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Heat-enhanced peptide synthesis on Teflon-patterned paper

机译:热转印纸上热增强肽的合成

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摘要

In this report, we describe the methodology for 96 parallel organic syntheses of peptides on Teflon-patterned paper assisted by heating with an infra-red lamp. SPOT synthesis is an important technology for production of peptide arrays on a paper-based support for rapid identification of peptide ligands, epitope mapping, and identification of bio-conjugation reactions. The major drawback of the SPOT synthesis methodology published to-date is suboptimal reaction conversion due to mass transport limitations in the unmixed reaction spot. The technology developed in this report overcomes these problems by changing the environment of the reaction from static to dynamic (flow-through), and further accelerating the reaction by selective heating of the reaction support in contact with activated amino acids. Patterning paper with Teflon allows for droplets of organic solvents to be confined in a zone on the paper array and flow through the paper at a well-defined rate and provide a convenient, power-free setup for flow-through solid-phase synthesis and efficient assembly of peptide arrays. We employed an infra-red (IR) lamp to locally heat the cellulosic support during the flow-through delivery of the reagents to each zone of the paper-based array. We demonstrate that IR-heating in solid phase peptide synthesis shortened the reaction time necessary for amide bond formation down to 3 minutes; in some couplings of alpha amino acids, conversion rates increased up to fifteen folds. The IR-heating improved the assembly of difficult sequences, such as homo-oligomers of all 20 natural amino acids.
机译:在本报告中,我们描述了在聚四氟乙烯图案纸上通过红外灯加热辅助96种平行有机合成肽的方法。 SPOT合成是在纸基支持物上生产肽阵列的重要技术,用于快速鉴定肽配体,表位作图和鉴定生物缀合反应。迄今为止公开的SPOT合成方法的主要缺点是由于未混合反应点中的传质限制而导致次优反应转化。本报告中开发的技术通过将反应环境从静态(动态)更改为动态(流通),并通过选择性加热与活化氨基酸接触的反应载体来进一步加速反应,从而克服了这些问题。使用特富龙对纸张进行图案化处理可将有机溶剂的液滴限制在纸张阵列上的区域中,并以确定的速率流过纸张,并为流经固相合成提供了方便,无动力的设置,并且高效肽阵列的组装。我们在将试剂流通传递到纸基阵列的每个区域的过程中,采用了红外线(IR)灯来局部加热纤维素支持物。我们证明了固相肽合成中的红外加热将酰胺键形成所需的反应时间缩短至3分钟。在某些α氨基酸偶联中,转化率提高了十五倍。红外加热改善了困难序列的组装,例如所有20种天然氨基酸的均聚物。

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