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* These authors contributed equally
This protocol describes the inverted emulsion method used to encapsulate a cell-free expression (CFE) system within a giant unilamellar vesicle (GUV) for the investigation of the synthesis and incorporation of a model membrane protein into the lipid bilayer.
Cell-free expression (CFE) systems are powerful tools in synthetic biology that allow biomimicry of cellular functions like biosensing and energy regeneration in synthetic cells. Reconstruction of a wide range of cellular processes, however, requires successful reconstitution of membrane proteins into the membrane of synthetic cells. While the expression of soluble proteins is usually successful in common CFE systems, the reconstitution of membrane proteins in lipid bilayers of synthetic cells has proven to be challenging. Here, a method for reconstitution of a model membrane protein, bacterial glutamate receptor (GluR0), in giant unilamellar vesicles (GUVs) as model synthetic cells based on encapsulation and incubation of the CFE reaction inside synthetic cells is demonstrated. Utilizing this platform, the effect of substituting the N-terminal signal peptide of GluR0 with proteorhodopsin signal peptide on successful cotranslational translocation of GluR0 into membranes of hybrid GUVs is demonstrated. This method provides a robust procedure that will allow cell-free reconstitution of various membrane proteins in synthetic cells.
Bottom-up synthetic biology has gained increasing interest over the past decade as an emerging field with numerous potential applications in bioengineering, drug delivery, and regenerative medicine1,2. The development of synthetic cells as a cornerstone of bottom-up synthetic biology, in particular, has attracted a wide range of scientific communities due to the promising applications of synthetic cells as well as their cell-like physical and biochemical properties that facilitate in vitro biophysical studies3,4,5<....
The reagents and equipment utilized for this study are provided in the Table of Materials.
1. Bulk CFE reactions in the presence of small unilamellar vesicles (SUVs)
Prior to encapsulation of the CFE reactions, two variants of GluR0-sfGFP harboring native and proteorhodopsin signal peptides (signal peptide sequences are presented in Supplementary Table 1), and the soluble sfGFP were individually expressed in bulk reactions, and their expression was monitored by detecting the sfGFP signal using a plate reader (Figure 2A). Membrane proteins were expressed in the absence or presence of 100 nm SUVs. Additionally, using .......
Virtually any cellular process that depends on the transfer of molecules or information across the cell membrane, like cell signaling or cell excitation, requires membrane proteins. Thus, the reconstitution of membrane proteins has become the main bottleneck in realizing various synthetic cell designs for different applications. Traditional detergent-mediated reconstitution of membrane proteins in biological membranes requires GUV generation methods such as gentle swelling or electroformation. Swelling approaches usually.......
APL acknowledges support from the National Science Foundation (EF1935265), the National Institutes of Health (R01-EB030031 and R21-AR080363), and the Army Research Office (80523-BB)
....Name | Company | Catalog Number | Comments |
100 nm polycarbonate filter | STERLITECH | 1270193 | |
96 Well Clear Bottom Plate | ThermoFisher Scientific | 165305 | |
BioTek Synergy H1M Hybrid Multi-Mode Reader | Agilent | 11-120-533 | |
Creatine phosphate | Millipore Sigma | 10621714001 | |
CSU-X1 Confocal Scanner Unit | Yokogawa | CSU-X1Â | |
Density gradient medium (Optiprep) | Millipore Sigma | D1556 | Optional to switch with sucrose in inner solution |
Filter supports | Avanti | 610014 | |
Fisherbrand microtubes (1.5 mL) | Fisher Scientific | 05-408-129Â | |
Folinic acid calcium salt hydrate | Millipore Sigma | F7878 | |
Glucose | Millipore Sigma | 158968 | |
HEPES | Millipore Sigma | H3375 | |
iXon X3 camera | Andor | DU-897E-CS0 | |
L-Glutamic acid potassium salt monohydrate | Millipore Sigma | G1501 | |
Light mineral oil | Millipore Sigma | M5904 | |
Magnesium acetate tetrahydrate | Millipore Sigma | M5661 | |
Mini-extruder kit (including syringe holder and extruder stand) | Avanti | 610020 | |
Olympus IX81 Inverted Microscope | Olympus | IX21 | |
Olympus PlanApo N 60x Oil Microscope Objective | Olympus | 1-U2B933 | |
PEO-b-PBD | Polymer Source | P41745-BdEO | |
pET28b-PRSP-GluR0-sfGFP plasmid DNA | Homemade | N/A | |
pET28b-sfGFP-sfCherry(1-10) plasmid DNA | Homemade | N/A | |
pET28b-WT-GluR0-sfGFP plasmid DNA | Homemade | N/A | |
POPC lipid in chloroform | Avanti | 850457C | |
Potassium chloride | Millipore Sigma | P9541 | |
PUREfrex 2.0 | Cosmo Bio USA | GFK-PF201 | |
Ribonucleotide Solution Set | New England BioLabs | N0450 | |
RNase Inhibitor, Murine | New England BioLabs | M0314S | |
RTS Amino Acid Sampler | Biotechrabbit | BR1401801 | |
Sodium chloride | Millipore Sigma | S9888 | |
Spermidine | Millipore Sigma | S2626 | |
Sucrose | Millipore Sigma | S0389 | |
VAPRO Vapor Pressure Osmometer Model 5600 | ELITechGroup | VAPRO 5600 |
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