The thermo scientific pierce silver stain kit is a rapid and ultrasensitive silver stain system for protein detection in polyacrylamide gels. The stain performs consistently and reliably for both firsttime and experienced users for high, low or gradient percentage gels in singledimension or 2d format. Polyacrylamide gels are generated by the polymerization of. Louis, mo, usa introduction polyacrylamide gel electrophoresis page is a commonly used technique for analysis of proteins because of its low cost, ease of use, and high sensitivity. Silver staining of proteins in 2de gels request pdf. Silver staining protocol mass spectrometry facility. The most valuable protocols are presented in this report, including standard methods for unsupported gels and new methods devised for thin 0. International audiencesilver staining is used to detect proteins after electrophoretic separation on polyacrylamide gels.
Protein electrophoresis workflow sample preparation method selection gel and buffer preparation gels are placed in the electrophoresis cell, buffer is added, and samples are loaded. It is compatible with downstream processing such as mass spectrometry analysis after protein digestion. As proteins move through a gel in response to an electric field, the gels pore structure allows smaller proteins to travel more rapidly than larger proteins figure 2. Background staining that is associated with silver detection of proteins and nucleic acids in polyacrylamide gels has been shown to be due mostly to the amide groups in methylenebisacrylamide, a. The silverstaining procedure for detecting proteins in polyacrylamide gels has been modified and further simplified so that it is stable. Silver staining allows detection of most proteins since it is 30fold more sensitive than staining with colloidal coomassie. In recent years, numerous authors have described silver stain ing of proteins in polyacrylamide gels 2161. A silver staining method used routinely for detecting bacterial lipopolysaccharide lps in sodium dodecyl sulfatepolyacrylamide gels c. Alternate protocols describe rapid coomassie and silver staining methods, as well as fluorescent stains that are specific for phosphoproteins and glycoproteins. Silver stain kit for polyacrylamide gels product number ag25 and ag5 technical bulletin silver staining on polyacrylamide gels in both one and twodimensional gel electrophoresis systems is a highly sensitive visualization technique that allows detection of most proteins, dna and rna in the nanogram range. Improved silver staining of plant proteins, rna and dna in. Selective labelling of cellsurface proteins using cydye dige fluor minimal dyes.
It is compatible with downstream processing, such as mass spectrometry analysis after protein digestion. Silver staining is used to detect proteins after electrophoretic separation on polyacrylamide gels. Do not start with silver staining of gels of unknown protein preparations. Silver staining of protein gels md anderson cancer center. To separate proteins on the basis of their size and charge. Modified silver staining of polyacrylamide gels the proteins are separated by 1d or 2d sdspage, silver stained and analyzed by mass spectrometry. Silver stain silver staining is a more sensitive, but more difficult, method for visualizing protein bands in polyacrylamide gels. It combines excellent sensitivity in the low nanogram range with the use of very simple and cheap equipment and chemicals.
For best results and better background, we recommend using the silverquest silver staining kit. Protein gel staining methods thermo fisher scientific us. As with cbb, the binding of calconcarboxylic acid to proteins promotes the binding of silver ions and enhances silver staining 14. Improved silver staining of plant proteins, rna and dna in polyacrylamide gels. Silver staining of proteins in polyacrylamide gels mireille arxiv. In this video tutorial, we show you how to perform electrophoresis of protein samples. Silver staining of protein gels reference morrissey, j. Sds polyacrylamide gel electrophoresis is a technique that allows us to separate protein molecules by size. Fast and efficient elution of proteins from polyacrylamide. Presented here is a novel fluorescent silver staining method for proteins in polyacrylamide gels.
Silver staining techniques of polyacrylamide gels springerlink. For minigels 10 x 7 cm, use 100ml of each solution. Silver staining is an excellent technique for detecting proteins which are separated by sodium dodecyl sulfatepolyacrylamide gel electrophoresis due to its efficiency of detecting proteins present in nanograms. Disposal of electrophoresis buffer solutions and gels. Silver staining of proteins in polyacryl amide gels is a recently developed technique. However, as the electrophoretic influx of dye is constant, these gels must be destained to remove backgrounds.
The silverstaining procedure for detecting proteins in polyacrylamide gels has been modified and further simplified so that it is stable, controllable, and even more rapid than previous silverstaining methods. Silver staining of 2d electrophoresis gels springerlink. It combines excellent sensitivity in the low nanogram range whilst using very simple and cheap equipment and chemicals. Advantages of polyacrylamide gel electrophoresis page. A number of staining methods for page gels have been reported, such as coomassie brilliant blue cbb, amido black, and silver staining 24. The gel used in sdapage is polyacrylamide and agent which is used to linearize the proteins is sds. Springer nature is developing a new tool to find and evaluate protocols. Standard proteins yield the same peptide maps when extracted from coomassie and silverstained gels, as judged by electrospray and maldi mass spectrometry.
The method retains its sensitivity to proteins at the nanogram level and may be used either before or after coomassie blue staining. Modification of the silver staining technique to detect. Among the various protein detection methods following electrophoresis of polyacrylamide gels, silver staining has gained wide popularity because. The first step in purifying proteins from polyacrylamide gels is to locate the electrophoresed protein of interest in the gel. A combined coomassie bluesilver stain method has been developed in sodium dodecyl sulfate polyacrylamide gels for the detection of proteins using the. Silver staining of proteins in polyacrylamide gels. On the basis of the physicochemical principles underlying silverstaining of proteins, which are recalled in this paper, several methods of silverstaining of proteins after sds electrophoresis in polyacrylamide gels or isoelectric focusing were tested. It combines excellent sensitivity in the low nanogram range with the use of very simple and. Staining of proteins in gels with coomassie g250 without organic solvent and acetic acid. The staining exploits the selective binding of silver ion to proteins as in other silver stains but employs a highly sensitive fluorogenic silver probe tpe4ta to light up. High sensitivity silver stain for sdspage by mark schuchard, rick mehigh, and william kappel sigmaaldrich corporation, st.
Simplified method for silver staining of proteins in. Inserm u548 17 rue des martyrs, 38054 grenoble cedex 9 corresponding author email. Proteins in gels were silver stained following manufacturers recommendations. Silver staining of proteins in polyacrylamide gels request pdf. A new modification of silver staining is presented which utilizes two. The technique involves the deposition of metallic silver onto the surface of a gel at the locations of protein bands.
View enhanced pdf access article on wiley online library. This work removes a major obstacle to the lowlevel sequence analysis of proteins separated on polyacrylamide gels. Silver staining is the most sensitive colorimetric method for detecting total protein. Simplified method for silver staining of proteins in polyacrylamide.
Heterophase digestion of proteins within a polyacrylamide matrix is controlled by enzyme diffusion 3,4 and. This strategy integrates conventional silver stains and fluorescent stains. Silver staining of proteins in polyacrylamide gels mireille chevallet, sylvie luche and thierry rabilloud ceagrenoble, drdcich. The study of effects of several parameters on silver staining of proteins has led to the development of a staining method which is simple and reliable, requires only few stable solutions, and can be applied to all gel types such as sodium dodecyl sulfate sds containing polyacrylamide or isoelectric focusing gels. The silverquest silver staining kit provides a rapid and easy method to silver stain proteins in polyacrylamide gels. A guide to polyacrylamide gel electrophoresis and detection. This kit is specifically designed to provide sensitive silver staining compatible with mass spectrometry analysis. It combines excellent sensitivity in the low nanogram range with the use of. Silver staining is an excellent technique for detecting proteins which are separated by sodium dodecyl sulfatepolyacrylamide gel electrophoresis due to its efficiency of detecting proteins. Ingel digestion for mass spectrometric characterization. Page polyacrylamide gel electrophoresis, is an analytical method used to separate components of a.
Proteins from silverstained gels can be digested enzymatically and the resulting peptides analyzed and sequenced by mass spectrometry. In this tech tip, various methods for extraction elution of proteins from polyacrylamide gels are described. Silver staining protocol compatible with mass spectrometry modified from mass spectrometric sequencing of proteins from silverstained polyacrylamide gels a. A modified procedure with enhanced uniform sensitivity. Sdspage sodium dodecyl sulfate polyacrylamide gel electrophoresis is a technique used to separate the proteins according to their masses separation of macromolecules under the influence of the charge is called electrophoresis. Proteins separated on polyacrylamide gels can be transferred onto immobilized membranes blotting. Fluorescent silver staining of proteins in polyacrylamide gels. Detection of proteins in polyacrylamide gels by silver. It should be noted that while this method of staining is more sensitive, the recovery of peptides from an ingel digest is decreased and we do. It did not stain sform fractions of polyagglutinable pseudomonas aeruginosa lps or several partly deacylated alkalitreated s. Mass spectrometric sequencing of proteins silverstained. Pouring and running a protein gel by reusing commercial cassettes.
Improved staining of proteins in polyacrylamide gels including isoelectric focusing gels with clear backgrounds at nanogram sensitivity using g250 and r250. This electrophoresis process utilizes an organic fluorescence dye or an inorganic stain such as silver which is an epa regulated material to stain the nucleic acids or proteins. The introduction of silver staining of proteins in polyacrylamide gels in 1979 switzer et al. Ingel digestion for mass spectrometric characterization of proteins and proteomes.
Silver staining of proteins in polyacrylamide gels sciencedirect. Silver staining allows a substantial shortening of sample preparation time and may, therefore, be preferable over coomassie staining. Silver staining allows detection of most proteins since it is 30fold more sensitive than staining with colloidal coomassie g250. Principle and method of silver staining of proteins. Reproducible staining patterns are obtained, and the method is inexpensive, completely under the control of the user, and effective with the common polyacrylamide gel electrophoresis methods. Wash minigels in 200ml volumes of water, and agitate continuously during all steps. Fluorescent staining is a popular alternative to traditional staining procedures, mainly because it is more sensitive than coomassie staining, and often as sensitive as silver staining. Mass spectrometric sequencing of proteins from silver. These gels will typically be agarosebased or polyacrylamidebased. Silver staining is a highly sensitive method for detecting proteins and nucleic acids in polyacrylamide slab gels. Silver ions from silver nitrate in the staining reagent interact and bind with certain protein functional groups. For larger gels, increase sterling volumes appropriately to immerse gel to depth of 1cm. The low nanogram range can be reached by the protocols described here, and the method is robust.