Selective Labelling of Cell-surface Proteins using CyDye DIGE Fluor Minimal Dyes

Summary

A simple and specific method was demonstrated for fluorescent labeling and enhanced detection of cell surface proteins without a fractionation step. Differential abundance in cell surface proteins was analyzed using two-dimensional (2-D) electrophoresis and Ettan™ DIGE technology.

Abstract

Surface proteins are central to the cell's ability to react to its environment and to interact with neighboring cells. They are known to be inducers of almost all intracellular signaling. Moreover, they play an important role in environmental adaptation and drug treatment, and are often involved in disease pathogenesis and pathology (1). Protein-protein interactions are intrinsic to signaling pathways, and to gain more insight in these complex biological processes, sensitive and reliable methods are needed for studying cell surface proteins. Two-dimensional (2-D) electrophoresis is used extensively for detection of biomarkers and other targets in complex protein samples to study differential changes. Cell surface proteins, partly due to their low abundance (1 2% of cellular proteins), are difficult to detect in a 2-D gel without fractionation or some other type of enrichment. They are also often poorly represented in 2-D gels due to their hydrophobic nature and high molecular weight (2). In this study, we present a new protocol for intact cells using CyDye DIGE Fluor minimal dyes for specific labeling and detection of this important group of proteins. The results showed specific labeling of a large number of cell surface proteins with minimal labeling of intracellular proteins. This protocol is rapid, simple to use, and all three CyDye DIGE Fluor minimal dyes (Cy 2, Cy 3 and Cy 5) can be used to label cell-surface proteins. These features allow for multiplexing using the 2-D Fluorescence Difference Gel Electrophoresis (2-D DIGE) with Ettan DIGE technology and analysis of protein expression changes using DeCyder 2-D Differential Analysis Software. The level of cell-surface proteins was followed during serum starvation of CHO cells for various lengths of time (see Table 1). Small changes in abundance were detected with high accuracy, and results are supported by defined statistical methods.

Protocol

Cell culture

1. Grow Chinese Hamster Ovary cells (CHO-K1) using standard cell culture procedures in F-12 Ham medium with GlutaMAX I containing 10% fetal calf serum, 50 U/ml penicillin, and 50 µg/ml streptomycin sulfate (Invitrogen).
2. Exchange the culture medium to serum-free media. Label the cell surface proteins were at different time points with CyDye DIGE Fluor Cy3 or Cy5 minimal dyes (see section Cell Surface Labeling, below).
3. Pool equal numbers of cells from each time point and label with CyDye DIGE Fluor Cy2. Use these as an internal standard for each 2-D gel.
4. The majority of the experiments can be performed with CHO-K1 cells, but mouse embryo fibroblasts (3T3 L1) and mouse ascites lymphoma lymphoblasts (EL4) can also used (data not shown).
5. Grow the two latter cell types in DMEM medium with GlutaMAX II, but, otherwise, use identical conditions used for the CHO-K1 cells.

Cell surface labeling

1. Carefully detach adherent cells non-enzymatically, counting and dividing into aliquots of 5–10 x106 cells. For cells growing in suspension, omit the detaching step.
2. Centrifuge the cell suspensions at about 800 x g for 5 minutes. Remove the supernatants containing the medium.
3. Wash the pellets by resuspendion in 1 ml ice cold Hank’s Balanced Salt Solution (HBSS) pH 8.5. Centrifuged at 800 x g at 4°C for 2 minutes.
4. Remove the supernatant and resuspend the cell pellet in 200 µl ice cold labeling buffer (HBSS pH 8.5, 1 M urea).
5. Label the intact cells with 600 pmol CyDye DIGE Fluor minimal dyes for 20 minutes on ice in the dark.
6. Quench the reaction by adding 20 µl 10 mM lysine. Incubate for 10 minutes.
7. Wash the surface-labeled cells twice by resuspension in 500 µl HBSS pH 7.4, followed by centrifugation at 800 x g at 4°C for 2 minutes.

Cell lysis and fractionation

1. Lyse the surface-labeled cells in 150 μl cold lysis buffer (7 M urea, 2 M thiourea, 4% CHAPS, 30 mM Tris, 5 mM magnesium acetate pH 8.5). Leave on ice for at least 1 h with occasional vortexing.
2. Centrifuge the lysates at 10 000 x g at 4°C for 5 minutes. Transfer the supernatant to a new tube. This sample is the non-fractionated sample containing all cellular proteins.
3. In parallel, wash cell pellets, as above, then fractionate (using a membrane fractionation kit, Pierce) into membrane and cytosolic fractions prior to 2-D gel electrophoresis. The membrane fraction contains internal and cell surface membrane proteins.
4. For comparison, follow the standard Ettan DIGE procedure ³, and lyse, label, and, finally, fractionate the cells. Determine the protein concentration in the samples using the 2- D Quant Kit (GE Healthcare).

2-D electrophoresis

1. Rehydrate Immobiline DryStrip gels, pH 3–11NL (24 cm) using Immobiline DryStrip Reswelling tray, 24 cm in 450 µl DeStreak Rehydration solution (0.5% IPG Buffer) overnight.
2. Apply the CyDye-labeled samples (corresponding to 50 µg total protein) to Immobiline DryStrip gels by anodic cup loading in the manifold and perform isoelectric focusing (IEF) using Ettan IPGphor II IEF System according to instructions.
3. After IEF, equilibrate the strips in two steps and place on top of large (26 x 20 cm) 12.5% polyacrylamide gels (SDS-PAGE). Overlay with 0.5% agarose (in running buffer containing bromophenol blue). Run 2-D electrophoresis using Ettan DALTtwelve Large Vertical System at 5 W/gel for 30 min, and then at 15 W/gel until the dye front reaches the bottom of the gel.

Imaging and data analysis

1. After completing 2-D electrophoresis, scan the gels for Cy2, Cy3 or Cy5 using a Typhoon 9410 Variable Mode Imager.
2. Compare spot maps from membrane fractions, cytosolic fractions, and non-fractionated samples using DeCyder 2-D Differential Analysis Software ⁴.

Post-staining

1. After imaging, silver stain the gels according to standard procedure ⁵.

Protein identification

1. Grow, harvest, wash and lyse preparative amounts (approximately 1 mg total protein from 10 x106 CHO cells) of cells, as described above for a non-fractionated sample. Use a Cy5 cell surface labeled sample (see above) as a spike, and apply together with the unlabelled preparative amounts of protein.
2. Carry out 2-D electrophoresis as described above, but this time, aplly 600 µg unlabeled cell lysate together with 50 µg cell surface labeled spike by anodic cup application. Use reference markers to allow correct spot picking, and place between the glass plates before gel casting according to recommendations ³.
3. Scan the gel in Cy5 channel to obtain the Cy5 cell surface spot map, followed by total protein staining using Deep purple total protein stain ³.
4. Match together the two spot maps using the DeCyder 2-D software and create a pick list for all the spots corresponding to the Cy 5 labeled cell surface proteins. Pick cell surface proteins using the Ettan spot handling station, extract from the gel plugs, and trypsinate using the Ettan digester. Identify using MALDI-TOF mass spectrometry.

Table 1. An Ettan DIGE experiment was performed using samples from serum depleted cells labeled according to the cell-surface protein labeling protocol in figure 1.

Sample	Time of serum depletion	Labelled with CyDye	Gel  number
1	-	Cy 3, Cy 2	1
2	30 minutes	Cy 5, Cy 2	1
3	2 hours	Cy 3, Cy 2	2
4	4 hours	Cy 5, Cy 2	2
5	16 hours	Cy 5, Cy 2	3

 

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Discussion

Protein concentration

An overview of the two labeling workflows is shown in Figure 1. Since the cells are still intact when labeled according to the cell-surface protein labeling protocol, only the cell surface proteins are exposed to the dye. In the standard Ettan DIGE protocol, the cells are lysed before labeling and proteins inside as well as outside the cell are labeled (Fig 1). The relative amount of dye to protein in the cell-surface protein labeling protocol is not known, since cell-surfa...

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Materials

Name	Company	Catalog Number	Comments
CyDye DIGE Kit, 2 nmol	Reagent	GE Healthcare	28-9345-30
2-D Quant Kit	Reagent	GE Healthcare	80-6484-51
IPG Buffer pH 3-11NL	Reagent	GE Healthcare	17-6004-40
Immobiline DryStrip pH 3-11NL, 24 cm	Reagent	GE Healthcare	17-6003-77
IPGbox	Tool	GE Healthcare	28-9334-65
IPGbox kit	Tool	GE Healthcare	28-9334-92
DeStreak Rehydration solution	Reagent	GE Healthcare	17-6003-19
Immobiline DryStrip Cover Fluid	Reagent	GE Healthcare	17-1335-01
Ettan IPGphor 3 IEF Unit	Instrument	GE Healthcare	11-0033-64
Ettan IPGphor Manifold	Instrument component	GE Healthcare	80-6498-38
Ettan DALTtwelve Gel Caster	Tool	GE Healthcare	80-6467-22
Ettan DALTtwelve Separation Unit and Power Supply/Control Unit	Instrument	GE Healthcare	80-6466-46	230 V unit: 80-6466-27
Typhoon 9410 Variable Mode Imager	Instrument	GE Healthcare	63-0055-81
Ettan Spot Picker	Instrument	GE Healthcare	18-1145-28
Ettan Digester	Instrument	GE Healthcare	18-1142-68
Ettan Spotter	Instrument	GE Healthcare	18-1142-67
Ettan MALDI-TOF	Instrument	GE Healthcare	18-1142-33
DeCyder 2-D Differential Analysis Software	Other	GE Healthcare	28-4012-01
ImageQuant Analysis Software	Other	GE Healthcare	28-9236-62
Urea	Reagent	GE Healthcare	17-1319-01
CHAPS	Reagent	GE Healthcare	17-1314-01
PlusOne Dithiothreitol (DTT)	Reagent	GE Healthcare	17-1318-01
Bromophenol Blue	Reagent	GE Healthcare	17-1329-01
Tris	Reagent	GE Healthcare	17-1321-01
Sodium Dodecylsulfate (SDS)	Reagent	GE Healthcare	17-1313-01
PlusOne Glycerol 87%	Reagent	GE Healthcare	17-1325-01
PlusOne ReadySol IEF 40% T, 3% C	Reagent	GE Healthcare	17-1310-01
PlusOne TEMED	Reagent	GE Healthcare	17-1312-01
PlusOne Ammonium Persulfate	Reagent	GE Healthcare	17-1311-01
PlusOne Glycine	Reagent	GE Healthcare	17-1323-01
2-D Sample Prep for membrane proteins	Reagent	Pierce, Thermo Scientific	89864
Streptomycin sulphate	Reagent	Invitrogen	15140-122