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4L8I

Crystal structure of RSV epitope scaffold FFL_005

Summary for 4L8I
Entry DOI10.2210/pdb4l8i/pdb
DescriptorRSV epitope scaffold FFL_005 (2 entities in total)
Functional Keywordsthree-helix bundle, immune system
Biological sourcesynthetic construct
Total number of polymer chains2
Total formula weight27419.51
Authors
Jardine, J.,Correnti, C.,Holmes, M.A.,Strong, R.K.,Schief, W.R. (deposition date: 2013-06-17, release date: 2014-02-12, Last modification date: 2024-02-28)
Primary citationCorreia, B.E.,Bates, J.T.,Loomis, R.J.,Baneyx, G.,Carrico, C.,Jardine, J.G.,Rupert, P.,Correnti, C.,Kalyuzhniy, O.,Vittal, V.,Connell, M.J.,Stevens, E.,Schroeter, A.,Chen, M.,Macpherson, S.,Serra, A.M.,Adachi, Y.,Holmes, M.A.,Li, Y.,Klevit, R.E.,Graham, B.S.,Wyatt, R.T.,Baker, D.,Strong, R.K.,Crowe, J.E.,Johnson, P.R.,Schief, W.R.
Proof of principle for epitope-focused vaccine design.
Nature, 507:201-206, 2014
Cited by
PubMed Abstract: Vaccines prevent infectious disease largely by inducing protective neutralizing antibodies against vulnerable epitopes. Several major pathogens have resisted traditional vaccine development, although vulnerable epitopes targeted by neutralizing antibodies have been identified for several such cases. Hence, new vaccine design methods to induce epitope-specific neutralizing antibodies are needed. Here we show, with a neutralization epitope from respiratory syncytial virus, that computational protein design can generate small, thermally and conformationally stable protein scaffolds that accurately mimic the viral epitope structure and induce potent neutralizing antibodies. These scaffolds represent promising leads for the research and development of a human respiratory syncytial virus vaccine needed to protect infants, young children and the elderly. More generally, the results provide proof of principle for epitope-focused and scaffold-based vaccine design, and encourage the evaluation and further development of these strategies for a variety of other vaccine targets, including antigenically highly variable pathogens such as human immunodeficiency virus and influenza.
PubMed: 24499818
DOI: 10.1038/nature12966
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2 Å)
Structure validation

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