scholarly journals A new parallel high-pressure packing system enables rapid multiplexed production of capillary columns

2021 ◽  
pp. 100082
Author(s):  
Johannes B. Müller-Reif ◽  
Fynn M. Hansen ◽  
Lisa Schweizer ◽  
Peter V. Treit ◽  
Philipp E. Geyer ◽  
...  
2021 ◽  
Author(s):  
Johannes B. Müller-Reif ◽  
Fynn M. Hansen ◽  
Lisa Schweizer ◽  
Peter V. Treit ◽  
Philipp E. Geyer ◽  
...  

AbstractReversed-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 µm 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.Abstract Figure


2013 ◽  
Vol 87 (11) ◽  
pp. 1905-1911 ◽  
Author(s):  
A. Yu. Kanat’eva ◽  
A. A. Korolev ◽  
M. E. Dianov ◽  
A. A. Kurganov

1978 ◽  
Vol 148 (2) ◽  
pp. 500-503 ◽  
Author(s):  
E.A. Mistryukov ◽  
R.V. Golovnya ◽  
A.L. Samusenko

2018 ◽  
Vol 90 (19) ◽  
pp. 11503-11508 ◽  
Author(s):  
Evgenia Shishkova ◽  
Alexander S. Hebert ◽  
Michael S. Westphall ◽  
Joshua J. Coon

2012 ◽  
Vol 52 (6) ◽  
pp. 437-440 ◽  
Author(s):  
A. A. Korolev ◽  
V. E. Shiryaeva ◽  
M. E. Dianov ◽  
T. P. Popova ◽  
A. A. Kurganov

2013 ◽  
Vol 1304 ◽  
pp. 177-182 ◽  
Author(s):  
Axel Vaast ◽  
Lucie Nováková ◽  
Gert Desmet ◽  
Björn de Haan ◽  
Remco Swart ◽  
...  

2013 ◽  
Vol 1315 ◽  
pp. 162-166 ◽  
Author(s):  
A.A. Kurganov ◽  
A.A. Korolev ◽  
V.E. Shiryaeva ◽  
T.P. Popova ◽  
A.Yu. Kanateva

Author(s):  
Marek Malecki ◽  
James Pawley ◽  
Hans Ris

The ultrastructure of cells suspended in physiological fluids or cell culture media can only be studied if the living processes are stopped while the cells remain in suspension. Attachment of living cells to carrier surfaces to facilitate further processing for electron microscopy produces a rapid reorganization of cell structure eradicating most traces of the structures present when the cells were in suspension. The structure of cells in suspension can be immobilized by either chemical fixation or, much faster, by rapid freezing (cryo-immobilization). The fixation speed is particularly important in studies of cell surface reorganization over time. High pressure freezing provides conditions where specimens up to 500μm thick can be frozen in milliseconds without ice crystal damage. This volume is sufficient for cells to remain in suspension until frozen. However, special procedures are needed to assure that the unattached cells are not lost during subsequent processing for LVSEM or HVEM using freeze-substitution or freeze drying. We recently developed such a procedure.


Author(s):  
Robert Corbett ◽  
Delbert E. Philpott ◽  
Sam Black

Observation of subtle or early signs of change in spaceflight induced alterations on living systems require precise methods of sampling. In-flight analysis would be preferable but constraints of time, equipment, personnel and cost dictate the necessity for prolonged storage before retrieval. Because of this, various tissues have been stored in fixatives and combinations of fixatives and observed at various time intervals. High pressure and the effect of buffer alone have also been tried.Of the various tissues embedded, muscle, cartilage and liver, liver has been the most extensively studied because it contains large numbers of organelles common to all tissues (Fig. 1).


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