Chikungunya virus (CHIKV) is a mosquito-borne virus， which has created an alarming threat in the world due to unavailability of vaccine and antiviral compounds. The CHIKV nsP2 contains ATPase， RTPase， helicase and protease activities， whereas， nsP1 is a viral capping enzyme. In alphaviruses， the four non-structural proteins form the replication complex in the cytoplasm and this study characterizes the interaction between CHIKV nsP1 and nsP2. It was observed that， both the proteins co-localize in the cytoplasm and interact in the CHIKV infected cells by confocal microscopy and immunoprecipitation assay. Further， it was demonstrated through mutational analysis that， the amino acids 1-95 of nsP2 ... More
Chikungunya virus (CHIKV) is a mosquito-borne virus， which has created an alarming threat in the world due to unavailability of vaccine and antiviral compounds. The CHIKV nsP2 contains ATPase， RTPase， helicase and protease activities， whereas， nsP1 is a viral capping enzyme. In alphaviruses， the four non-structural proteins form the replication complex in the cytoplasm and this study characterizes the interaction between CHIKV nsP1 and nsP2. It was observed that， both the proteins co-localize in the cytoplasm and interact in the CHIKV infected cells by confocal microscopy and immunoprecipitation assay. Further， it was demonstrated through mutational analysis that， the amino acids 1-95 of nsP2 and 170-288 of nsP1 are responsible for their direct interaction. Additionally， it was noticed that， the ATPase activity of nsP2 is enhanced in the presence of nsP1， indicating the functional significance of this interaction. In silico analysis showed close (≤1.7 Å) polar interaction (hydrogen bond) between Glu， Arg of nsP2 with Lys， Val and Phe of nsP1 respectively. Hence， this investigation provides molecular characterization of CHIKV nsP1-nsP2 interaction which might be a useful target for rational designing of antiviral drugs.
