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蛋白质固有无序的生物物理和综合特征作为药物发现的主要靶点。

Biophysical and Integrative Characterization of Protein Intrinsic Disorder as a Prime Target for Drug Discovery.

机构信息

Center for Proteomics and Department of Nutrition, School of Medicine, Case Western Reserve University, Cleveland, OH 44106, USA.

Department of Physics, Arizona State University, Tempe, AZ 85287, USA.

出版信息

Biomolecules. 2023 Mar 14;13(3):530. doi: 10.3390/biom13030530.

Abstract

Protein intrinsic disorder is increasingly recognized for its biological and disease-driven functions. However, it represents significant challenges for biophysical studies due to its high conformational flexibility. In addressing these challenges, we highlight the complementary and distinct capabilities of a range of experimental and computational methods and further describe integrative strategies available for combining these techniques. Integrative biophysics methods provide valuable insights into the sequence-structure-function relationship of disordered proteins, setting the stage for protein intrinsic disorder to become a promising target for drug discovery. Finally, we briefly summarize recent advances in the development of new small molecule inhibitors targeting the disordered N-terminal domains of three vital transcription factors.

摘要

蛋白质内无序结构因其在生物学和疾病驱动功能方面的作用而受到越来越多的关注。然而,由于其高度的构象灵活性,它给生物物理研究带来了重大挑战。在解决这些挑战的过程中,我们强调了一系列实验和计算方法的互补和独特功能,并进一步描述了可用于结合这些技术的综合策略。综合生物物理学方法为研究无序蛋白质的序列-结构-功能关系提供了有价值的见解,为将蛋白质内无序结构作为药物发现的有前途的靶点奠定了基础。最后,我们简要总结了最近在开发针对三种重要转录因子无规则 N 端结构域的新型小分子抑制剂方面的进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b66b/10046839/e449607ad6a0/biomolecules-13-00530-g001.jpg

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