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Crystallization and preliminary X-ray diffraction analysis of a specific VHH domain against mouse prion protein

Abskharon, R. N. N.
•
Soror, S. H.
•
Pardon, E.
altro
Wohlkonig, A.
2010
  • journal article

Periodico
ACTA CRYSTALLOGRAPHICA. SECTION F, STRUCTURAL BIOLOGY AND CRYSTALLIZATION COMMUNICATIONS
Abstract
Prion disorders are infectious diseases that are characterized by the conversion of the cellular prion protein PrPC into the pathogenic isoform PrPSc. Specific antibodies that interact with the cellular prion protein have been shown to inhibit this transition. Recombinant VHHs (variable domain of dromedary heavy-chain antibodies) or nanobodies are single-domain antibodies, making them the smallest antigen-binding fragments. A specific nanobody (Nb_PrP_01) was raised against mouse PrPC. A crystallization condition for this recombinant nanobody was identified using high-throughput screening. The crystals were optimized using streak-seeding and the hanging-drop method. The crystals belonged to the orthorhombic space group P2(1)2(1)2(1), with unit-cell parameters a=30.04, b=37.15, c=83.00 Å, and diffracted to 1.23 Å resolution using synchrotron radiation. The crystal structure of this specific nanobody against PrPC together with the known PrPC structure may help in understanding the PrPC/PrPSc transition mechanism.
DOI
10.1107/S1744309110042168
WOS
WOS:000285064800023
Archivio
http://hdl.handle.net/20.500.11767/14079
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-78650146355
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2998374/
Diritti
closed access
Soggetti
  • Camelidae

  • nanobodie

  • prion

  • PrPC

  • PrPSc

Scopus© citazioni
8
Data di acquisizione
Jun 2, 2022
Vedi dettagli
Web of Science© citazioni
8
Data di acquisizione
Mar 28, 2024
Visualizzazioni
2
Data di acquisizione
Apr 19, 2024
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