» Articles » PMID: 31585705

NMR Mapping of Disordered Segments from a Viral Scaffolding Protein Enclosed in a 23 MDa Procapsid

Overview
Journal Biophys J
Publisher Cell Press
Specialty Biophysics
Date 2019 Oct 6
PMID 31585705
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Scaffolding proteins (SPs) are required for the capsid shell assembly of many tailed double-stranded DNA bacteriophages, some archaeal viruses, herpesviruses, and adenoviruses. Despite their importance, only one high-resolution structure is available for SPs within procapsids. Here, we use the inherent size limit of NMR to identify mobile segments of the 303-residue phage P22 SP free in solution and when incorporated into a ∼23 MDa procapsid complex. Free SP gives NMR signals from its acidic N-terminus (residues 1-40) and basic C-terminus (residues 264-303), whereas NMR signals from the middle segment (residues 41-263) are missing because of intermediate conformational exchange on the NMR chemical shift timescale. When SP is incorporated into P22 procapsids, NMR signals from the C-terminal helix-turn-helix domain disappear because of binding to the procapsid interior. Signals from the N-terminal domain persist, indicating that this segment retains flexibility when bound to procapsids. The unstructured character of the N-terminus, coupled with its high content of negative charges, is likely important for dissociation and release of SP during the double-stranded DNA genome packaging step accompanying phage maturation.

Citing Articles

Visualizing liquid-liquid phase transitions.

Sahoo B, Deng X, Wong E, Clark N, Yang H, Subramanian V bioRxiv. 2024; .

PMID: 39554013 PMC: 11565804. DOI: 10.1101/2023.10.09.561572.


Characterization of Intrinsically Disordered Proteins in Healthy and Diseased States by Nuclear Magnetic Resonance.

Shahrajabian M, Sun W Rev Recent Clin Trials. 2024; 19(3):176-188.

PMID: 38409704 DOI: 10.2174/0115748871271420240213064251.


Pulse-field gradient nuclear magnetic resonance of protein translational diffusion from native to non-native states.

Whitehead 3rd R, Teschke C, Alexandrescu A Protein Sci. 2022; 31(5):e4321.

PMID: 35481638 PMC: 9047038. DOI: 10.1002/pro.4321.


NMR as a "Gold Standard" Method in Drug Design and Discovery.

Emwas A, Szczepski K, Poulson B, Chandra K, McKay R, Dhahri M Molecules. 2020; 25(20).

PMID: 33050240 PMC: 7594251. DOI: 10.3390/molecules25204597.

References
1.
Israel V . E proteins of bacteriophage P22. I. Identification and ejection from wild-type and defective particles. J Virol. 1977; 23(1):91-7. PMC: 515803. DOI: 10.1128/JVI.23.1.91-97.1977. View

2.
Weigele P, Sampson L, Winn-Stapley D, Casjens S . Molecular genetics of bacteriophage P22 scaffolding protein's functional domains. J Mol Biol. 2005; 348(4):831-44. DOI: 10.1016/j.jmb.2005.03.004. View

3.
Parent K, Khayat R, Tu L, Suhanovsky M, Cortines J, Teschke C . P22 coat protein structures reveal a novel mechanism for capsid maturation: stability without auxiliary proteins or chemical crosslinks. Structure. 2010; 18(3):390-401. PMC: 2951021. DOI: 10.1016/j.str.2009.12.014. View

4.
Fane B, Prevelige Jr P . Mechanism of scaffolding-assisted viral assembly. Adv Protein Chem. 2003; 64:259-99. DOI: 10.1016/s0065-3233(03)01007-6. View

5.
Cortines J, Weigele P, Gilcrease E, Casjens S, Teschke C . Decoding bacteriophage P22 assembly: identification of two charged residues in scaffolding protein responsible for coat protein interaction. Virology. 2011; 421(1):1-11. PMC: 3208733. DOI: 10.1016/j.virol.2011.09.005. View