Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

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.

Abstract

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.

Introduction

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

Protocol

1. Expression of Elastin-like Polypeptides

  1. Day 1: Preparation of a starter culture and supplies for peptide expression
    1. Prepare and autoclave expression culture flasks (4 x 2.5 L) and 3 L of LB medium. For 1 L of LB medium, add 25 g of LB powder to 1 L of ultrapure water.
    2. Prepare a starter culture with 100 mL of LB medium, 50 µL of sterile-filtered (0.22 µm filter) chloramphenicol solution (25 mg/mL in EtOH), and 50 µL of sterile-filtered (0.22 µm fil.......

Representative Results

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 .......

Discussion

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.......

Acknowledgements

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.

....

Materials

NameCompanyCatalog NumberComments
2xYTMP biomedicals3012-032
3-PGASigma-AldrichP8877
5PRIME Phase Lock GelTM tubeVWR733-2478
alkine-conjugated Cy3Sigma-Aldrich777331
alkine-conjugated Cy5Sigma-Aldrich777358
ATPSigma-AldrichA8937
benzamidinCarl RothCN38.2
BL21 Rosetta 2 E. coli strainNovagen71402
Bradford BSA Protein Assay KitBio-rad500-0201
cAMPSigma-AldrichA9501
carbenicillinCarl Roth6344.2
ChloramphenicolSigma-AldrichC1919
chloramphenicolCarl Roth3886.3
chloroformCarl Roth4432.1
CoASigma-AldrichC4282
CTPUSB14121
CuSO4Carl RothP024.1
DFHBILucerna Technologies410
DMSOCarl RothA994.1
DNase INEBM0303S
DTTSigma-AldrichD0632
EthanolCarl Roth9065.2
Folinic acidSigma-AldrichF7878
Glass beads, acid-washedSigma-AldrichG1277
GTPUSB16800
HEPESSigma-AldrichH6147
IPTG (β-isopropyl thiogalactoside )Sigma-AldrichI6758
KClCarl RothP017.1
K-glutamateSigma-AldrichG1149
LB BrothCarl RothX968.2
lysozymeSigma-AldrichL6876
methanolCarl Roth82.2
MgCl2Carl RothKK36.3
Mg-glutamateSigma-Aldrich49605
Micro Bio-Spin Chromatography ColumnsBio-Rad732-6204
NADSigma-AldrichN6522
NHS-azide linker (y-azidobutyric acid oxysuccinimide ester)BaseclickBCL-033-5
PEG-8000Carl Roth263.2
pH stripesCarl Roth549.2
phenylmethylsulfonyl fluorideCarl Roth6367.2
phosphate-buffered salineVWR76180-684
phosphoric acidSigma-AldrichW290017
polyethyleneimineSigma-Aldrich408727
Potassium phosphate dibasic solutionSigma-AldrichP8584
Potassium phosphate monobasic solutionSigma-AldrichP8709
Qiagen Miniprep KitQiagen27106
RNAPol reaction bufferNEBB9012
RNase inhibitor murineNEBM0314S
RNaseZap WipesThermoFisherAM9788
rNTPNEBN0466S
Roti-Phenol/Chloroform/Isoamyl alcoholCarlrothA156.1
RTS Amino Acid Sampler5 Prime2401530
Slide-A-Lyzer Dialysis Cassettes, 10k MWCO (Kit)Thermo-Scientific66382
sodium chlorideCarl Roth9265.1
sodium hydroxideCarl Roth8655.1
SpermidineSigma-Aldrich85558
sterile-filtered (0.22 µm filter)Carl RothXH76.1
T7 polymeraseNEBM0251S
TBTA (tris(benzyltriazolylmethyl)amine)Sigma-Aldrich678937
TCEP (tris(2-carboxyethyl)-phosphine hydrochloride)Sigma-AldrichC4706
Tris baseFischerBP1521
tRNA (from E. coli)Roche Applied ScienceMRE600
UTPUSB23160

References

  1. Chen, I. A., Szostak, J. W. A kinetic study of the growth of fatty acid vesicles. Biophysical Journal. 87 (2), 988-998 (2004).
  2. Nourian, Z., Roelofsen, W., Danelon, C. Triggered gene expression in fed-vesicle micro....

Explore More Articles

Peptide Membrane PrecursorsAutonomous Vesicle GrowthFilm Re hydrationReaction CompartmentsELP SolutionChloroform MethanolGlass BeadsRotary EvaporatorVesicle FormationPlasmid DNA PurificationPhase SeparationEthanol Precipitation

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved