A dimorphism shift of hepatitis B virus capsids in response to ionic conditions. Issue 36 (5th September 2018)

• Record Type: Journal Article
• Authors: Sun, Xinyu; Li, Dong; Wang, Zhaoshuai; Liu, Qiao; Wei, Yinan; Liu, Tianbo
• Is Part Of: Nanoscale. Volume 10:Issue 36(2018)
• Page Start: 16984
• Page End: 16989
• Publication Date: 2018-09-05
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c8nr03370f
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : HBV capsid dimorphism regulation through manipulating the rate of capsid nucleation using highly concentrated and/or multivalent counter-cations. Abstract : The dimorphism of HBV capsids (coexistence of T = 3 and T = 4 capsids) was found to be regulatable by controlling the rate of capsid nucleation using cations such as K + or Ca 2+ : a quick addition of highly concentrated monovalent and/or multivalent counter-cations resulted in a morphism transition from a thermodynamically more stable, T = 4 capsid-dominant state (>80% of total capsids) to a new state containing ∼1 : 1 amounts of T = 3 and T = 4 capsids. These results suggested that the salts with strong charge screening ability could narrow the difference in nucleation energy barriers between the two states, which were not inter-convertible once formed. The effect of salts was more significant than other factors such as pH or protein concentration in achieving such a dimorphism shift. The general mechanism of HBV capsid dimorphism described here provides a new perspective in understanding the virus assembly during infection and directing the design of non-infectious capsids for nanotechnology applications.