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Presented here are protocols for the creation of peptide-based small unilamellar vesicles capable of growth. To facilitate in vesiculo production of the membrane peptide, these vesicles are equipped with a transcription-translation system and the peptide-encoding plasmid.
Compartmentalization of biochemical reactions is a central aspect of synthetic cells. For this purpose, peptide-based reaction compartments serve as an attractive alternative to liposomes or fatty acid-based vesicles. Externally or within the vesicles, peptides can be easily expressed and simplify the synthesis of membrane precursors. Provided here is a protocol for the creation of vesicles with diameters of ~200 nm based on the amphiphilic elastin-like polypeptides (ELP) utilizing dehydration-rehydration from glass beads. Also presented are protocols for bacterial ELP expression and purification via inverse temperature cycling, as well as their covalent functionalization with fluorescent dyes. Furthermore, this report describes a protocol to enable the transcription of RNA aptamer dBroccoli inside ELP vesicles as a less complex example for a biochemical reaction. Finally, a protocol is provided, which allows in vesiculo expression of fluorescent proteins and the membrane peptide, whereas synthesis of the latter results in vesicle growth.
The creation of synthetic living cellular systems is usually approached from two different directions. In the top-down method, the genome of a bacterium is reduced to its essential components, ultimately leading to a minimal cell. In the bottom-up approach, artificial cells are assembled de novo from molecular components or cellular subsystems, which need to be functionally integrated into a consistent cell-like system.
In the de novo approach, compartmentalization of the necessary biochemical components is usually achieved using membranes made from phospholipids or fatty acids1,2
1. Expression of Elastin-like Polypeptides
Vesicle production
Figure 1 shows transmission electron microscopy (TEM) images of vesicles prepared with different swelling solutions and the glass beads method (also see Vogele et al.11). For the sample in Figure 1A, only PBS was used as swelling solution to prove the formation of vesicles and to determine their size. When TX-TL was used as swelling solution (Figure 1B), the vesicles .......
Film rehydration is a common procedure for the creation of small unilamellar vesicles. The main source of failure is the wrong handling of the materials used in the procedure.
Initially, the ELPs are produced by E. coli cells. The yield after ELP purification can vary significantly depending on how carefully the protocol is conducted during its crucial steps. These are the inverse temperature cycling (ITC) step and th.......
We gratefully acknowledge financial support through the DFG TRR 235 (Emergence of Life, project P15), the European Research Council (grant agreement no. 694410 AEDNA), and the TUM International Graduate School for Science and Engineering IGSSE (project no. 9.05). We thank E. Falgenhauer for her help with sample preparation. We thank A. Dupin and M. Schwarz-Schilling for their help with the TX-TL system and useful discussions. We thank N. B. Holland for useful discussions.
....Name | Company | Catalog Number | Comments |
2xYT | MP biomedicals | 3012-032 | |
3-PGA | Sigma-Aldrich | P8877 | |
5PRIME Phase Lock GelTM tube | VWR | 733-2478 | |
alkine-conjugated Cy3 | Sigma-Aldrich | 777331 | |
alkine-conjugated Cy5 | Sigma-Aldrich | 777358 | |
ATP | Sigma-Aldrich | A8937 | |
benzamidin | Carl Roth | CN38.2 | |
BL21 Rosetta 2 E. coli strain | Novagen | 71402 | |
Bradford BSA Protein Assay Kit | Bio-rad | 500-0201 | |
cAMP | Sigma-Aldrich | A9501 | |
carbenicillin | Carl Roth | 6344.2 | |
Chloramphenicol | Sigma-Aldrich | C1919 | |
chloramphenicol | Carl Roth | 3886.3 | |
chloroform | Carl Roth | 4432.1 | |
CoA | Sigma-Aldrich | C4282 | |
CTP | USB | 14121 | |
CuSO4 | Carl Roth | P024.1 | |
DFHBI | Lucerna Technologies | 410 | |
DMSO | Carl Roth | A994.1 | |
DNase I | NEB | M0303S | |
DTT | Sigma-Aldrich | D0632 | |
Ethanol | Carl Roth | 9065.2 | |
Folinic acid | Sigma-Aldrich | F7878 | |
Glass beads, acid-washed | Sigma-Aldrich | G1277 | |
GTP | USB | 16800 | |
HEPES | Sigma-Aldrich | H6147 | |
IPTG (β-isopropyl thiogalactoside ) | Sigma-Aldrich | I6758 | |
KCl | Carl Roth | P017.1 | |
K-glutamate | Sigma-Aldrich | G1149 | |
LB Broth | Carl Roth | X968.2 | |
lysozyme | Sigma-Aldrich | L6876 | |
methanol | Carl Roth | 82.2 | |
MgCl2 | Carl Roth | KK36.3 | |
Mg-glutamate | Sigma-Aldrich | 49605 | |
Micro Bio-Spin Chromatography Columns | Bio-Rad | 732-6204 | |
NAD | Sigma-Aldrich | N6522 | |
NHS-azide linker (y-azidobutyric acid oxysuccinimide ester) | Baseclick | BCL-033-5 | |
PEG-8000 | Carl Roth | 263.2 | |
pH stripes | Carl Roth | 549.2 | |
phenylmethylsulfonyl fluoride | Carl Roth | 6367.2 | |
phosphate-buffered saline | VWR | 76180-684 | |
phosphoric acid | Sigma-Aldrich | W290017 | |
polyethyleneimine | Sigma-Aldrich | 408727 | |
Potassium phosphate dibasic solution | Sigma-Aldrich | P8584 | |
Potassium phosphate monobasic solution | Sigma-Aldrich | P8709 | |
Qiagen Miniprep Kit | Qiagen | 27106 | |
RNAPol reaction buffer | NEB | B9012 | |
RNase inhibitor murine | NEB | M0314S | |
RNaseZap Wipes | ThermoFisher | AM9788 | |
rNTP | NEB | N0466S | |
Roti-Phenol/Chloroform/Isoamyl alcohol | Carlroth | A156.1 | |
RTS Amino Acid Sampler | 5 Prime | 2401530 | |
Slide-A-Lyzer Dialysis Cassettes, 10k MWCO (Kit) | Thermo-Scientific | 66382 | |
sodium chloride | Carl Roth | 9265.1 | |
sodium hydroxide | Carl Roth | 8655.1 | |
Spermidine | Sigma-Aldrich | 85558 | |
sterile-filtered (0.22 µm filter) | Carl Roth | XH76.1 | |
T7 polymerase | NEB | M0251S | |
TBTA (tris(benzyltriazolylmethyl)amine) | Sigma-Aldrich | 678937 | |
TCEP (tris(2-carboxyethyl)-phosphine hydrochloride) | Sigma-Aldrich | C4706 | |
Tris base | Fischer | BP1521 | |
tRNA (from E. coli) | Roche Applied Science | MRE600 | |
UTP | USB | 23160 |
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