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 1: Direct injection (b) vs microcolumn switching with monolithic trap column of a cytochrome c digest (a) with 1 pmol
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
(200µm i.d. × 5 mm) is 100 pmol for both peptides and proteins.
Figure 2: Separation of 16 intact proteins (5 ng each injected) on a monolithic capillary column after preconcentration on
a monolithic trap column.
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-µm i.d. × 5 mm
Loading solvent: Water with 0.05% hepta fluorobutyric acid
Analytical column: Monolithic capillary column,
PS-DVB, 200µm i.d. × 5 cm
Mobile phases: (a) Water, 0.05% TFA
(b) Water, acetonitrile (50:50%, v/v),
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
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.
Table 1: PWHH for Tryptic Peptides of Cytochrome c Separated on Monolithic Columns
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.