This paper presents the development and hovering control of a tailsitter unmanned aerial vehicle (UAV) that merges long endurance and vertical takeoff and landing (VTOL) abilities. The designed tailsitter contains one flying-wing with two motors and two elevons. Vehicle aerodynamics and a six-degrees-of-freedom (6-DOF) model are especially developed for the tailsitter. To achieve a good performance in outdoor stationary hovering and accurate vertical flying, the active disturbance rejection control (ADRC) for attitude controller is proposed. With signals from extended state observer (ESO) and tracking differentiator (TD), ADRC decouples the system model into a controllable chain of integrators. Based on the decoupled system dynamics, the motion of tailsitter can be easily handled by developed position controller. Experimental results are presented to corroborate the effectiveness of the controller in disturbance rejection.
Zika virus (ZIKV) is an RNA-enveloped virus that belongs to the Flavivirus genus, and ZIKV infections potentially induce severe neurodegenerative diseases and impair male fertility. Palmitoylation is an important post-translational modification of proteins that is mediated by a series of DHHC-palmitoyl transferases, which are implicated in various biological processes and viral infections. However, it remains to be investigated whether palmitoylation regulates ZIKV infections. In this study, we initially observed that the inhibition of palmitoylation by 2-bromopalmitate (2-BP) enhanced ZIKV infections, and determined that the envelope protein of ZIKV is palmitoylated at Cys308. ZDHHC11 was identified as the predominant enzyme that interacts with the ZIKV envelope protein and catalyzes its palmitoylation. Notably, ZDHHC11 suppressed ZIKV infections in an enzymatic activity-dependent manner and ZDHHC11 knockdown promoted ZIKV infection. In conclusion, we proposed that the envelope protein of ZIKV undergoes a novel post-translational modification and identified a distinct mechanism in which ZDHHC11 suppresses ZIKV infections via palmitoylation of the ZIKV envelope protein.