Unknown

Dataset Information

0

Terminal modifications of norovirus P domain resulted in a new type of subviral particles, the small P particles.


ABSTRACT: The protruding (P) domain of norovirus VP1 is responsible for immune recognition and host receptor interaction. Our previous studies have demonstrated that a modification of the ends of the P domain affects the conformation and/or function of the P protein. An expression of the P domain with or without the hinge, or with an additional cysteine at either ends of the P protein resulted in P dimers and/or P particles. Here we report a new type of subviral particle, the small P particles, through a further modification, either an addition of the flag tag or a change of the arginine cluster, at the C-terminus of the cysteine-containing P domain. Gel filtration and cryo-EM studies showed that the small P particles are tetrahedrons formed by 6 P dimers or 12 P monomers that is half-size of the P particles. Fitting of the crystal structure of the P domain into the cryo-EM density map of the particle indicated similar conformations of the P dimers as those in P particles. The small P particles bind human HBGAs and are antigenically reactive similar to their parental VLPs and P particles. These data suggest that the C-terminus of the P domain is an important factor in the formation of the P particles. Further elucidation of the mechanism of these modifications in the P particle formation would be important in structure biology and morphogenesis of noroviruses. The small P particles may also be a useful alternative in study of norovirus-host interaction and vaccine development for noroviruses.

SUBMITTER: Tan M 

PROVIDER: S-EPMC3064930 | biostudies-literature | 2011 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Terminal modifications of norovirus P domain resulted in a new type of subviral particles, the small P particles.

Tan Ming M   Fang Ping-An PA   Xia Ming M   Chachiyo Teepanis T   Jiang Wen W   Jiang Xi X  

Virology 20101223 2


The protruding (P) domain of norovirus VP1 is responsible for immune recognition and host receptor interaction. Our previous studies have demonstrated that a modification of the ends of the P domain affects the conformation and/or function of the P protein. An expression of the P domain with or without the hinge, or with an additional cysteine at either ends of the P protein resulted in P dimers and/or P particles. Here we report a new type of subviral particle, the small P particles, through a  ...[more]

Similar Datasets

| S-EPMC4586464 | biostudies-literature
| S-EPMC9355357 | biostudies-literature
| S-EPMC7824077 | biostudies-literature
2021-01-11 | PXD023182 | Pride
| S-EPMC5476370 | biostudies-literature
| S-EPMC150630 | biostudies-literature
| S-EPMC8103704 | biostudies-literature
| S-EPMC7281111 | biostudies-literature
| S-EPMC6895789 | biostudies-literature
| S-EPMC229348 | biostudies-literature