FEBS Letters | |
Mosaic Qβ coats as a new presentation model | |
Pumpens, Paul1  Strelnikova, Anna1  Ose, Velta1  Cielens, Indulis1  Vasiljeva, Inta1  Kazaks, Andris1  Kozlovska, Tatjana1  | |
[1] Biomedical Research and Study Centre, University of Latvia, Ratsupites Str. 1, Riga, Latvia | |
关键词: Phage Qβ; Coat protein UGA suppression; A1 extension; Capsid assembly; Hepatitis B virus preS1; Immunogenicity; | |
DOI : 10.1016/S0014-5793(98)00716-9 | |
学科分类:生物化学/生物物理 | |
来源: John Wiley & Sons Ltd. | |
【 摘 要 】
The new protein carrier was developed on the basis of recombinant RNA phage Qβ capsid. C-terminal UGA extension of the short form of Qβ coat, so-called A1 extension, served as a target for presentation of foreign peptides on the outer surface of mosaic Qβ particles. In conditions of enhanced UGA suppression, the proportion of A1-extended to short coats in mosaic particles dropped from 48% to 14%, with an increase of the length of A1 extension. A model insertion, short preS1 epitope 31-DPAFR-35 of hepatitis B surface antigen, demonstrated superficial location on the mosaic Qβ particles and ensured specific antigenicity and immunogenicity.
【 授权许可】
Unknown
【 预 览 】
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RO201912020306191ZK.pdf | 528KB | download |