Laboratory of Organic Chemistry, ETH Zürich , 8093 Zürich, Switzerland.
J Am Chem Soc. 2015 Dec 30;137(51):16121-32. doi: 10.1021/jacs.5b10588. Epub 2015 Dec 17.
The engineered bacterial nanocompartment AaLS-13 is a promising artificial encapsulation system that exploits electrostatic interactions for cargo loading. In order to study its ability to take up and retain guests, a pair of fluorescent proteins was developed which allows spectroscopic determination of the extent of encapsulation by Förster resonance energy transfer (FRET). The encapsulation process is generally complete within a second, suggesting low energetic barriers for proteins to cross the capsid shell. Formation of intermediate aggregates upon mixing host and guest in vitro complicates capsid loading at low ionic strength, but can be sidestepped by increasing salt concentrations or diluting the components. Encapsulation of guests is completely reversible, and the position of the equilibrium is easily tuned by varying the ionic strength. These results, which challenge the notion that AaLS-13 is a continuous rigid shell, provide valuable information about cargo loading that will guide ongoing efforts to engineer functional host-guest complexes. Moreover, it should be possible to adapt the protein FRET pair described in this report to characterize functional capsid-cargo complexes generated by other encapsulation systems.
工程化细菌纳米隔室 AaLS-13 是一种很有前途的人工封装系统,利用静电相互作用进行货物装载。为了研究其摄取和保留客体的能力,开发了一对荧光蛋白,允许通过Förster 共振能量转移(FRET)光谱法确定封装的程度。封装过程通常在一秒内完成,这表明蛋白质穿过壳的能量壁垒较低。在体外混合宿主和客体时形成中间聚集体会使在低盐度下进行壳装载复杂化,但可以通过增加盐浓度或稀释成分来避免。客体的封装是完全可逆的,通过改变离子强度很容易调节平衡位置。这些结果挑战了 AaLS-13 是连续刚性壳的观点,提供了有关货物装载的有价值信息,这将指导设计功能性宿主-客体复合物的持续努力。此外,应该可以改编本报告中描述的蛋白质 FRET 对来表征其他封装系统生成的功能性壳-货物复合物。