Synthesis of a novel histidine analogue and its efficient incorporation into a protein in vivo.

Yutaka Ikeda, Shun-ichi Kawahara, Masumi Taki, Atsushi Kuno, Tsunemi Hasegawa, Kazunari Taira
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引用次数: 37

Abstract

Proteins containing unnatural amino acids have immense potential in biotechnology and medicine. We prepared several histidine analogues including a novel histidine analogue, beta-(1,2,3-triazol-4-yl)-DL-alanine. These histidine analogues were assayed for translational activity in histidine-auxotrophic Escherichia coli strain UTH780. We observed that several histidine analogues, including our novel histidine analogue, were efficiently incorporated into the protein in vivo; however, other analogues were rejected. These results suggest that the hydrogen atom at a specific position seriously affects incorporation.

一种新的组氨酸类似物的合成及其在体内有效地结合到蛋白质中。
含有非天然氨基酸的蛋白质在生物技术和医学方面具有巨大的潜力。我们制备了几种组氨酸类似物,包括一种新的组氨酸类似物,β -(1,2,3-三唑-4-基)- dl -丙氨酸。测定了这些组氨酸类似物在组氨酸-营养不良大肠杆菌菌株UTH780中的翻译活性。我们观察到几种组氨酸类似物,包括我们的新型组氨酸类似物,在体内有效地结合到蛋白质中;然而,其他类似物被拒绝。这些结果表明,特定位置的氢原子严重影响掺入。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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