Advertisement

Zirchrom ProTain Columns

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

7 posts Page 1 of 1
Has anyone had any experience with the ProTain columns made by Zirchrom - which are designed to:

- irreversibly bind proteins,

- but allow small molecules to pass through.

I'm wondering how well they do both the former and the latter.

Thanks

Why should anyone want to bind anything on his/her column irreversibly unless the column is to be discarded following the first injection?
All I know is; don’t offer this column to a cost-saving guru :wink:

Best Regards
Learn Innovate and Share

Dancho Dikov

I don't have any experience, but my understanding is that they are precolumns
(10-20mm?) with a reasonable protein capacity before breakthrough - IIRC, about 5 mg of protein.

They were released several years ago, but I've no idea on price. I assume they might be useful for some non-routine situations, but I haven't explored the Zirchrom site for more information.

ZirChrom ProTain is an inline protein removal system. It works in a three-fold way to bind proteins: 1. Ion exchange (neg/pos) 2. Ligand exchange (Lewis acid on zir/Lewis base of protein) 3. Hydrophobic/hydrophilic.

This three-fold attachment of proteins to ProTain is very strong and is generally on/off (conditions get proteins off quickly OR retain them strongly no in-between), making it useful as a trap for contaminating proteins. ProTain columns are compatible with all analytical columns you are currently using (silica-based, polymer-based, or hybrids). They are easy to use when the small molecule analytes are neutral or negatively charged. Positively charged small molecules can be retained by ProTain, but usually at a much weaker interaction than proteins. Appropriate conditions will need to be experimentally determined.

Loading capacity is pH and buffer dependent, it can be up to 5 mg. Regeneration of ProTain columns are possible, however, most customers find it convenient to replace them with new cartridges to save time.

I just wonder what the evidence is for a Lewis acid/base interaction.

It is just the unique surface chemistry of zirconia-based stationary phase. You can find more information on ZirChrom's or Columnex's websites.

http://www.zirchrom.com/
http://www.columnex.com/zirchrom-separations.php

Maybe someone did this, but on the sight of Zirchrom I didn´t see any evidence, also I wonder about there being Lewis acids and Broensted acids and bases there . . . . I always thought all acids and bases were described/defined by the Lewis.
7 posts Page 1 of 1

Who is online

In total there are 15 users online :: 1 registered, 0 hidden and 14 guests (based on users active over the past 5 minutes)
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am

Users browsing this forum: John Guajardo and 14 guests

Latest Blog Posts from Separation Science

Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.

Subscribe to our eNewsletter with daily, weekly or monthly updates: Food & Beverage, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.

Liquid Chromatography

Gas Chromatography

Mass Spectrometry