Table 2.
Summary of technical details in different CFPS system. Citations indicate where more information about the systems in the context of cell-free can be found.
| Physical signal | Key elements | Cell-free system | Reaction format | Volume | Pros | Cons | Ref. |
|---|---|---|---|---|---|---|---|
| Light | YF1/FixJ | E. coli extract | Batch; One compartment |
20 μL | Abundant components responding to different wavelengths | Slow signal relay and reversal rates; Poor portability |
[5] |
| EL222 | E. coli extract | Batch; One compartment |
25 μL | Good portability; Fast response |
Limited response wavelength | [17] | |
| Azobenzene-tethered promoter | PURE | Batch; One compartment |
– | Avoiding complex protein interactions | Tedious preparation process | [30] | |
| Temperature | RNAT | PURE | Batch; One compartment |
– | Flexible and varied means of temperature control | Low expression | [18] |
| Electric field | DNA brush on a chip | PURE | Batch; Fixed in compartment on a chip |
Compartment: R = 35 μm; H = 3 μm |
Novel manipulation of cell-free expression | Reduced component performance by electrothermal effect | [19] |
| DMF board | E. coli extract | Batch; Multiple droplet compartments |
20 μL | Remoted control of cell-free expression | Limited control scale | [42] | |
| Magnetic force | Magnetic beads coated with DNAs | E. coli extract | Batch; One compartment |
24 μL | Simple control method and spatiotemporal principle | The attachment effectiveness of DNA on magnetic beads | [20] |