Freitag, 17. August 2018

In-solution, In-gel, FASP and S-Traping - a voyage through protein sample preparation


When it comes sample preparation in bottom-up proteomics one likes to be as fast, as reproducible and as efficient as possible. Unfortunately, most of the sample preparations are biased towards certain peptide species. In this respect  hydrophobic proteins, such as membrane proteins can be troublesome. Also one should consider sample loss during each preparation step.

However, over the years there have been a couple of techniques established, that are widely used among proteomics researchers. Each of them has advantages and disadvantages.

During In-solution protein digestion protein precipitation in chloroform/methanol is followed by re- solubilization and digestion in 8M urea. This digestion is achieved in reasonable time compared to in-gel digestion but has the disadvantage of introducing sample loss during re-solubilization step.

Second approach is the in-gel preparation, that follows the idea to entrap the protein solution within a polyacrylamid gel matrix (usually after SDS PAGE) and subsequently washing out detergents and performing  protein digestion within the gel. In gel digestion is very time consuming but it is worth though because in most cases you are ending up with a high number of PSMs.

The third technique is called FASP, which stands for filter aided sample preparation and requires about 7h hands on time. FASP tries to combined the advantages of the previously mentioned techniques. In filter aided sample preparation proteins are denatured and kept in solution by SDS. The SDS-protein mixture is subjected onto a filter cartridge, where all proteins are bonded. After an SDS-urea exchange, digestion takes place within the molecular mass cut off filter (be aware of MWCO during selection), releasing peptides whereas undigested proteins remain within the filter and would not contaminate the peptide mixture.

Depending on the geometry of the spin filter and your centrifuge over 50% of the originally used protein amount, ranging from µg to mg, can be recovered on peptide level. I found good SDS PAGE from a nature method paper which served as a control of evaluate the recovery during each step.



A rather new technique is called S-trapping, the S stands for suspension, because the proteins are trapped within a porous network made of quartz (SiO2) while being in suspension. Contaminations and salts have no binding affinity and remain in the flow through. Sample amounts ranging from ng to µg (read somewhere that 250µg is the maximum protein capacity of the silica network)
But it all starts with a common SDS step to solubilize all proteins. Afterwards this SDS micelle is partially broken up and the proteins begin to become partially denatured. This is when the quartz networks kicks in and bonds all of these particulate proteins to prevent them from aggregating with other particulate proteins. Since all the proteins are attached onto the surface of the network proteolytic digestion enzymes have an easy job to access all cleavage sites.

Quartz is a good choice since it provides low metal content (similar to type I silica in HPLC) and low peptide background during digestion. Additionally, one is able to chemically modify the silica surface to perform enrichment of certain peptides after digestion (for example with SDPD, commonly used as crosslinker, for enrichment of cysteine containing peptides, search C-S-trapping).


A recent study comparing all of these 3 sample preparation approaches indicated that S-trapping outperforms in-solution and FASP in terms of identification of unique peptides.



The S-Trapping is commercialized by a company called Protifi. There also provide a unique protease for enhanced b-ion in MSMS fragementation. Great stuff!

Keine Kommentare:

Kommentar veröffentlichen