A Mutant Library Approach to Identify Improved Meningococcal Factor H Binding Protein Vaccine Antigens.

A Mutant Library Approach to Identify Improved Meningococcal Factor H Binding Protein Vaccine Antigens.
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DOI:
10.1371/journal.pone.0128185
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发表时间:
2015
期刊:
影响因子:
3.7
通讯作者:
Beernink PT
Beernink PT
中科院分区:
综合性期刊3区
文献类型:
--
作者:
Konar M;Rossi R;Walter H;Pajon R;Beernink PT

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Factor H binding protein (FHbp) is a virulence factor used by meningococci to evade the host complement system. FHbp elicits bactericidal antibodies in humans and is part of two recently licensed vaccines. Using human complement Factor H (FH) transgenic mice, we previously showed that binding of FH decreased the protective antibody responses to FHbp vaccination. Therefore, in the present study we devised a library-based method to identify mutant FHbp antigens with very low binding of FH. Using an FHbp sequence variant in one of the two licensed vaccines, we displayed an error-prone PCR mutant FHbp library on the surface of Escherichia coli. We used fluorescence-activated cell sorting to isolate FHbp mutants with very low binding of human FH and preserved binding of control anti-FHbp monoclonal antibodies. We sequenced the gene encoding FHbp from selected clones and introduced the mutations into a soluble FHbp construct. Using this approach, we identified several new mutant FHbp vaccine antigens that had very low binding of FH as measured by ELISA and surface plasmon resonance. The new mutant FHbp antigens elicited protective antibody responses in human FH transgenic mice that were up to 20-fold higher than those elicited by the wild-type FHbp antigen. This approach offers the potential to discover mutant antigens that might not be predictable even with protein structural information and potentially can be applied to other microbial vaccine antigens that bind host proteins.
DOI: 10.1097/coh.0b013e3283632c26
发表时间: 2013-09
影响因子: 4.1
作者:
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DOI: 10.1093/infdis/jit239
发表时间: 2013-08-15
期刊: The Journal of infectious diseases
影响因子: --
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期刊: VACCINE
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DOI: 10.1086/597806
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