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Synthesis of heptapeptides and analysis of sequence by tandem ion trap mass spectrometry

机译:七肽的合成及串联离子阱质谱分析序列

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Two heptapeptides have been prepared by Fmoc methodology using Wang resin as solid support.For attachment of the first amino acid,several coupling systems were evaluated,and DIC/DMAP system could give yields of>99%and low levels of racemization.The selection of scavenger combination to deprotect side chains revealed that H2O/p-cresol was good at scavenging trityl and 1,2- ethanedithiol was highly e?cient for scavenging t-butyl.Through shortening the preactivation time to 5 min,the racemization which occurred during formation of amide bonds coupled by HBTU was minimized.The crude peptides were characterized by RP-HPLC and MS,and sequenced by MS/MS to acquire reliable amino acid sequence information.
机译:以王氏树脂为固体载体,通过Fmoc方法制备了两种七肽。对于第一个氨基酸的附着,评估了几种偶联体系,DIC / DMAP体系的收率高于99%,外消旋化水平低。清除剂组合对侧链的保护表明,H2O /对甲酚清除三苯甲基的能力强,1,2-乙二硫醇清除叔丁基的能力高。通过将预活化时间缩短至5分钟,消旋作用在形成过程中发生通过RP-HPLC和MS对粗肽进行了表征,并通过MS / MS对其进行了测序,从而获得了可靠的氨基酸序列信息。

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