摘要: Linear artificial viruses (AVs) can be formed through a self-assembly process which is strongly influenced by assembly signals on their genetic material. In this thesis the description of with multiple and variable nucleation cost assessed. It shows that combination two determines in regime is. An signal, position entropy dominated distinguished. Furthermore, zipper an account given kinetics finite as opposed to infinite protein concentration. Finite concentration gives rise overshoots undershoots. Finally, for self-competing system universal curve valuable tool determining strength signal from measurements.
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