Access to Any Site Directed Stable Isotope (2H, 13C, 15N, 17O and 18O) in Genetically Encoded Amino Acids

被引:6
作者
Dawadi, Prativa B. S. [1 ]
Lugtenburg, Johan [1 ]
机构
[1] Leiden Univ, Leiden Inst Chem, NL-2300 RA Leiden, Netherlands
来源
MOLECULES | 2013年 / 18卷 / 01期
关键词
amino acids; isotope labelling; 5-C-13]-leucine; 4-C-13]-valine; C-13 or N-15-enriched L-lysine; O-18]-benzylchloromethyl ether; C-13]-benzonitrile; NATIVE CHEMICAL LIGATION; NMR-SPECTROSCOPY; STEREOSELECTIVE-SYNTHESIS; ASYMMETRIC-SYNTHESIS; METHYL-GROUPS; ENANTIOSELECTIVE SYNTHESIS; DEHYDROAMINO ACIDS; LABELED PROTEINS; L-LEUCINE; EFFICIENT;
D O I
10.3390/molecules18010482
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Proteins and peptides play a preeminent role in the processes of living cells. The only way to study structure-function relationships of a protein at the atomic level without any perturbation is by using non-invasive isotope sensitive techniques with site-directed stable isotope incorporation at a predetermined amino acid residue in the protein chain. The method can be extended to study the protein chain tagged with stable isotope enriched amino acid residues at any position or combinations of positions in the system. In order to access these studies synthetic methods to prepare any possible isotopologue and isotopomer of the 22 genetically encoded amino acids have to be available. In this paper the synthetic schemes and the stable isotope enriched building blocks that are available via commercially available stable isotope enriched starting materials are described.
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页码:482 / 519
页数:38
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