Summary of viral replication kinetics, nuclear localization, nuclear export capacity, and CRM1 binding of the NP-NES3 consensus sequence mutants.

a% virus titer ± SD compared with WT at the 46 h of replication kinetic assay from the Fig. 4C.
bNo viral rescue by reverse genetics.
c% cell count ± SD with nuclear localization of NP from the Fig. 5B.
d−, ±, + indicate not occur, partially occur, occur of nuclear export capacity, respectively derived from the Fig. 6.
e% intensity of the pull-downed NP band compared with WT from the Fig. 7C.

a. 相对于野生型（Wild Type, WT）的病毒滴度（virus titer）百分比±标准差（SD），为复制动力学实验中培养46小时的检测结果，数据对应图4C。
b. 未通过反向遗传学技术实现病毒拯救。
c. 具有NP蛋白核定位特征的细胞占比±标准差（SD），数据对应图5B。
d. 符号−、±、+分别代表核输出能力未发生、部分发生及完全发生，数据对应图6。
e. 免疫沉淀富集的NP蛋白条带信号强度占野生型（Wild Type, WT）的百分比，数据对应图7C。