scholarly journals In vivo incorporation of multiple unnatural amino acids through nonsense and frameshift suppression

2006 ◽  
Vol 103 (23) ◽  
pp. 8650-8655 ◽  
Author(s):  
E. A. Rodriguez ◽  
H. A. Lester ◽  
D. A. Dougherty
2021 ◽  
Author(s):  
Babu Sudhamalla ◽  
Anirban Roy ◽  
Soumen Barman ◽  
Jyotirmayee Padhan

The site-specific installation of light-activable crosslinker unnatural amino acids offers a powerful approach to trap transient protein-protein interactions both in vitro and in vivo. Herein, we engineer a bromodomain to...


2018 ◽  
Vol 34 (2) ◽  
pp. 179-182 ◽  
Author(s):  
Bertrand Jordan

Alternative bases that can fit into the DNA double helix have now been used in vivo to direct the synthesis of proteins incorporating unnatural amino acids. This bioengineering feat is significant at both the conceptual and the practical levels


1999 ◽  
Vol 276 (1) ◽  
pp. R128-R135 ◽  
Author(s):  
Christiaan Leeuwenburgh ◽  
Polly A. Hansen ◽  
John O. Holloszy ◽  
Jay W. Heinecke

Oxidative damage of proteins has been implicated in disease and aging. In vitro studies demonstrate that two unnatural amino acids, o,o′-dityrosine and o-tyrosine, are stable markers of protein oxidation. We have investigated the possibility that assaying these compounds in urine could provide a noninvasive way to determine levels of protein oxidation in vivo. Isotope dilution gas chromatography-mass spectrometry was used to quantify levels of o,o′-dityrosine and o-tyrosine in skeletal muscle and urine of aging rats subjected to two interventions: 1) dietary antioxidant supplementation and 2) exercise training. In both sedentary rats and exercise-trained rats, antioxidant therapy reduced levels of protein-bound o,o′-dityrosine in skeletal muscle. In contrast, antioxidant therapy or exercise training minimally affected o-tyrosine levels in this tissue. Levels of the oxidized amino acids in urine samples mirrored those of skeletal muscle proteins. Quantification of the levels of oxidized amino acids in urine may thus serve as a noninvasive measure of oxidative stress in vivo because they change in parallel with levels of protein-bound oxidized amino acids in skeletal muscle.


2015 ◽  
Vol 6 (1) ◽  
pp. 770-776 ◽  
Author(s):  
Ivana Drienovská ◽  
Ana Rioz-Martínez ◽  
Apparao Draksharapu ◽  
Gerard Roelfes

Artificial metalloenzymes for asymmetric catalysis were created by in vivo incorporation of unnatural metal binding amino acids into LmrR.


2004 ◽  
Vol 61 (5) ◽  
pp. 1111-1115 ◽  
Author(s):  
G.W Kabalka ◽  
Z.Z Wu ◽  
M-L Yao ◽  
N Natarajan

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