Designing disorder: Tales of the unexpected tails.

David P Minde, Els F Halff, Sander Tans
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引用次数: 18

Abstract

Protein tags of various sizes and shapes catalyze progress in biosciences. Well-folded tags can serve to solubilize proteins. Small, unfolded, peptide-like tags have become invaluable tools for protein purification as well as protein-protein interaction studies. Intrinsically Disordered Proteins (IDPs), which lack unique 3D structures, received exponentially increasing attention during the last decade. Recently, large ID tags have been developed to solubilize proteins and to engineer the pharmacological properties of protein and peptide pharmaceuticals. Here, we contrast the complementary benefits and applications of both folded and ID tags based on predictions of ID. Less structure often means more function in a shorter tag.

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设计混乱:意想不到的尾巴的故事。
各种大小和形状的蛋白质标签催化了生物科学的进步。折叠良好的标签可以溶解蛋白质。小的,未折叠的,肽样标签已经成为蛋白质纯化和蛋白质-蛋白质相互作用研究的宝贵工具。内在无序蛋白(IDPs)缺乏独特的三维结构,在过去十年中受到了指数级增长的关注。最近,大型ID标签已被开发用于溶解蛋白质和设计蛋白质和肽药物的药理学性质。在这里,我们对比了基于ID预测的折叠和ID标签的互补优势和应用。更少的结构通常意味着在更短的标签中有更多的功能。
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Ensemble descriptions of IDPs and IDRs: Integrating simulation and experiment Molecular mechanisms of fibrillation of IDPs Experimental studies of binding of intrinsically disordered proteins to their partners IDPs and IDRs in biomolecular condensates Index
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