Sponsor
The research was funded by the National Science Foundation (MCB 1715823 and MCB 2119837 to D.M.Z.) and (MCB 1617019 to E.B.) and the National Institutes of Health (R01GM141733 to D.M.Z. and E.B., F31EY033230 to R.M., R35GM124779 and R01EY030987 to S.L.R.).
Published In
Journal of Molecular Biology
Document Type
Pre-Print
Publication Date
3-1-2022
Subjects
Electron microscopy, Proteins -- Biology, Regulatory Proteins
Abstract
Multivalent intrinsically disordered protein (IDP) complexes are prevalent in biology and act in regulation of diverse processes, including transcription, signaling events, and the assembly and disassembly of complex macromolecular architectures. These systems pose significant challenges to structural investigation, due to continuum dynamics imparted by the IDP and compositional heterogeneity resulting from characteristic low-affinity interactions. Here, we developed a modular pipeline for automated single-particle electron microscopy (EM) distribution analysis of common but relatively understudied semi-ordered systems: 'beads-on-a-string' assemblies, composed of IDPs bound at multivalent sites to the ubiquitous ∼20kDacross-linking hub protein LC8. This approach quantifies conformational geometries and compositional heterogeneity on a single-particle basis, and statistically corrects spurious observations arising from random proximity of bound and unbound LC8. The statistical correction is generically applicable to oligomer characterization and not specific to our pipeline. Following validation, the approach was applied to the nuclear pore IDP Nup159 and the transcription factor ASCIZ. This analysis unveiled significant compositional and conformational diversity in both systems that could not be obtained from ensemble single particle EM class-averaging strategies, and new insights for exploring how these architectural properties might contribute to their physiological roles in supramolecular assembly and transcriptional regulation. We expect that this approach may be adopted to many other intrinsically disordered systems that have evaded traditional methods of structural characterization.
Locate the Document
DOI
10.1101/2020.06.16.154096
Persistent Identifier
https://archives.pdx.edu/ds/psu/37174
Citation Details
Published as: Mostofian, B., McFarland, R., Estelle, A., Howe, J., Barbar, E., Reichow, S. L., & Zuckerman, D. M. (2022). Continuum dynamics and statistical correction of compositional heterogeneity in multivalent IDP oligomers resolved by single-particle EM. Journal of Molecular Biology, 167520.
Description
This is the author’s version of a work. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document.