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Nanobody-aided crystallization of the transcription regulator PaaR2 from Escherichia coli O157:H7.


ABSTRACT: paaR2-paaA2-parE2 is a three-component toxin-antitoxin module found in prophage CP-993P of Escherichia coli O157:H7. Transcription regulation of this module occurs via the 123-amino-acid regulator PaaR2, which forms a large oligomeric structure. Despite appearing to be well folded, PaaR2 withstands crystallization, as does its N-terminal DNA-binding domain. Native mass spectrometry was used to screen for nanobodies that form a unique complex and stabilize the octameric structure of PaaR2. One such nanobody, Nb33, allowed crystallization of the protein. The resulting crystals belong to space group F432, with unit-cell parameter a = 317 Å, diffract to 4.0 Å resolution and are likely to contain four PaaR2 monomers and four nanobody monomers in the asymmetric unit. Crystals of two truncates containing the N-terminal helix-turn-helix domain also interact with Nb33, and the corresponding co-crystals diffracted to 1.6 and 1.75 Å resolution.

SUBMITTER: De Bruyn P 

PROVIDER: S-EPMC8488858 | biostudies-literature | 2021 Oct

REPOSITORIES: biostudies-literature

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Nanobody-aided crystallization of the transcription regulator PaaR2 from Escherichia coli O157:H7.

De Bruyn Pieter P   Prolič-Kalinšek Maruša M   Vandervelde Alexandra A   Malfait Milan M   Sterckx Yann G J YGJ   Sobott Frank F   Hadži San S   Pardon Els E   Steyaert Jan J   Loris Remy R  

Acta crystallographica. Section F, Structural biology communications 20210921 Pt 10


paaR2-paaA2-parE2 is a three-component toxin-antitoxin module found in prophage CP-993P of Escherichia coli O157:H7. Transcription regulation of this module occurs via the 123-amino-acid regulator PaaR2, which forms a large oligomeric structure. Despite appearing to be well folded, PaaR2 withstands crystallization, as does its N-terminal DNA-binding domain. Native mass spectrometry was used to screen for nanobodies that form a unique complex and stabilize the octameric structure of PaaR2. One su  ...[more]

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