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

Author:

Luo Shuqi1,Wohl Samuel2,Zheng Wenwei3,Yang Sichun14ORCID

Affiliation:

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

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

3. College of Integrative Sciences and Arts, Arizona State University, Mesa, AZ 85212, USA

4. Case Comprehensive Cancer Center, Case Western Reserve University, Cleveland, OH 44106, USA

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.

Funder

the National Institutes of Health

NCI

National Science Foundation

Publisher

MDPI AG

Subject

Molecular Biology,Biochemistry

Reference307 articles.

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3. Structural analysis of intrinsically disordered proteins by small-angle X-ray scattering;Bernado;Mol. Biosyst.,2012

4. Random-coil behavior and the dimensions of chemically unfolded proteins;Kohn;Proc. Natl. Acad. Sci. USA,2004

5. Flory, P.J. (1953). Principles of Polymer Chemistry, Cornell University Press.

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