bioRxivBiochemistry
A new parallel high-pressure packing system enables rapid multiplexed production of capillary columns
J. B. Mueller-Reif, F. M. Hansen, L. Schweizer, P. V. Treit, P. E. Geyer, M. Mann
Abstract
Reversed-phase high performance liquid chromatography (HPLC) is the most commonly applied peptide separation technique in mass spectrometry (MS)-based proteomics. Particle-packed capillary columns are predominantly used in nano-flow HPLC systems. Despite being the broadly applied standard for many years capillary columns are still expensive and suffer from short lifetimes, particularly in combination with ultra-high-pressure chromatography systems. For this reason, and to achieve maximum performance, many laboratories produce their own in-house packed columns. This typically requires a considerable amount of time and trained personnel. Here, we present a new packing system for capillary columns enabling rapid, multiplexed column production with pressures reaching up to 3000 bar. Requiring only a conventional gas pressure supply and methanol as driving fluid, our system replaces the traditional setup of helium pressured packing bombs. By using 10x multiplexing, we have reduced the production time to just under 2 minutes for several 50 cm columns with 1.9 {micro}m particle size, speeding up the process of column production 40 to 800 times. We compare capillary columns with various inner diameters (ID) and length packed under different pressure conditions with our newly designed, broadly accessible high-pressure packing station. One sentence summaryA newly constructed parallel high-pressure packing system enables the rapid multiplexed production of capillary columns. O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=162 SRC="FIGDIR/small/433033v2_ufig1.gif" ALT="Figure 1"> View larger version (50K): org.highwire.dtl.DTLVardef@4d224forg.highwire.dtl.DTLVardef@79dd3org.highwire.dtl.DTLVardef@aa047org.highwire.dtl.DTLVardef@1a0b837_HPS_FORMAT_FIGEXP M_FIG C_FIG
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- FlashPack: Fast and simple preparation of ultra-high performance capillary columns for LC-MS
S. I. Kovalchuk, A. Rogowska-Wrzesinska, O. N. Jensen·bioRxiv·Sep 27, 2018
- A well-ordered nanoflow LC-MS/MS approach for proteome profiling using 200 cm long micro pillar array columns
J. Op De Beeck, J. Pauwels, … K. Gevaert·bioRxiv·Jul 1, 2019
- Multiphase capillarics for structurally pre-programmed sequential and parallel operations of high and low cohesion liquids
Geunyong Kim, Lan Anh Huynh, … David Juncker·bioRxiv·Sep 11, 2026
- One thousand samples per day capillary-flow LC/MS/MS for high-speed, high-sensitivity and in-depth proteomics
Ayana Tomioka, Ryota Tomioka, … Yasushi Ishihama·bioRxiv·Jun 5, 2023
- Increase the flow rate and improve hydrogen deuterium exchange mass spectrometry
D. Peterle, D. DePice, … J. R. Engen·Journal of Chromatography APeer-reviewed·Jan 1, 2023
- Are Solid Particles Ready for Prime-Time Proteomics?
Eduardo S. Kitano, Yana Demyanenko, Shabaz Mohammed·Analytical ChemistryPeer-reviewed·Aug 20, 2025