PS-DVB Monolithic Columns Applied in A Microcolumn Switching Set-up for the Analysis of Peptides and Proteins - - Chromatography Online
PS-DVB Monolithic Columns Applied in A Microcolumn Switching Set-up for the Analysis of Peptides and Proteins

The Application Notebook

Figure 1: Direct injection (b) vs microcolumn switching with monolithic trap column of a cytochrome c digest (a) with 1 pmol injected.
Polystyrene-divinylbenzene (PS-DVB) trap columns have been evaluated for microcolumn switching applications. In contrast to traditional stationary phases, which consist of packed particles, the monolithic separation medium is made of a continuous, rigid polymeric rod with a porous structure. The absence of intraparticular void volume increases separation efficiency, allowing for faster separations. Column lifetime is higher compared to packed columns.

Figure 2: Separation of 16 intact proteins (5 ng each injected) on a monolithic capillary column after preconcentration on a monolithic trap column.
This article demonstrates that the use of monolithic trap columns for preconcentration and desalting of peptides and proteins does not negatively influence chromatographic performance or sample recovery. Sample capacity of the monolithic trap columns (200m i.d. 5 mm) is 100 pmol for both peptides and proteins.


LC system: UltiMate Plus nano LC system, Switchos
column switching module and FAMOS
autosampler (LC Packings/Dionex)

Trap column: Monolithic trap column, PS-DVB,
200-m i.d. 5 mm

Loading solvent: Water with 0.05% hepta fluorobutyric acid

Loading solvent
flow-rate: 10L/min

Analytical column: Monolithic capillary column,
PS-DVB, 200m i.d. 5 cm

Mobile phases: (a) Water, 0.05% TFA
(b) Water, acetonitrile (50:50%, v/v),
0.04% TFA

Flow-rate: 2.7L/min

Gradient: 0–70% B in 7 min for peptides
30–100% B in 25 min for proteins

temperature: 60 C

UV detection: 214 nm; 3 nL flowcell

Direct Injection vs Microcolumn Switching

Table 1: PWHH for Tryptic Peptides of Cytochrome c Separated on Monolithic Columns
The influence of the monolithic trap column on chromatographic performance was evaluated by the separation of tryptic peptides of cytochrome c. Figure 1 shows a comparison between direct injection and microcolumn switching with a monolithic trap column. Table 1 lists peak widths at half height (PWHH) for the tryptic peptides with and without preconcentration.

Protein Separation After Preconcentration Using Monolithic Columns

Figure 2 shows the separation of 16 standard proteins on a monolithic capillary column with sample loading on a monolithic trap column. PWHH were typically between 4 and 8 s.


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