Fluorescent Silver Staining: A Technique to Visualize Total Protein in Polyacrylamide Gels (Scientific Article Protocol) | JoVE | Translated to Chinese (2024)

1. Preparation of the Gel

1. Perform SDS-PAGE with 4% - 12% Bis-Tris protein gels (1 mm, 15-well) using a mini gel tank filled with 2-(N-morpholino)ethanesulfonic acid (MES) buffer.
2. Dilute the samples with a mixture of distilled water, lithium dodecyl sulfate (LDS) buffer, and a sample-reducing agent.
3. Load the first lane with double the amount of stock (10 µL), followed by the normal stock amount (5 µL) and a series of twofold dilutions of the stock thereafter (13 dilutions, from 2x to 8192x).
4. Run the gel at a constant voltage of 200 V for 30 min.

2. Fixation of the Gel

1. After electrophoresis, submerge the gels in a 100 mL solution of 40% ethanol/10% acetic acid on an orbital shaker at 50 rpm at room temperature 2x (each for 30 min), or overnight at 4 °C.
2. Wash the gels 3 x 10 min each in ultrapure water in a clean container. The washing step is critical. If the acid from the fixing solution is not removed properly in the fluorogenic developing step, the excessiveTPE-4TAwill be activated by the acid and lead to strong background fluorescence in the gel.

3. Preparation of the AgNO₃Solution and Silver Impregnation of the Gel

1. To make the AgNO₃solution (0.0001%) for the impregnation, first, dissolve 0.01 g of AgNO₃in 10 mL of ultrapure water to prepare a 0.1% AgNO₃stock solution. Next, add 100 µL of the 0.1% AgNO₃stock solution into 100 mL of ultrapure water to make the working solution.
   NOTE: The AgNO₃solution should be stored in the dark before use.
2. Impregnate the gel with 100 mL of silver working solution for 1 h on an orbital shaker at 50 rpm in a sealed glass container. It is critical to perform the silver impregnation under a fume hood, protected from light with aluminium foil.
3. Wash the gel with ultrapure water (about 100 mL) in a clean container for 2 x 60 s.

4. Fluorogenic Development of the Gel

1. To prepare the dye stock solution (0.1 mM), add 3.0 mg of theTPE-4TAdye in 50 mL of ultrapure water. Sonicate the solution for a few minutes and add some NaOH solution (for example 1 M) to help dissolve the dye.
2. Check the fluorescence of the solution under a 365 nm UV lamp to ensure that the dye molecule is fully dissolved. Only weak or non-emissive solutions indicate full dissolution.
   NOTE: The dyeTPE-4TAwas synthesized following the protocol recently reported by Xieet al.TheTPE-4TAsolution is very stable and can be kept in the dark for months.
3. To prepare 100 mL of the fluorogenic developing solution (10 µM), add 10 mL of theTPE-4TAstock solution into 90 mL of ultrapure water. Check the pH of the solution using a pH meter and tune it to 7 - 9 using a sodium hydroxide solution (1 µM).
4. Transfer the gel to a clean and sealable container with 100 mL of the fluorogenic developing solution. Make sure the gel is totally immersed in the solution. Seal the container. Cover it from light and shake it overnight on an orbital shaker at 50 rpm at room temperature. Alternatively, the incubation step can also be shortened to about ~2 h by preheating the AIE developing solution to 80 °C for staining and then leaving it at room temperature.

5. Destaining and Imaging

1. Transfer the gel to a clean container and destain it in 100 mL of 10% ethanol for 30 min.
   NOTE: Water alone can be used to wash the gel. However, it is more time-efficient to use a 10% ethanol solution for the destaining. This will help to reduce the destaining process from hours to 30 min.
2. Rinse the gel in ultrapure water for 5 min.
3. Image the gel at the 365 nm channel or 302 nm channel by a gel documentation machine.