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Synthesis of sulfur-35 reagents for protein labeling

机译:硫35蛋白质标记试剂的合成

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摘要

Two ~(35)S reagents were developed to radiolabel proteins. The first reagent, a JV-hydroxysuccinimide (NHS) ester (SMSB), acylates the s-amino group of lysine residues in proteins. The second reagent, an aldehyde (MSAPPA), labels lysine residues via reductive alkylation. Comparing the two methods, the reductive alkylation method labeled proteins over a broader pH range with higher overall radiochemical yield. The biological activity of the proteins did not change Nter labeling with these ~(35)S reagents.
机译:开发了两种〜(35)S试剂来放射性标记蛋白质。第一种试剂是JV-羟基琥珀酰亚胺(NHS)酯(SMSB),可将蛋白质中赖氨酸残基的s-氨基酰化。第二种试剂,醛(MSAPPA),通过还原烷基化标记赖氨酸残基。比较这两种方法,还原烷基化方法在较宽的pH范围内标记了蛋白质,并具有较高的总放射化学产率。这些〜(35)S试剂的蛋白质生物学活性没有改变Nter标记。

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