Reversible inhibition of mammalian glutamine synthetase by tyrosine nitration

FEBS Letters ◽  
2006 ◽  
Vol 581 (1) ◽  
pp. 84-90 ◽  
Author(s):  
Boris Görg ◽  
Natalia Qvartskhava ◽  
Peter Voss ◽  
Tilman Grune ◽  
Dieter Häussinger ◽  
...  

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Benedikt Frieg ◽  
Boris Görg ◽  
Holger Gohlke ◽  
Dieter Häussinger

Abstract Glutamine synthetase (GS) in the liver is expressed in a small perivenous, highly specialized hepatocyte population and is essential for the maintenance of low, non-toxic ammonia levels in the organism. However, GS activity can be impaired by tyrosine nitration of the enzyme in response to oxidative/nitrosative stress in a pH-sensitive way. The underlying molecular mechanism as investigated by combined molecular simulations and in vitro experiments indicates that tyrosine nitration can lead to a fully reversible and pH-sensitive regulation of protein function. This approach was also used to understand the functional consequences of several recently described point mutations of human GS with clinical relevance and to suggest an approach to restore impaired GS activity.





2011 ◽  
Vol 157 (3) ◽  
pp. 1505-1517 ◽  
Author(s):  
Paula M. Melo ◽  
Liliana S. Silva ◽  
Isa Ribeiro ◽  
Ana R. Seabra ◽  
Helena G. Carvalho


2020 ◽  
Vol 16 (7) ◽  
pp. 4694-4705
Author(s):  
Benedikt Frieg ◽  
Boris Görg ◽  
Natalia Qvartskhava ◽  
Thomas Jeitner ◽  
Nadine Homeyer ◽  
...  


2015 ◽  
Vol 86 ◽  
pp. S30
Author(s):  
Christiane Ott ◽  
Martin Hugo-Pereira ◽  
Walter Meinl ◽  
Nicolás Campolo ◽  
Silvina Bartesaghi ◽  
...  


Hepatology ◽  
2005 ◽  
Vol 41 (5) ◽  
pp. 1065-1073 ◽  
Author(s):  
Boris Görg ◽  
Matthias Wettstein ◽  
Sabine Metzger ◽  
Freimut Schliess ◽  
Dieter Häussinger


Hepatology ◽  
2005 ◽  
Vol 42 (2) ◽  
pp. 499-499 ◽  
Author(s):  
Boris Görg ◽  
Matthias Wettstein ◽  
Sabine Metzger ◽  
Freimut Schliess ◽  
Dieter Häussinger


Author(s):  
W. Kunath ◽  
E. Zeitler ◽  
M. Kessel

The features of digital recording of a continuous series (movie) of singleelectron TV frames are reported. The technique is used to investigate structural changes in negatively stained glutamine synthetase molecules (GS) during electron irradiation and, as an ultimate goal, to look for the molecules' “undamaged” structure, say, after a 1 e/Å2 dose.The TV frame of fig. la shows an image of 5 glutamine synthetase molecules exposed to 1/150 e/Å2. Every single electron is recorded as a unit signal in a 256 ×256 field. The extremely low exposure of a single TV frame as dictated by the single-electron recording device including the electron microscope requires accumulation of 150 TV frames into one frame (fig. lb) thus achieving a reasonable compromise between the conflicting aspects of exposure time per frame of 3 sec. vs. object drift of less than 1 Å, and exposure per frame of 1 e/Å2 vs. rate of structural damage.



2001 ◽  
Vol 13 (1) ◽  
pp. 63-73 ◽  
Author(s):  
J. Balthazart ◽  
M. Baillien ◽  
G. F. Ball


Sign in / Sign up

Export Citation Format

Share Document