School of Chemistry, Raymond and Beverly Sackler Faculty of Exact Sciences, Tel Aviv University, Tel Aviv 69978, Israel.
Molecules. 2022 Jul 8;27(14):4389. doi: 10.3390/molecules27144389.
Posttranslational modifications (PTMs) dramatically expand the functional diversity of the proteome. The precise addition and removal of PTMs appears to modulate protein structure and function and control key regulatory processes in living systems. Deciphering how particular PTMs affect protein activity is a current frontier in biology and medicine. The large number of PTMs which can appear in several distinct positions, states, and combinations makes preparing such complex analogs using conventional biological and chemical tools challenging. Strategies to access homogeneous and precisely modified proteins with desired PTMs at selected sites and in feasible quantities are critical to interpreting their molecular code. Here, we summarize recent advances in posttranslational chemical mutagenesis and late-stage functionalization chemistry to transfer novel PTM mimicry into recombinant proteins with emphasis on novel transformations.
翻译后修饰(PTMs)极大地扩展了蛋白质组的功能多样性。PTMs 的精确添加和去除似乎调节蛋白质结构和功能,并控制生命系统中的关键调控过程。破译特定 PTMs 如何影响蛋白质活性是生物学和医学的当前前沿领域。大量的 PTMs 可以出现在几个不同的位置、状态和组合中,这使得使用传统的生物和化学工具来制备这种复杂的类似物具有挑战性。获取具有所需 PTMs 的同质且精确修饰的蛋白质的策略对于解释其分子密码至关重要。在这里,我们总结了最近在翻译后化学诱变和晚期功能化化学方面的进展,以将新型 PTM 模拟物转移到重组蛋白中,重点介绍新型转化。