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2XTL

Structure of the major pilus backbone protein from Streptococcus Agalactiae

Summary for 2XTL
Entry DOI10.2210/pdb2xtl/pdb
DescriptorCELL WALL SURFACE ANCHOR FAMILY PROTEIN, POTASSIUM ION (3 entities in total)
Functional Keywordsgram-positive pili protein, bp-2a 515 allele, immunoglobulin-like domains, structural protein
Biological sourceSTREPTOCOCCUS AGALACTIAE
Total number of polymer chains2
Total formula weight98943.15
Authors
Rinauda, D.,Gourlay, L.J.,Soriano, M.,Grandi, G.,Bolognesi, M. (deposition date: 2010-10-11, release date: 2011-07-06, Last modification date: 2024-10-23)
Primary citationNuccitelli, A.,Cozzi, R.,Gourlay, L.J.,Donnarumma, D.,Necchi, F.,Norais, N.,Telford, J.L.,Rappuoli, R.,Bolognesi, M.,Maione, D.,Grandi, G.,Rinaudo, C.D.
Structure-Based Approach to Rationally Design a Chimeric Protein for an Effective Vaccine Against Group B Streptococcus Infections.
Proc.Natl.Acad.Sci.USA, 108:10278-, 2011
Cited by
PubMed Abstract: Structural vaccinology is an emerging strategy for the rational design of vaccine candidates. We successfully applied structural vaccinology to design a fully synthetic protein with multivalent protection activity. In Group B Streptococcus, cell-surface pili have aroused great interest because of their direct roles in virulence and importance as protective antigens. The backbone subunit of type 2a pilus (BP-2a) is present in six immunogenically different but structurally similar variants. We determined the 3D structure of one of the variants, and experimentally demonstrated that protective antibodies specifically recognize one of the four domains that comprise the protein. We therefore constructed a synthetic protein constituted by the protective domain of each one of the six variants and showed that the chimeric protein protects mice against the challenge with all of the type 2a pilus-carrying strains. This work demonstrates the power of structural vaccinology and will facilitate the development of an optimized, broadly protective pilus-based vaccine against Group B Streptococcus by combining the uniquely generated chimeric protein with protective pilin subunits from two other previously identified pilus types. In addition, this work describes a template procedure that can be followed to develop vaccines against other bacterial pathogens.
PubMed: 21593422
DOI: 10.1073/PNAS.1106590108
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.75 Å)
Structure validation

238895

数据于2025-07-16公开中

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