Synthesis and stability of N-ε-phospholysine derivatives

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC
Ryanne K. Ballard, Clifford E. Berkman
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引用次数: 0

Abstract

N-ε-Phosphorylated lysine (pLys) residues have been understudied due to their presumed instability to withstand the conventional acidic conditions used in phosphoprotein and phosphopeptide analysis. While some efforts have been made to develop non-hydrolysable pLys surrogates, less progress has been made on developing methods to prepare authentic pLys residue and its derivatives. This study provides a synthetic route to N-ε-phosphorylated lysine models and assesses their pH-dependent stability by use of 31P NMR and HPLC. While the pLys models expectedly showed instability at lower pH (3.5), they showed unexpected stability in moderately acidic conditions (pH 5.0). In addition, the pLys models were sufficiently stable when analyzed utilizing HPLC gradients with an acid modifier (0.1 % TFA).

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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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