Stereospecific assignment of leucine methyl groups with carbon-13 in natural abundance or with random 13C labeling

1992 ◽  
Vol 114 (3) ◽  
pp. 1126-1127 ◽  
Author(s):  
M. Sattler ◽  
H. Schwalbe ◽  
C. Griesinger
2015 ◽  
Vol 252 ◽  
pp. 10-19 ◽  
Author(s):  
Hannes Klaus Fasshuber ◽  
Jean-Philippe Demers ◽  
Veniamin Chevelkov ◽  
Karin Giller ◽  
Stefan Becker ◽  
...  

2007 ◽  
Vol 129 (44) ◽  
pp. 13749-13757 ◽  
Author(s):  
Michael John ◽  
Christophe Schmitz ◽  
Ah Young Park ◽  
Nicholas E. Dixon ◽  
Thomas Huber ◽  
...  

2020 ◽  
Author(s):  
Polla Rouf ◽  
Pitsiri Sukkaew ◽  
Lars Ojamäe ◽  
Henrik Pedersen

<p>Aluminium nitride (AlN) is a semiconductor with a wide range of applications from light emitting diodes to high frequency transistors. Electronic grade AlN is routinely deposited at 1000 °C by chemical vapour deposition (CVD) using trimethylaluminium (TMA) and NH<sub>3</sub> while low temperature CVD routes to high quality AlN are scarce and suffer from high levels of carbon impurities in the film. We report on an ALD-like CVD approach with time-resolved precursor supply where thermally induced desorption of methyl groups from the AlN surface is enhanced by the addition of an extra pulse, H<sub>2</sub>, N<sub>2</sub> or Ar between the TMA and NH<sub>3</sub> pulses. The enhanced desorption allowed deposition of AlN films with carbon content of 1 at. % at 480 °C. Kinetic- and quantum chemical modelling suggest that the extra pulse between TMA and NH<sub>3</sub> prevents re-adsorption of desorbing methyl groups terminating the AlN surface after the TMA pulse. </p>


2019 ◽  
Author(s):  
Michelle Gill ◽  
Andrew Hsu ◽  
Arthur G. Palmer, III

<div> <div> <div> <p>The zero- and double-quantum methyl TROSY Hahn-echo and the methyl <sup>1</sup>H-<sup>1</sup>H dipole- dipole cross-correlation nuclear magnetic resonance experiments enable estimation of multiple quantum chemical exchange broadening in methyl groups in proteins. The two relaxation rate constants are established to be linearly dependent using molecular dynamics simulations and empirical analysis of experimental data. This relationship allows chemical exchange broadening to be recognized as an increase in the Hahn-echo relaxation rate constant. The approach is illustrated by analyzing relaxation data collected at three temperatures for <i>E. coli </i>ribonuclease HI and by analyzing relaxation data collected for different cofactor and substrate complexes of <i>E. coli </i>AlkB. </p> </div> </div> </div>


1981 ◽  
Vol 45 (2) ◽  
pp. 450-451 ◽  
Author(s):  
Daniel H. Kohl ◽  
Barbara A. Bryan ◽  
Georgia Shearer ◽  
Ross A. Virginia

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