray absorption study.

Authors:  Corinna R Hess; Judith P Klinman; Ninian J Blackburn
Journal:  J Biol Inorg Chem       Date:  2010-06-11       Impact factor: 3.358

4.  A copper-methionine interaction controls the pH-dependent activation of peptidylglycine monooxygenase.

Authors:  Andrew T Bauman; Brenda A Broers; Chelsey D Kline; Ninian J Blackburn
Journal:  Biochemistry       Date:  2011-11-22       Impact factor: 3.162

5.  Structure and coordination of CuB in the Acidianus ambivalens aa3 quinol oxidase heme-copper center.

Authors:  Tiago M Bandeiras; Manuel M Pereira; Miguel Teixeira; Pierre Moenne-Loccoz; Ninian J Blackburn
Journal:  J Biol Inorg Chem       Date:  2005-11-02       Impact factor: 3.358

6.  Substrate-Induced Carbon Monoxide Reactivity Suggests Multiple Enzyme Conformations at the Catalytic Copper M-Center of Peptidylglycine Monooxygenase.

Authors:  Chelsey D Kline; Ninian J Blackburn
Journal:  Biochemistry       Date:  2016-11-22       Impact factor: 3.162

7.  Differential reactivity between two copper sites in peptidylglycine α-hydroxylating monooxygenase.

Authors:  Eduardo E Chufán; Sean T Prigge; Xavier Siebert; Betty A Eipper; Richard E Mains; L Mario Amzel
Journal:  J Am Chem Soc       Date:  2010-11-10       Impact factor: 15.419

8.  Rational Design of a Histidine-Methionine Site Modeling the M-Center of Copper Monooxygenases in a Small Metallochaperone Scaffold.

Authors:  Katherine B Alwan; Evan F Welch; Renee J Arias; Ben F Gambill; Ninian J Blackburn
Journal:  Biochemistry       Date:  2019-06-27       Impact factor: 3.162

9.  HHM motif at the CuH-site of peptidylglycine monooxygenase is a pH-dependent conformational switch.

Authors:  Chelsey D Kline; Mary Mayfield; Ninian J Blackburn
Journal:  Biochemistry       Date:  2013-04-05       Impact factor: 3.162

10.  Computational study of the activated O(H) state in the catalytic mechanism of cytochrome c oxidase.

Authors:  Vivek Sharma; Kenneth D Karlin; Mårten Wikström
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-30       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.