Crystal structure of c5321: a protective antigen present in uropathogenic Escherichia coli strains displaying an SLR foldReportar como inadecuado




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BMC Structural Biology

, 13:19

Crystallography

Abstract

BackgroundIncreasing rates of antimicrobial resistance among uropathogens led, among other efforts, to the application of subtractive reverse vaccinology for the identification of antigens present in extraintestinal pathogenic E. coli ExPEC strains but absent or variable in non-pathogenic strains, in a quest for a broadly protective Escherichia coli vaccine. The protein coded by locus c5321 from CFT073 E. coli was identified as one of nine potential vaccine candidates against ExPEC and was able to confer protection with an efficacy of 33% in a mouse model of sepsis. c5321 known also as EsiB lacks functional annotation and structurally belongs to the Sel1-like repeat SLR family. Herein, as part of the general characterization of this potential antigen, we have focused on its structural properties.

ResultsWe report the 1.74 Å-resolution crystal structure of c5321 from CFT073 E. coli determined by Se-Met SAD phasing. The structure is composed of 11 SLR units in a topological organisation that highly resembles that found in HcpC from Helicobacter pylori, with the main difference residing in how the super-helical fold is stabilised. The stabilising effect of disulfide bridges in HcpC is replaced in c5321 by a strengthening of the inter-repeat hydrophobic core. A metal-ion binding site, uncharacteristic of SLR proteins, is detected between SLR units 3 and 4 in the region of the inter-repeat hydrophobic core. Crystal contacts are observed between the C-terminal tail of one molecule and the C-terminal amphipathic groove of a neighbouring one, resembling interactions between ligand and proteins containing tetratricopeptide-like repeats.

ConclusionsThe structure of antigen c5321 presents a mode of stabilization of the SLR fold different from that observed in close homologs of known structure. The location of the metal-ion binding site and the observed crystal contacts suggest a potential role in regulation of conformational flexibility and interaction with yet unidentified target proteins, respectively. These findings open new perspectives in both antigen design and for the identification of a functional role for this protective antigen.

Keywordsc5321 Sel1-like repeat Crystal structure Super-helical fold Antigen Uropathogenic Escherichia coli Electronic supplementary materialThe online version of this article doi:10.1186-1472-6807-13-19 contains supplementary material, which is available to authorized users.

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Autor: Dunja Urosev - Mario Ferrer-Navarro - Ilaria Pastorello - Elena Cartocci - Lionel Costenaro - Dmitrijs Zhulenkovs - Jean-Did

Fuente: https://link.springer.com/







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