Solid-Phase Fragment Condensation for Synthesis of Peptides from the Immunodominant Sequence of β1-Adrenoreceptor

被引:1
|
作者
Sidorova, M. V. [1 ]
Palkeeva, M. E. [1 ]
Az'muko, A. A. [1 ]
Ovchinnikov, M. V. [1 ]
Molokoedov, A. S. [1 ]
Sharf, T. V. [1 ]
Efremov, E. E. [1 ]
Golitsyn, S. P. [1 ]
机构
[1] Russian Hlth Minist, Russian Cardiol Res & Prod Complex, Moscow 121552, Russia
关键词
the second extracellular loop of the beta(1)-adrenoreceptor; solid-phase peptide synthesis; convergent peptide synthesis; fragment condensation; racemization of a C-terminal amino acid residue; AUTOANTIBODIES; CARDIOMYOPATHY; ANTIGEN; LOOP;
D O I
10.1134/S1068162017040112
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
The P26 peptide corresponding to the 197-222 sequence of the second extracellular loop of the beta(1)-adrenoreceptor (beta(1)-AR) was synthesized by solid-phase fragment condensation on the Wang polymer. Pentapeptide fragments were prepared on the 2-chlorotrityl resin. The racemization degree of the C-terminal alanine residue of the pentapeptide was experimentally evaluated for the synthetic H-Glu-Ser-Asp-Glu-Ala-Arg-OH hexapeptide beta(1)-DR-(202-207) which was prepared by the 5 + 1 fragment condensation with the use of various condensing agents. A content of the diastereoisomeric peptide in the products of the fragment condensation was determined by HPLC on a reversed phase. The D-alanine-containing hexapeptide was specially synthesized and used for a comparison. The minimum racemization degree of the C-terminal alanine residue was observed if complex F was applied to the synthesis of the hexapeptide.
引用
收藏
页码:351 / 358
页数:8
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