scholarly journals Electron spin relaxation enhancement measurements of interspin distances in human, porcine, and Rhodobacter electron transfer flavoprotein–ubiquinone oxidoreductase (ETF–QO)

2008 ◽  
Vol 190 (2) ◽  
pp. 222-232 ◽  
Author(s):  
Alistair J. Fielding ◽  
Robert J. Usselman ◽  
Nicholas Watmough ◽  
Martin Simkovic ◽  
Frank E. Frerman ◽  
...  
2021 ◽  
Vol 125 (3) ◽  
pp. 841-849 ◽  
Author(s):  
Krzysztof Tadyszak ◽  
Radosław Mrówczyński ◽  
Raanan Carmieli

2016 ◽  
Vol 108 (8) ◽  
pp. 082103 ◽  
Author(s):  
S. Azaizia ◽  
A. Balocchi ◽  
H. Carrère ◽  
P. Renucci ◽  
T. Amand ◽  
...  

1988 ◽  
Vol 255 (3) ◽  
pp. 869-876 ◽  
Author(s):  
D J Steenkamp

The mitochondrial electron-transfer flavoprotein (ETF) is a heterodimer containing only one FAD. In previous work on the structure-function relationships of ETF, its interaction with the general acyl-CoA dehydrogenase (GAD) was studied by chemical cross-linking with heterobifunctional reagents [D. J. Steenkamp (1987) Biochem. J. 243, 519-524]. GAD whose lysine residues were substituted with 3-(2-pyridyldithio)propionyl groups was preferentially cross-linked to the small subunit of ETF, the lysine residues of which had been substituted with 4-mercaptobutyramidine (MBA) groups. This work was extended to the interaction of ETF with ETF-ubiquinone oxidoreductase (ETF-Q ox). ETF-Q ox was partially inactivated by modification with N-succinimidyl 3-(2-pyridyldithio)propionate to introduce pyridyl disulphide structures. A similar modification of ETF caused a large increase in the apparent Michaelis constant of ETF-Q ox for modified ETF owing to the loss of positive charge on some critical lysines of ETF. When ETF-Q ox was modified with 2-iminothiolane to introduce 4-mercaptobutyramidine groups, only a minor effect on the activity of the enzyme was observed. To retain the positive charges on the lysine residues of ETF, pyridyl disulphide structures were introduced by treating ETF with 2-iminothiolane in the presence of 2,2′-dithiodipyridyl. The electron-transfer activity of the resultant ETF preparation containing 4-(2-pyridyldithio)butyramidine (PDBA) groups was only slightly affected. When ETF-Q ox substituted with MBA groups was mixed with ETF bearing PDBA groups, at least 70% of the cross-links formed between the two proteins were between the small subunit of ETF and ETF-Q ox. ETF-Q ox, therefore, interacts predominantly with the same subunit of ETF as GAD. Variables which affect the selectivity of ETF-Q ox cross-linking to the subunits of ETF are considered.


2005 ◽  
Vol 72 (15) ◽  
Author(s):  
Michio Ikezawa ◽  
Bipul Pal ◽  
Yasuaki Masumoto ◽  
Ivan V. Ignatiev ◽  
Sergey Yu. Verbin ◽  
...  

1979 ◽  
Vol 42 (26) ◽  
pp. 1773-1776 ◽  
Author(s):  
S. R. Kurtz ◽  
H. J. Stapleton

2016 ◽  
Vol 33 (10) ◽  
pp. 107802
Author(s):  
Bing-Hui Niu ◽  
Teng-Fei Yan ◽  
Hai-Qiao Ni ◽  
Zhi-Chuan Niu ◽  
Xin-Hui Zhang

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