固相多肽合成树脂的特征和进展
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Camarero.JA和Cotton GJ等[14]报道,在一个3-巯基-3戊酮酰胺-PEG-聚-(N, N-二甲基丙烯酰胺)共聚物上载体(HS-PEGA)上,通过最优化的Boc-SPPS,可以从固相载体上直接得到未保护的多肽。这种方法降低了操作中的损失,明显提高了整个的化学偶联效率。他们合成了几个15-47个残基的肽,并且这种方法可以扩展到用来实现顺序的分子内络合,允许进入大得多的聚合肽和蛋白质系统。
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