Team:Penn/LightActivatedLysis

We then wanted to prove that our pDawn-ClyA construct was able to lyse mammalian cells in a light-dependent manner. To assess this, we plated BL21 bacteria transformed with pDawn-ClyA or pDawn-mCherry on Columbia Agar plates supplemented with 5% sheep blood (BD). These plates are used to qualitatively detect hemolytic activity in bacteria by visually confirming lysis through a color change in the media as the blood cells are lysed. After plating the bacteria, cultures were grown in non-inducing conditions at 37°C until visible colonies were present (~12 hours). Plates were then grown at 25°C under either inducing or non-inducing conditions for 24 hours and imaged. These results are visible in Figure 4.

pDawn-mCherry Dark

pDawn-mCherry Light

pDawn-His-ClyA Dark

pDawn-His-ClyA Light

Since our goal is a system for drug delivery, it is especially important to show spatial control of lysis. The advantage of our light-based system is the precision gained through using light to selectively target regions of the body to kill cells. We tested this concept on our blood agar plates by selectively exposing half of the plates to light conditions and the other half to dark conditions. Shown below in Figure 4, only the region exposed to lightshows cell lysis. Similarly, when we plated a fun pattern in Figure 5, only the bottom half exposed to light shows cell lysis. There is little leakage that can be seen in these plates indicating the high degree of control which our system provides

Figure 5
Figure 5: Colony Spatial Control.

Figure 6
Figure 6: Penn iGEM spatial control