| Literature DB >> 25484214 |
Suresh Subedi1, Kristof Moonens1, Ema Romão2, Alvin Lo1, Guy Vandenbussche3, Jeanna Bugaytsova4, Serge Muyldermans2, Thomas Borén4, Han Remaut1.
Abstract
Helicobacter pylori is a human pathogen that colonizes about 50% of the world's population, causing chronic gastritis, duodenal ulcers and even gastric cancer. A steady emergence of multiple antibiotic resistant strains poses an important public health threat and there is an urgent requirement for alternative therapeutics. The blood group antigen-binding adhesin BabA mediates the intimate attachment to the host mucosa and forms a major candidate for novel vaccine and drug development. Here, the recombinant expression and crystallization of a soluble BabA truncation (BabA(25-460)) corresponding to the predicted extracellular adhesin domain of the protein are reported. X-ray diffraction data for nanobody-stabilized BabA(25-460) were collected to 2.25 Å resolution from a crystal that belonged to space group P21, with unit-cell parameters a = 50.96, b = 131.41, c = 123.40 Å, α = 90.0, β = 94.8, γ = 90.0°, and which was predicted to contain two BabA(25-460)-nanobody complexes per asymmetric unit.Entities:
Keywords: BabA; Helicobacter pylori; adhesin; nanobody
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Year: 2014 PMID: 25484214 PMCID: PMC4259228 DOI: 10.1107/S2053230X14023188
Source DB: PubMed Journal: Acta Crystallogr F Struct Biol Commun ISSN: 2053-230X Impact factor: 1.056