Single-molecule fluorescence studies of intrinsically disordered proteins and liquid phase separation
Review article, 2019

Intrinsically disordered proteins (IDPs) are ubiquitous in proteomes and serve in a range of cellular functions including signaling, regulation, transport and enzyme function. IDP misfunction and aggregation are also associated with several diseases including neurodegenerative diseases and cancer. During the past decade, single-molecule methods have become popular for detailed biophysical and structural studies of these complex proteins. This work has included recent applications to cellular liquid-liquid phase separation (LLPS), relevant for functional dynamics of membraneless organelles such as the nucleolus and stress granules. In this concise review, we cover the conceptual motivations for development and application of single-molecule fluorescence methods for such IDP studies. We follow with a few key examples of systems and biophysical problems that have been addressed, and conclude with thoughts for emerging and future directions.

Single-molecule biophysics

Intrinsically disordered proteins

Single-molecule FRET

Liquid-liquid phase separation

Author

Irem Nasir

Scripps Research Institute

Chalmers, Biology and Biological Engineering, Chemical Biology

Paulo L. Onuchic

Scripps Research Institute

Sergio R. Labra

Scripps Research Institute

Ashok A. Deniz

Scripps Research Institute

Biochimica et Biophysica Acta - Proteins and Proteomics

1570-9639 (ISSN) 18781454 (eISSN)

Vol. 1867 10 980-987

Subject Categories

Biochemistry and Molecular Biology

Biophysics

Medical Biotechnology (with a focus on Cell Biology (including Stem Cell Biology), Molecular Biology, Microbiology, Biochemistry or Biopharmacy)

DOI

10.1016/j.bbapap.2019.04.007

PubMed

31054969

More information

Latest update

5/19/2021