The Position of His-Tag in Recombinant OspC and Application of Various Adjuvants Affects the Intensity and Quality of Specific Antibody Response after Immunization of Experimental Mice
Jazyk angličtina Země Spojené státy americké Médium electronic-ecollection
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26848589
PubMed Central
PMC4744052
DOI
10.1371/journal.pone.0148497
PII: PONE-D-15-48677
Knihovny.cz E-zdroje
- MeSH
- adjuvancia imunologická * MeSH
- antigeny bakteriální aplikace a dávkování chemie imunologie MeSH
- Borrelia burgdorferi imunologie MeSH
- ELISA MeSH
- imunizace MeSH
- lymeská nemoc imunologie MeSH
- modely u zvířat MeSH
- myši MeSH
- proteiny vnější bakteriální membrány aplikace a dávkování chemie imunologie MeSH
- proteolipidy MeSH
- protilátky bakteriální imunologie MeSH
- rekombinantní fúzní proteiny aplikace a dávkování chemie imunologie izolace a purifikace MeSH
- sekundární struktura proteinů MeSH
- specificita protilátek imunologie MeSH
- stabilita proteinů MeSH
- tvorba protilátek imunologie MeSH
- zvířata MeSH
- Check Tag
- myši MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- adjuvancia imunologická * MeSH
- antigeny bakteriální MeSH
- OspC protein MeSH Prohlížeč
- proteiny vnější bakteriální membrány MeSH
- proteolipidy MeSH
- proteoliposomes MeSH Prohlížeč
- protilátky bakteriální MeSH
- rekombinantní fúzní proteiny MeSH
Lyme disease, Borrelia burgdorferi-caused infection, if not recognized and appropriately treated by antibiotics, may lead to chronic complications, thus stressing the need for protective vaccine development. The immune protection is mediated by phagocytic cells and by Borrelia-specific complement-activating antibodies, associated with the Th1 immune response. Surface antigen OspC is involved in Borrelia spreading through the host body. Previously we reported that recombinant histidine tagged (His-tag) OspC (rOspC) could be attached onto liposome surfaces by metallochelation. Here we report that levels of OspC-specific antibodies vary substantially depending upon whether rOspC possesses an N' or C' terminal His-tag. This is the case in mice immunized: (a) with rOspC proteoliposomes containing adjuvants MPLA or non-pyrogenic MDP analogue MT06; (b) with free rOspC and Montanide PET GEL A; (c) with free rOspC and alum; or (d) with adjuvant-free rOspC. Stronger responses are noted with all N'-terminal His-tag rOspC formulations. OspC-specific Th1-type antibodies predominate post-immunization with rOspC proteoliposomes formulated with MPLA or MT06 adjuvants. Further analyses confirmed that the structural features of soluble N' and C' terminal His-tag rOspC and respective rOspC proteoliposomes are similar including their thermal stabilities at physiological temperatures. On the other hand, a change in the position of the rOspC His-tag from N' to C' terminal appears to affect substantially the immunogenicity of rOspC arguably due to steric hindrance of OspC epitopes by the C' terminal His-tag itself and not due to differences in overall conformations induced by changes in the His-tag position in rOspC variants.
Apigenex Prague Czech Republic
Department of Pharmacology and Immunotherapy Veterinary Research Institute Brno Czech Republic
International Clinical Research Center St Anne´s University Hospital Brno Czech Republic
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