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Structural and biochemical studies of human membrane transporters require milligram quantities of stable, intact, and homogeneous protein. Here we describe scalable methods to screen, express, and purify human solute carrier transporters using codon-optimized genes.
Solute carriers (SLCs) are membrane transporters that import and export a range of endogenous and exogenous substrates, including ions, nutrients, metabolites, neurotransmitters, and pharmaceuticals. Despite having emerged as attractive therapeutic targets and markers of disease, this group of proteins is still relatively underdrugged by current pharmaceuticals. Drug discovery projects for these transporters are impeded by limited structural, functional, and physiological knowledge, ultimately due to the difficulties in the expression and purification of this class of membrane-embedded proteins. Here, we demonstrate methods to obtain high-purity, milligram quantities of human SLC transporter proteins using codon-optimized gene sequences. In conjunction with a systematic exploration of construct design and high-throughput expression, these protocols ensure the preservation of the structural integrity and biochemical activity of the target proteins. We also highlight critical steps in the eukaryotic cell expression, affinity purification, and size-exclusion chromatography of these proteins. Ultimately, this workflow yields pure, functionally active, and stable protein preparations suitable for high-resolution structure determination, transport studies, small-molecule engagement assays, and high-throughput in vitro screening.
Membrane proteins have long been targets for researchers and pharmaceutical industries alike. Of these, the solute carriers (SLCs) are a family of over 400 secondary transporter genes encoded within the human genome1. These transporters are involved in the import and export of numerous molecules, including ions2, neurotransmitters3, lipids4,5,6,7, amino acids8, nutrients9,10,
NOTE: All codon-optimized RESOLUTE SLC genes have been deposited into AddGene43, the links to which are available on the list of RESOLUTE public reagents44. These genes have been cloned into the pDONR221 plasmid and allow direct cloning of the genes into the destination vector using recombination cloning45. To maximize parallelism, bacterial, insect, and mammalian cells are grown in block format for bacmid production (section 3), baculovirus amplification (section 5), and expression testing (section 6), respectively. For these steps, a micro-expression shaker is required to ensure sufficient ....
SLC genes can be cloned from RESOLUTE pDONR plasmids into BacMam vectors for mammalian expression
The described protocols for cloning, expression, and purification have proven successful for many SLC transporters across multiple protein folds. Nevertheless, the procedures include several checkpoints for monitoring progress, allowing for optimization to account for differences in expression, protein folding, lipid- and detergent-dependent stability, and sensitivity to buffer conditions.
The development of SLC-targeting therapies has remained hampered due to the absence of systematic characterization of transporter function. This has led to disproportionally fewer drugs targeting this protein class relative to GPCRs and ion channels63, despite their numerous roles in normal and pathophysiological processes. RESOLUTE is an international consortium aimed at developing cutting-edge research techniques and tools to accelerate and improve current SLC research. As a part of RESOLUTE, we.......
The authors declare no competing financial interests.
This work was performed within the RESOLUTE project. RESOLUTE has received funding from the Innovative Medicines Initiative 2 Joint Undertaking under grant agreement No 777372. This Joint Undertaking receives support from the European Union's Horizon 2020 research and innovation programme and EFPIA. This article reflects only the authors' views and neither IMI nor the European Union and EFPIA are responsible for any use that may be made of the information contained therein. The pHTBV plasmid was kindly provided by Prof. Frederick Boyce (Harvard).
....Name | Company | Catalog Number | Comments |
3C protease | Produced in-house | ||
50 or 100 kDa cut-off centrifugal concentrators | Sartorius | VS0242 | |
5-Cyclohexyl-1-Pentyl-β-D-Maltoside | Anatrace | C325 | CYMAL-5 |
96-well bacmid purification kit | Millipore | LSKP09604 | Montage Plasmid Miniprep |
96-well block (2 mL) | Greiner Bio-One | 780271 | |
Adhesive plastic seals | Qiagen | 19570 | Tape Pads |
Agarose size exclusion chromatography column | Cytiva | 29091596 | Superose 6 Increase 10/300 GL |
Benzonase DNAse | Produced in-house | ||
BisTris | Sigma Aldrich | B9754 | |
Cholesteryl Hemisuccinate Tris salt | Anatrace | CH210 | CHS |
Cobalt metal affinity resin | Takara Bio | 635653 | TALON Metal Affinity Resin |
D(+)-Biotin | Sigma Aldrich | 851209 | |
Dextran-agarose size exclusion chromatography column | Cytiva | 28990944 | Superdex 200 Increase 10/300 GL |
Digitonin | Apollo Scientific | BID3301 | |
Dounce tissue grinder (40 mL) | DWK Life Sciences | 357546 | |
EDTA-free protease inhibitor cocktail | Sigma Aldrich | 4693132001 | cOmplete, EDTA-free Protease Inhibitor Cocktail |
Fetal Bovine Serum | Thermo Fisher | 10500064 | |
Fos-Choline-12 | Anatrace | F308S | FS-12 |
Glycerol | Sigma Aldrich | G5516 | |
Glyco-diosgenin | Anatrace | GDN101 | GDN |
Gravity flow columns | Cole-Parmer | WZ-06479-25 | |
HEK293 medium | Thermo Fisher | 12338018 | FreeStyle 293 medium |
HEPES | Apollo Scientific | BI8181 | |
Hydrophilic, neutral silica UHPLC column | Sepax | 231300-4615 | Unix-C SEC-300 4.6 x 150 |
Imidazole | Sigma Aldrich | 56750 | |
Insect transfection reagent | Sigma Aldrich | 71259 | Reagent |
Lauryl Maltose Neopentyl Glycol | Anatrace | NG310 | LMNG |
Magnesium Chloride Hexahydrate | Sigma Aldrich | M2670 | |
Micro-expression shaker | Glas-Col | 107A DPMINC24CE | |
NaCl | Sigma Aldrich | S9888 | |
n-Decyl-β-D-Maltoside | Anatrace | D322 | DM |
n-Dodecyl-b-D-Maltopyranoside | Anatrace | D310 | DDM |
n-Dodecyl-N,N-Dimethylamine-N-Oxide | Anatrace | D360 | LDAO |
n-Nonyl-β-D-Glucopyranoside | Anatrace | N324S | NG |
n-Octyl-d17-β-D-Glucopyranoside | Anatrace | O311D | OGNG |
Octaethylene Glycol Monododecyl Ether | Anatrace | O330 | C12E8 |
Octyl Glucose Neopentyl Glycol | Anatrace | NG311 | OGNG |
Phosphate Buffered Saline | Sigma Aldrich | D8537 | DPBS |
Polyoxyethylene(10)dodecyl Ether | Anatrace | AP1210 | C12E10 |
Polyoxyethylene(9)dodecyl Ether | Anatrace | APO129 | C12E9 |
Porous seal for tissue culture plates | VWR | 60941-084 | Rayon Films for Biological Cultures |
Proteinase K | New England Biolabs | P8107S | |
Recombination enzyme mix | Thermo Fisher | 11791020 | Gateway LR Clonase II |
Serum-free insect media | Gibco | 10902088 | Sf-900 II serum-free media |
Sodium Butyrate | Sigma Aldrich | 303410 | |
Sonicator 24-head probe | Sonics | 630-0579 | |
Sonicator power unit | Sonics | VCX 750 | |
Strep-Tactin resin | IBA Life Sciences | 2-5030-025 | Strep-TactinXT 4Flow high- capacity resin |
Sucrose | Sigma Aldrich | S7903 | |
Sucrose Monododecanoate | Anatrace | S350 | DDS |
Suspension-adapted HEK293 cells | Thermo Fisher | A14527 | Expi293F |
Transfection reagent | Sigma Aldrich | 70967 | GeneJuice Transfection Reagent |
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