Human coronavirus (HCoV) NL63 was first described in 2004 and is associated with respiratory tract disease of varying severity. At the genetic and structural level, HCoV-NL63 is similar to other members of the Coronavirinae subfamily, especially human coronavirus 229E (HCoV-229E). Detailed analysis, however, reveals several unique features of the pathogen. The coronaviral nucleocapsid protein is abundantly present in infected cells. It is a multi-domain, multi-functional protein important for viral replication and a number of cellular processes. The aim of the present study was to characterize the HCoV-NL63 nucleocapsid protein. Biochemical analyses revealed that the protein shares characteristics with homologous proteins encoded in other coronaviral genomes, with the N-terminal domain responsible for nucleic acid binding and the C-terminal domain involved in protein oligomerization. Surprisingly, analysis of the subcellular localization of the N protein of HCoV-NL63 revealed that, differently than homologous proteins from other coronaviral species except for SARS-CoV, it is not present in the nucleus of infected or transfected cells. Furthermore, no significant alteration in cell cycle progression in cells expressing the protein was observed. This is in stark contrast with results obtained for other coronaviruses, except for the SARS-CoV.
The nucleocapsid protein of human coronavirus NL63.
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作者:ZuwaÅa Kaja, Golda Anna, Kabala Wojciech, Burmistrz MichaÅ, Zdzalik Michal, Nowak Paulina, Kedracka-Krok Sylwia, Zarebski MirosÅaw, Dobrucki Jerzy, Florek Dominik, Zeglen SÅawomir, Wojarski Jacek, Potempa Jan, Dubin Grzegorz, Pyrc Krzysztof
| 期刊: | PLoS One | 影响因子: | 2.600 |
| 时间: | 2015 | 起止号: | 2015 Feb 20; 10(2):e0117833 |
| doi: | 10.1371/journal.pone.0117833 | ||
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