Name: small-scale plasma membrane preparation for the analysis of candida albicans cdr1-mgfphis
Uploaded: 2021-06-13T15:00:00
Description: Watch this Scientific Journal Video about Small-Scale Plasma Membrane Preparation for the Analysis of Candida albicans Cdr1-mGFPHis at JoVE.com

The authors gratefully acknowledge funding from the New Zealand Marsden Fund (Grant UOO1305), and a block grant from Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand (M. Niimi). They wish to thank the University of Otago for providing G. Madani with a PhD Scholarship. The authors also wish to express their gratitude to Professor Stefan Raunser and his colleagues, Dr Amir Apelbaum, and Dr Deivanayagabarathy Vinayagam, for their support and supervision during a 6-month visit of G. Madani at the Max Planck Institute of Molecular Physiology (MPIMP), Dortmund, Germany. The authors also thank the German Academic Exchange Service (DAAD) for providing G. Madani with a research grant (57381332) to visit the MPIMP.

1. Preparation of fresh or frozen stocks of transformation competent AD&#916; and AD&#916;&#916; cells
<ol>
	<li>Inoculate 25 mL of 2x YPCD [i.e., 2x YPD; 2% (w/v) yeast extract, 2% (w/v) peptone, 4% (w/v) dextrose), 0.079 % (w/v) CSM (complete supplement mixture)]35 medium with a single yeast colony and incubate overnight (o/n) for 16 h at 30 &#176;C with shaking at 200 revolutions per minute (rpm).</li>
	<li>Inoculate 225 mL of 2x YPCD medium with the 25 mL&#160;o/n culture and check the cell ...

Despite recent progress in the structural analysis of membrane proteins, no 3D structure for Cdr1, or any other PDR transporter, is currently available. So, gaining knowledge of the Cdr1 structure and its biochemical features is important, as this will not only provide insight into rational design of novel drugs to overcome efflux-mediated drug resistance, but also into the mechanism of function of an important subfamily of ABC proteins.
One of the main requirements for the structural characte...

The extraction of integral membrane proteins from their native lipid environment can dramatically affect their structure and function1,2,3,4. The complex lipid composition of biological membranes5 ensures that critically important protein-lipid interactions can occur6. Lipids maintain the structural integrity of membrane proteins, thus enabling them to function correctly in their membrane compartment destination(s)7,8. Therefore, a critical first step in the membrane protein purification is the extraction of the protein from its native environment without affecting its structure and/or function.
There are many obstacles to characterizing the structure of membrane proteins, most of which are related to their hydrophobic nature, and the difficulties of expressing properly folded and functional membrane proteins in the quantities required for X-ray crystallography or cryo-electron microscopy (cryo-EM)9,10,11,12. There are three types of membrane protein expression systems: homologous9, heterologous13,14,15, and in vitro expression systems16,17. The often-low expression levels, or the prohibitive costs, of many expression systems leave only a few hosts as the preferred option to produce membrane proteins. They include the bacterial host, Escherichia coli, the yeasts S. cerevisiae and Pichia pastoris, and higher eukaryotes such as Sf9 insect cells or mammalian cell lines18. All membrane protein expression technologies have advantages and disadvantages; however, S. cerevisiae is perhaps the best studied eukaryotic model organism suitable for membrane protein production. It is highly versatile with applications in genetic engineering, drug discovery, synthetic biology, and the expression of eukaryotic membrane proteins14,19,20,21.
In this study, a patented S. cerevisiae membrane protein expression technology21 was used, with S. cerevisiae AD&#916;14 and AD&#916;&#916;22 as the preferred hosts (Figure 1A), to overexpress and study the major C. albicans multidrug efflux pump Cdr1. Both the S. cerevisiae strains are derivatives of AD1-8u-&#160;23 that have either the ura3 (AD&#916;) or both the ura3 and his1 (AD&#916;&#916;) genes deleted to eliminate any false positive uracil or histidine prototroph transformants arising through the unwanted integration at the URA3 or the HIS1 genomic loci. The deletion of the 7 major multidrug efflux pumps23, indicated in Figure 1A, makes AD&#916;&#916; exquisitely sensitive to most xenobiotics. The gain-of-function mutant transcription factor Pdr1-3 causes the constitutive overexpression of heterologous membrane proteins such as Cdr1 (red octagons in Figure 1A) after integration of the heterologous-ORF-containing transformation cassette (Figure 1A) at the genomic PDR5 locus (blue rectangle in Figure 1A) via two homologous recombination events. Proper plasma membrane localization of C-terminally mGFPHis tagged proteins can be confirmed by confocal microscopy (Figure 1A), and the His tag can be used for nickel-affinity purification of the tagged protein. Cloning some fungal ABC transporters (e.g., Candida krusei ABC1) into pABC3-derived plasmids was, however, not possible because they could not be propagated&#160;in Escherichia coli due to cell toxicity. This prompted the development of the one-step cloning of membrane proteins14,24 tagged at either their N- or C-terminus with various affinity, epitope, or reporter tags directly into S. cerevisiae AD&#916;&#916; (Figure 1C). S. cerevisiae AD&#916;&#916; strains overexpressing various CDR1 mutants can also be created efficiently this way by using up to five individual PCR fragments that overlap by 25 bp (Figure 1C). Employing this protocol, many ORFs of interest can be cloned, expressed, and characterized at low cost and at high efficiency within a very short time span. The transformation efficiency reduces only ~2-fold with each additional PCR fragment.
If desired, expression levels can also be readily manipulated by primer design to predictably tune expression levels down to anywhere between 0.1%-50% of the usually high, constitutive expression levels25. The optimized, multifunctional, pABC314 derivative cloning vector, pABC3-XLmGFPHis26 (Figure 1B) contains a HRV-3C protease cleavage site (X; LEVLFQ|GP), a protease that performs better at 4 &#176;C than the frequently used tobacco etch virus (TEV) protease27. L is a five amino acid (GSGGS) linker, mGFP is a monomeric mutant (A206K)28,29 version of the yeast enhanced green-fluorescence protein variant yEGFP330, and His is a three amino acid linker (GGS) followed by the six-histidine (HHHHHH) nickel-affinity protein purification tag.
This expression technology has been successfully used in drug discovery and the study of membrane proteins. The first structure for a fungal azole drug target, S. cerevisiae Erg1131, was solved using this technology. It also enabled the detailed characterization of C. albicans Cdr132,33,34 and the creation of a cysteine-deficient Cdr1 molecule35 suitable for cysteine-crosslinking studies to verify any future high-resolution structure. Many other ABC transporters from major human fungal pathogens&#160;(i.e., C. albicans, Candida glabrata, Candida auris, Candida krusei, Candida utilis, Cryptococcus neoformans, Aspergillus fumigatus, Penicillium marneffei, and the Fusarium solani species complex) have also been studied in detail using this expression platform24,36,37,38,39. This has enabled the generation of a panel of S. cerevisiae strains overexpressing efflux pumps that has been used in high-throughput screens to discover the novel fluorescent efflux pump substrate Nile red40 and specific41 and broad-spectrum14,33,42,43,44&#160;efflux pump inhibitors. The use of this system also enabled the discovery of clorgyline as the first of its kind broad-spectrum fungal multidrug efflux pump inhibitor42.
Complete solubilization of membrane proteins and the creation of a homogeneous membrane protein-micelle preparation devoid of endogenous lipids, requires high detergent concentrations45. But unfortunately, this also often inactivates the membrane protein5,8,45,46. The properties of detergent monomers and their aggregation in solution are affected by the physical properties of the hydrophobic tail, the length and branching of the alkyl chain, the presence of an aromatic nucleus or fluoroalkyl side chain, or the number of polyoxyethylene units. Thus, detergent screening is an important first step to determine the most suitable detergent for membrane protein solubilization and purification.
C. albicans is a major human fungal pathogen of immunocompromised individuals that can cause serious, life threatening invasive infections47, and it can become resistant to azole antifungal drugs48,49. One of the main mechanisms of C. albicans multidrug resistance is the overexpression of Cdr150, which is a type II ATP-binding cassette (ABC) transporter51 of the ABCG subfamily located in the plasma membrane. Full-size fungal ABCG transporters (consisting of two nucleotide binding domains [NBDs] and two transmembrane domains [TMDs]) are more commonly known as pleiotropic drug resistance (PDR) transporters and are characterized by their unique inverted domain topology [NBD-TMD]2. PDR transporters are only found in plants52,53 and fungi54. Despite their importance, there are no structures for PDR transporters, although structures for human half-size ABCG transporters have recently been solved which helped create the first tentative model for Cdr133. Our recent experimental evidence suggests, however, that this model is flawed possibly because fungal PDR transporters have characteristic asymmetric NBDs resulting quite possibly in a unique transport mechanism. A high-resolution structure of Cdr1 is, therefore, required for both the rational design of novel efflux pump inhibitors that may help overcome efflux-mediated drug resistance, and to provide insights into the mechanism of action of this important ABC transporter family.
The objective of this study was to develop reliable protocols for the expression, solubilization, and purification of Cdr1 in the genetically modified S. cerevisiae expression host, with the ultimate aim of obtaining a high-resolution structure for Cdr1. As part of this process, a protease-cleavable mGFPHis double tag (Figure 1B) was designed with a 16-residue linker separating the tag from the C-terminus of Cdr1, which improved binding of the attached 6x His affinity tag to the nickel-affinity resin and enabled the monitoring of Cdr1 expression levels in living cells and during the entire purification process. A reproducible protocol for small-scale yeast plasma membrane protein preparations containing about 10% C. albicans Cdr1 (as estimated by Coomassie staining after SDS-PAGE) was also developed, which could be used for the biochemical characterization of Cdr1.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>2-(N-Morpholino)ethane-sulphonic acid (MES)</td>
			<td>Sigma-Aldrich</td>
			<td>M3671</td>
			<td></td>
		</tr>
		<tr>
			<td>2-Amino-2-(hydroxymethyl)-1,3-propanediol (Tris base; ultra-pure)</td>
			<td>Merck</td>
			<td>77-86-1</td>
			<td></td>
		</tr>
		<tr>
			<td>2,2-Didecylpropane-1,3-bis-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>NG310S</td>
			<td>LMNG</td>
		</tr>
		<tr>
			<td>2,2-Dihexylpropane-1,3-bis-&#946;-D-glucopyranoside</td>
			<td>Anatrace</td>
			<td>NG311S</td>
			<td>OGNG (MNG-OG)</td>
		</tr>
		<tr>
			<td>2,2-Dioctylpropane-1,3-bis-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>NG322S</td>
			<td>DMNG</td>
		</tr>
		<tr>
			<td>4-Trans-(4-trans-propylcyclohexyl)-cyclohexyl &#945;-D-maltopyranoside</td>
			<td>Glycon Biochemicals GmbH</td>
			<td>D99019-C</td>
			<td>PCC-&#945;-M</td>
		</tr>
		<tr>
			<td>40% Acrylamide/Bis-acrylamide (37.5:1)</td>
			<td>Bio-Rad</td>
			<td>1610148</td>
			<td></td>
		</tr>
		<tr>
			<td>Acetic acid (glacial)</td>
			<td>Merck</td>
			<td>64-19-7</td>
			<td></td>
		</tr>
		<tr>
			<td>Agar</td>
			<td>Formedium</td>
			<td>&#160;009002-18-0</td>
			<td></td>
		</tr>
		<tr>
			<td>Ammonium molybdate</td>
			<td>Sigma-Aldrich</td>
			<td>13106-76-8</td>
			<td></td>
		</tr>
		<tr>
			<td>Ammonium persulphate (APS)</td>
			<td>Bio-Rad</td>
			<td>1610700</td>
			<td></td>
		</tr>
		<tr>
			<td>ATP disodium salt</td>
			<td>sigma-Aldrich</td>
			<td>A-6419</td>
			<td></td>
		</tr>
		<tr>
			<td>Bromophenol blue</td>
			<td>SERVA Electrophoresis GmbH</td>
			<td>34725-61-6</td>
			<td></td>
		</tr>
		<tr>
			<td>CHAPS</td>
			<td>Anatrace</td>
			<td>C316S</td>
			<td></td>
		</tr>
		<tr>
			<td>CHAPSO</td>
			<td>Anatrace</td>
			<td>C317S</td>
			<td></td>
		</tr>
		<tr>
			<td>CSM</td>
			<td>Formedium</td>
			<td>DCS0019</td>
			<td></td>
		</tr>
		<tr>
			<td>CSM minus uracil</td>
			<td>Formedium</td>
			<td>DCS0161</td>
			<td></td>
		</tr>
		<tr>
			<td>Cyclohexyl-1-butyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>C324S</td>
			<td>CYMAL-4</td>
		</tr>
		<tr>
			<td>Cyclohexyl-1-heptyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>C327S</td>
			<td>CYMAL-7</td>
		</tr>
		<tr>
			<td>Cyclohexyl-methyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>C321S</td>
			<td>CYMAL-1</td>
		</tr>
		<tr>
			<td>Digitonin</td>
			<td>Sigma-Aldrich</td>
			<td>11024-24-1</td>
			<td></td>
		</tr>
		<tr>
			<td>Dithiothreitol (DTT)</td>
			<td>Roche Diagnostics</td>
			<td>10197785103</td>
			<td></td>
		</tr>
		<tr>
			<td>DMSO</td>
			<td>Merck</td>
			<td>67-68-5</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethanol</td>
			<td>Merck</td>
			<td>459836</td>
			<td></td>
		</tr>
		<tr>
			<td>Ethylenediaminetetraacetic acid disodium salt (EDTA; Titriplex III)</td>
			<td>Merck</td>
			<td>6381-92-6</td>
			<td></td>
		</tr>
		<tr>
			<td>ExoSAP-IT PCR Product Cleanup Reagent</td>
			<td>Applied Biosystems</td>
			<td>78205</td>
			<td>A blend of exonuclease and phosphatase</td>
		</tr>
		<tr>
			<td>Glucose</td>
			<td>Formedium</td>
			<td>50-99-7</td>
			<td></td>
		</tr>
		<tr>
			<td>Glycerol</td>
			<td>Merck</td>
			<td>56-81-5</td>
			<td></td>
		</tr>
		<tr>
			<td>Glycine</td>
			<td>Merck</td>
			<td>G8898</td>
			<td></td>
		</tr>
		<tr>
			<td>HEPES</td>
			<td>Formedium</td>
			<td>7365-45-9</td>
			<td></td>
		</tr>
		<tr>
			<td>Hydrochloric acid</td>
			<td>Merck</td>
			<td>1003172510</td>
			<td></td>
		</tr>
		<tr>
			<td>KOD Fx Neo</td>
			<td>TOYOBO Co</td>
			<td>KFX-201</td>
			<td>Use for reliable colony PCR</td>
		</tr>
		<tr>
			<td>lithium acetate (LiAc)</td>
			<td>Sigma-Aldrich</td>
			<td>546-89-4</td>
			<td></td>
		</tr>
		<tr>
			<td>Magnesium chloride hexa-hydrate</td>
			<td>sigma-Aldrich</td>
			<td>M2393</td>
			<td></td>
		</tr>
		<tr>
			<td>MES</td>
			<td>Formedium</td>
			<td>145224-94-8</td>
			<td></td>
		</tr>
		<tr>
			<td>n-Decanoyl-N-hydroxyethyl-glucamide</td>
			<td>Anatrace</td>
			<td>H110S</td>
			<td>HEGA-10</td>
		</tr>
		<tr>
			<td>n-Decanoyl-N-methyl-glucamide</td>
			<td>Anatrace</td>
			<td>M320S</td>
			<td>MEGA-10</td>
		</tr>
		<tr>
			<td>n-Decyl-phosphocholine</td>
			<td>Anatrace</td>
			<td>F304S</td>
			<td>Fos-choline-10</td>
		</tr>
		<tr>
			<td>n-Decyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>D322S</td>
			<td>DM</td>
		</tr>
		<tr>
			<td>n-Dodecyl-N,N-dimethyl-3-ammonio-1-propanesulphonate</td>
			<td>Anatrace</td>
			<td>AZ312S</td>
			<td>Anzergent 3-12</td>
		</tr>
		<tr>
			<td>n-Dodecyl-N,N-dimethylamine-N-oxide</td>
			<td>Anatrace</td>
			<td>D360S</td>
			<td>LDAO</td>
		</tr>
		<tr>
			<td>n-Dodecyl-&#945;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>D310HA</td>
			<td>&#945;-DDM</td>
		</tr>
		<tr>
			<td>n-Dodecyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>D310S</td>
			<td>&#946;-DDM</td>
		</tr>
		<tr>
			<td>n-Nonyl-&#946;-D-glucopyranoside</td>
			<td>Anatrace</td>
			<td>N324S</td>
			<td>NG</td>
		</tr>
		<tr>
			<td>n-Nonyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>N330S</td>
			<td>NM</td>
		</tr>
		<tr>
			<td>n-Octadecyl-N,N-dimethyl-3-ammonio-1-propanesulphonate</td>
			<td>Anatrace</td>
			<td>AZ318S</td>
			<td>Anzergent 3-18</td>
		</tr>
		<tr>
			<td>n-Octyl-N,N-dimethyl-3-ammonio-1-propanesulphonate</td>
			<td>Anatrace</td>
			<td>AZ308S</td>
			<td>Anzergent 3-8</td>
		</tr>
		<tr>
			<td>n-Octyl-phosphocholine</td>
			<td>Anatrace</td>
			<td>F300S</td>
			<td>Fos-choline-8</td>
		</tr>
		<tr>
			<td>n-Octyl-&#946;-D-glucopyranoside</td>
			<td>Anatrace</td>
			<td>O311S</td>
			<td>OG</td>
		</tr>
		<tr>
			<td>n-Tetradecyl-phosphocholine</td>
			<td>Anatrace</td>
			<td>F312S</td>
			<td>Fos-choline-14</td>
		</tr>
		<tr>
			<td>n-Tetradecyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>T315S</td>
			<td>TDM</td>
		</tr>
		<tr>
			<td>n-Tridecyl-phosphocholine</td>
			<td>Anatrace</td>
			<td>F310S</td>
			<td>Fos-choline-13</td>
		</tr>
		<tr>
			<td>n-Tridecyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>T323S</td>
			<td>-</td>
		</tr>
		<tr>
			<td>n-Undecyl-&#946;-D-maltopyranoside</td>
			<td>Anatrace</td>
			<td>U300S</td>
			<td>UM (UDM)</td>
		</tr>
		<tr>
			<td>N,N,N&#8217;,N&#8217;-tetramethyl-ethylenediamine (TEMED)</td>
			<td>Sigma-Aldrich</td>
			<td>T9281</td>
			<td></td>
		</tr>
		<tr>
			<td>Octylphenoxypolyethoxyethanol</td>
			<td>Sigma-Aldrich</td>
			<td>9002-93-1</td>
			<td>TRITON X-100</td>
		</tr>
		<tr>
			<td>Oligomycin</td>
			<td>Sigma-Aldrich</td>
			<td>75351</td>
			<td></td>
		</tr>
		<tr>
			<td>Peptone</td>
			<td>Formedium</td>
			<td>3049-73-7</td>
			<td></td>
		</tr>
		<tr>
			<td>phenylmethylsulfonyl fluoride (PMSF)</td>
			<td>Roche Diagnostics</td>
			<td>329-98-6</td>
			<td></td>
		</tr>
		<tr>
			<td>Phusion&#160;Hot Start Flex DNA Polymerase</td>
			<td>New England Biolabs</td>
			<td>M0535S</td>
			<td>High-fidelity DNA polymerase</td>
		</tr>
		<tr>
			<td>polyethylene glycol (PEG 3350)</td>
			<td>Sigma-Aldrich</td>
			<td>25322-68-3</td>
			<td></td>
		</tr>
		<tr>
			<td>polyoxyethylenesorbitan monooleate</td>
			<td>Sigma-Aldrich</td>
			<td>9005-65-6</td>
			<td>TWEEN 80</td>
		</tr>
		<tr>
			<td>Potassium nitrate</td>
			<td>Sigma-Aldrich</td>
			<td>P8394</td>
			<td></td>
		</tr>
		<tr>
			<td>Protein Assay Kit</td>
			<td>Bio-Rad</td>
			<td>5000122</td>
			<td>RC DC Protein Assay Kit II</td>
		</tr>
		<tr>
			<td>QC Colloidal Coomassie Stain</td>
			<td>Bio-Rad</td>
			<td>1610803</td>
			<td></td>
		</tr>
		<tr>
			<td>Prism Ultra Protein Ladder (10-245 kDa)</td>
			<td>Abcam</td>
			<td>AB116028</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium azide</td>
			<td>Sigma-Aldrich</td>
			<td>71289</td>
			<td></td>
		</tr>
		<tr>
			<td>Sodium dodecyl sulphate</td>
			<td>Sigma-Aldrich</td>
			<td>151-21-3</td>
			<td>SDS</td>
		</tr>
		<tr>
			<td>Sodium L-ascorbate BioXtra</td>
			<td>Sigma-Aldrich</td>
			<td>11140</td>
			<td></td>
		</tr>
		<tr>
			<td>Sucrose Monododecanoate</td>
			<td>Anatrace</td>
			<td>S350S</td>
			<td>DDS</td>
		</tr>
		<tr>
			<td>Sulphuric acid</td>
			<td>Sigma-Aldrich</td>
			<td>339741</td>
			<td></td>
		</tr>
		<tr>
			<td>Yeast extract</td>
			<td>Formedium</td>
			<td>008013-01-2</td>
			<td></td>
		</tr>
		<tr>
			<td>Yeast nitrogen base without amino acids</td>
			<td>Formedium</td>
			<td>CYN0402</td>
			<td></td>
		</tr>
		<tr>
			<td>&#160;Equipment (type)</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge&#160; (Eppendorf 5804)</td>
			<td>Eppendorf</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge (Beckman Ultra)</td>
			<td>Beckman</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge (Sorvall RC6)</td>
			<td>Sorvall</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>FSEC apparatus (NGC Chromatography Medium Pressure system equipped with a fluorescence detector, an autosampler, a fractionator)</td>
			<td>Bio-Rad</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Gel imaging (GelDoc EZ Imager)</td>
			<td>Bio-Rad</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Microplate reader (Synergy 2 Multi-Detection)</td>
			<td>BioTek Instruments</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>PCR thermal cycler (C1000 Touch)</td>
			<td>Bio-Rad</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Power supply (PowerPac)</td>
			<td>Bio-Rad</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>SDS PAGE (Mini-PROTEAN Tetra)</td>
			<td>Bio-Rad</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Shaking incubator (Multitron)</td>
			<td>Infors HT, Bottmingen</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Superose 6 Increase 10/300 GL</td>
			<td>GE Healthcare Life Sciences</td>
			<td>GE17-5172-01</td>
			<td></td>
		</tr>
		<tr>
			<td>UV/Visible spectrophotometer (Ultraspec 6300 pro)</td>
			<td colspan="2">Amersham BioSciences UK Ltd</td>
			<td></td>
		</tr>
	</tbody>
</table>

small-scale plasma membrane preparation for the analysis of candida albicans cdr1-mgfphis

The successful biochemical and biophysical characterization of ABC transporters depends heavily on the choice of the heterologous expression system. Over the past two decades, we have developed a yeast membrane protein expression platform that has been used to study many important fungal membrane proteins. The expression host Saccharomyces cerevisiae AD&#916;&#916; is deleted in seven major endogenous ABC transporters and it contains the transcription factor Pdr1-3 with a gain-of-function mutation that enables the constitutive overexpression of heterologous membrane protein genes stably integrated as single copies at the genomic PDR5 locus. The creation of versatile plasmid vectors and the optimization of one-step cloning strategies enables the rapid and accurate cloning, mutagenesis, and expression of heterologous ABC transporters. Here, we describe the development and use of a novel protease-cleavable mGFPHis double tag (i.e., the monomeric yeast enhanced green fluorescent protein yEGFP3 fused to a six-histidine affinity purification tag) that was designed to avoid possible interference of the tag with the protein of interest and to increase the binding efficiency of the His tag to nickel-affinity resins. The fusion of mGFPHis to the membrane protein ORF (open reading frame) enables easy quantification of the protein by inspection of polyacrylamide gels and detection of degradation products retaining the mGFPHis tag. We demonstrate how this feature facilitates detergent screening for membrane protein solubilization. A protocol for the efficient, fast, and reliable isolation of the small-scale plasma membrane preparations of the C-terminally tagged Candida albicans multidrug efflux transporter Cdr1 overexpressed in S. cerevisiae AD&#916;&#916;, is presented. This small-scale plasma membrane isolation protocol generates high-quality plasma membranes within a single working day. The plasma membrane preparations can be used to determine the enzyme activities of Cdr1 and Cdr1 mutant variants.

A high frequency of transformation of S. cerevisiae AD&#916;&#916; (~4 x 104 transformants/&#181;g) was achieved with pYES2 (Figure 2B). As expected, the no DNA (i.e., ddH2O only) control gave no transformants, and 1 &#181;g of the linear CDR1-mGFPHis transformation cassette (Figure 1A) gave ~50 transformants (Figure 2C)&#160;with the optimized AD&#916;&#916; transformation protocol. ...

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Small-Scale Plasma Membrane Preparation for the Analysis of Candida albicans Cdr1-mGFPHis

This article presents a small-scale plasma membrane isolation protocol for the characterization of Candida albicans ABC (ATP-binding cassette) protein Cdr1, overexpressed in Saccharomyces cerevisiae. A protease-cleavable C-terminal mGFPHis double tag with a 16-residue linker between Cdr1 and the tag was designed to facilitate the purification and detergent-screening of Cdr1.

Small-Scale Plasma Membrane Preparation for the Analysis of Candida albicans Cdr1-mGFPHis

The successful biochemical and biophysical characterization of ABC transporters depends heavily on the choice of the heterologous expression system. Over ...

The small scale plasma membrane isolation protocol and mGFPHis double tag, provide an economical, fast, reliable, and easy method to characterize membrane proteins in the eukaryotic model organism, Saccharomyces cerevisiae. The biggest advantage of this technology is the ease and speed with which membrane protein expression levels, the ATP's activities and the detergent is best suited for their purification can be determined. This technology is very user friendly.However, one important point to remember is to harvest cells as OD 600 of 2, which ensures low mitochondrial contamination and the highest possible ATPase activities. Begin by pre-culturing a single yeast colony in 10 milliliters of YPD medium at 30 degrees Celsius for seven to eight hours at 200 rotations per minute. Use 10 milliliters of pre culture to inoculate 40 milliliters of fresh YPD medium.Then incubate the cells at 30 degrees Celsius overnight at 200 rotations per minute until the cell density reaches an OD 600 of one to three. On the next day harvest 40 optical density units, or ODU, of logarithmic face cells by centrifuging at 4, 200 times G per five minutes at four degrees Celsius. Re-suspend and wash cells with 40 milliliters of ice cold sterile double distilled water.Repeat the washing using one milliliter of ice cold water with centrifugalization between washing steps. Re-suspend the pellet in one milliliter of ice cold sterile water and transfer the cell suspension into a 1.5 milliliter micro centrifuge tube pre-cooled on ice. Harvest cells at 3, 300 times G for three minutes at four degrees Celsius.Aspirate the supernatant and re-suspend the cell pellet in 500 microliters of homogenizing buffer freshly supplemented with one millimolar fenal methyl sulfa Neal fluoride, or PMSF. Store the cell suspension at minus 80 degrees Celsius until further use. Defrost the cells on ice for approximately one hour.Then add ice cold 0.5 millimeter diameter silica beads to the 500 microliters of the cell suspension to reach a total volume of one milliliter. To break the cells, vortex the cell suspension at maximum shaking intensity for one minute, for six cycles, with a three minute cooling period on ice following each cycle. After vortexing, make a thin hole at the bottom of the tube with a heated scalpel blade and collect the broken cell homogenate into another ice cold 1.5 milliliter micro centrifuge tube with a low speed spin for 10 seconds.Centrifuge the collected cell homogenate at 5, 156 times G for five minutes at four degrees Celsius to remove cell debris. Transfer 450 microliters of supernatant into an ice cold 1.5 milliliter micro centrifuge tube and add one milliliter of ice cold homogenizing buffer supplemented with one millimolar fresh PMSF. To harvest plasma membranes centrifuge the cell suspension at 17, 968 times G for one hour at four degrees Celsius.Remove the supernatant and add 100 microliters of homogenizing buffer freshly supplemented with one millimolar PMSF. Then loosen the plasma membrane pellet by stirring with the 100 microliter pipette tip and re-suspend the pellet by repeat pipetting up and down. Measure the protein concentration of the plasma membrane preparation with a protein assay kit that is compatible with buffers containing the reducing agent and detergent.Store the plasma membranes at minus 80 degrees Celsius, or keep them on ice for immediate use. Pour four to five milliliters of separating gel into the assembled gel apparatus up to two centimeters from the top. Carefully layer one to two milliliters of 0.1%SDS on top and allow the poly acrylamide gel to set for 60 minutes at room temperature.After an hour remove the 0.1%SDS layer from the polymerized separating gel and rinse the gel with double distilled water to remove traces of SDS. Pour the stacking gel mix onto the separating gel. Place a comb into the stacking gel and remove any air bubbles from around the comb.Then allow the stacking gel to set for 60 minutes at room temperature. Remove the comb and then rinse the gel slots with water. Put the gel into the gel tank and fill the gel tank to the top with running buffer.Mix five to 10 microliters of plasma membrane samples with equal volumes of two times protein loading dye and immediately load the sample mixture into individual gel slots, submerged in running buffer. Load protein molecular weight markers in the range from 10 to 245 Kilodalton into a separate slot to enable the size estimation of individual protein fragments. Perform gel electrophoresis at 200 volts until the blue loading dye reaches the bottom of the gel.Examine the gel for in-gel GFP fluorescence with a gel imaging system. Following the fluorescent imaging fix proteins in 10 to 20 milliliters of protein gel fixing solution by gentle agitation of the gel for 15 minutes at room temperature. Then rinse the twice for 10 minutes with 10 milliliters of double distilled water and place the gel in 10 milliliters of colloidal Kumasi stain solution with gentle shaking for one hour at room temperature to visualize protein bands.For improved visualization of protein bands, de-stain the gel once or twice in 20 milliliters of double distilled water for one hour before recording images with the gel imaging system. A high frequency of transformation of Saccharomyces cerevisiae A D Delta Delta was achieved with the positive control plasmid PS2. No Eurocell Prototron transformants were obtained for the negative control.About 50 URA cell prototroph CDR1-mGFPHis transformant were obtained after incubating transformed AD Delta Delta cells on CSM minus URA plates for three days. Petite transformant that cannot grow on YPG agar plates were eliminated. CDR1-mGHPHis samples with varying concentrations were quantified with in-gel fluorescence.The mGFP fluorescence intensities were linear over the entire concentration range with minimal background fluorescence. Varying the cell density indicated that breaking 40 ODU of cells yielded the highest quality of plasma membranes with the highest CDR1 ATPase activity. However, the yield of the plasma membranes increased in proportion to increasing cell densities.The ability of 31 detergents with various properties to solubilize CDR1-mGHPHis from crude plasma membranes of AD Delta Delta, CDR1-mGHPHis cells were tested with SDS page. Beta and alpha DDM And Fos-choline 13 were the best detergents to solubilize CDR1-mGHPHis. However, Fos-choline 13 cause partial hydrolysis of CDR1-mGHPHis.Crude plasma membrane protein solubilized with 1%detergent was separated using a superos six increased 10 300 GL size exclusion column. Chromatograms of Maltosides and LMNG extracted proteins showed most CDR1-mGHPHis eluding as a nicely shaped Gaussian peak at 15.5 millimeters CDR1-mGHPHis solubilized with glucose containing detergents alluded as an aggregated or broad aggregated peak. The higher peaks for DDM indicated that a large portion of DMN G solubilized CDR1-mGHPHis may be denatured.In the FSCC chromatograms for zwitterionic Fos-cholines and two non-ionic detergents only Digitonin and gave a similar chromatogram to DDM. Fos-choline 13 gave a symmetrical sharp shaped peak, but it alluded with a significantly lower elution volume than that for DDM. The optimized double tag also improve purification yield and helped determine the localization, trafficking, and thermal stability of membrane proteins.The heterologous expression technology can also be used in high throughput drug screening, and the detailed characterization of many other membrane proteins.

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