Project goalIn Lipo-HANABI project, we need to develop the following two subsystems.
i) Sensing system (1st stage): liposome disruption by temperature control.
ii) Amplification system (2nd stage): a chain-reactive disruption of the liposomes activated by the 1st stage.
1st stage: Sensing systemThe purpose of 1st stage is to detect temperature change and release key molecules for the 2nd stage. This is achieved by temperature-sensitive liposomes containing the keys. To make the liposome, we used lipids conjugated with NIPAM polymer.
This structural change of NIPAM induces stress on the surface of the liposome, and consequently disrupts them.
Fig.1 Temperature-sensitive liposome
2nd stage: Amplification systemThe purpose of 2nd stage is to accept the key from the 1st stage and release a lot of payload molecules in a chain-reaction.
There are two different approaches to realize the 2nd stage.
A) DNA Origami approach
B) Flower DNA approach
DNA origami approachThis approach is inspired by a paper about Membrane-bending proteins (Prinz WA, Hinshaw JE., Crit Rev Biochem Mol Biol., 2009). In this approach, we use “Origami-anchor DNA” which connects DNA Origami with liposome membrane. A lot of DNA origamis are adsorbed on the surface of liposomes by using Origami-anchor DNA. DNA origami is supposed to be a stiff, straight board compared with liposome membrane, and as a result, liposome surface gets bending stress. At certain level of the absorbance, liposomes will burst. Also, DNA origamis on the surface repel each other because of negative charges on DNA backbones. This effect may add more stress on the membrane.
Fig.2 Stress on liposome membrane
From the reference, we learned that efficient structure design for destabilizing membranes should have the following properties:
DNA origami is known as a designable rigid structure made of DNA. We use DNA origami to make the rigid scaffolds. In order to meet the requirements, we designed a 2D rectangular DNA origami.
Fig.3 Rectangular origami
We use caDNAno2 for our DNA origami design. The size of DNA origami is 67.6nm (26 helixes) in width and 127 nm (374 bases) in height. We cut out a smaller rectangle of 10 helixes (161 bases) at one of the corners, so that we could distinguish the two sides with AFM (Atomic Force Microscope) observation. Also, we put 141 staples sticking out from the bottom face of the origami. Those staples hybridize with cholesterol-modified Origami-anchor DNA, which has high affinity with lipid membrane.
Fig.5 Unstable liposome
Flower DNA approachThis approach is inspired by a paper about Polymer Flower-micelle (Yukio Tominaga, Mari Mizuse, Akihito Hashidzume, Yotaro Morishima and Takahiro Sato, J. Phys. Chem. B, 2010).
To adapt the Polymer Flower-micelle to our project, the followings are required.
At first, we designed “Flower-anchor DNA”, which is a couple of ss DNAs both having cholesterol modified groups (Fig.6): Flower-anchor1 is 10nt ss DNA and Flower-anchor2 is 50nt ss DNA. Both are cholesterol-modified at their 3’ ends.
In addition, the 5’ end of the Flower-anchor2 is complementary to Flower-anchor1. When they hybridize, the rest 40nt of Flower-anchor2 remains single-stranded.
Fig.6 Liposome with Flower-anchor DNA
The key DNA released from stage 1 liposome is complementary to this single-stranded part. When the key hybridizes on it, a double-stranded section is formed. The length of the section is shorter than its persistence length; therefore it works as a rigid strut. The strut is anchored on the liposome at both ends, thus it extends the membrane. As a consequence, this may lead to drastic conformational change of the liposome, namely, disruption.
Fig.7 Process of flower DNA approach
Fig.8 How to disrupt a liposome