New Channels on Bitesize Bio

To help you find information on exactly what you need we're implementing channels, a new way to browse content

Each channel is focused on a specific technique or area and authored/presented by hand-picked authors who are experts in their field. Make sure you don't miss a thing by checking the box below for each channel that interests you.

In return we'll send you one email per month that brings you the latest from your chosen channel(s), along with free members-only content.

Check out our upcoming new channels; Flow Cytometry and Cell Culture, we'll be launching them very soon!

I would like to receive the newsletters for the following channels

Cell Culture
Flow Cytomery
Microscopy & Imaging
Next Generation Sequencing
Writing, Publishing and Presenting
Cloning & Expression


My email address is:

Agarose Gels Do Not Polymerise!

by
From the Bitesize Bio channel

I was browsing a certain website the other day when I came across a protocol that advised: “When agarose starts to cool, it undergoes what is known as polymerization”

Polymerising agarose? Someone is getting their gel matrices mixed up, and it’s not the first time I have heard this said, so it looks like some myth-busting is required.

So hunker down for a quick run down on the difference between polymerising and non-polymerising gel matrices.

Of the common gel matrices used in molecular biology, polyacrylamide, agar and agarose, polyacrylamide is the one that polymerises. I’ll deal with agarose and agar later.

Polyacrylamide gel polymerisation

Polyacrylamide, used mainly for SDS-PAGE, is a matrix formed from monomers of acrylamide and bis-acrylamide. It’s strengths are that is it chemically inert – so won’t interact with proteins as they pass through – and that it can easily and reproducibly be made with different pore sizes to produce gels with different separation properties.

The polymerisation reaction, shown in the diagram below, is a vinyl addition catalysed by free radicals. The reaction is initiated by TEMED, which induces free radical formation from ammonium persulphate (APS). The free radicals transfer electrons to the acrylamide/bisacrylamide monomers, radicalizing them and causing them to react with each other to form the polyacrylamide chain.

In the absence of bis-acrylamide, the acrylamide would polymerise into long strands, not a porous gel. But as the diagram shows, bis-acrylamide cross-links the acrylamide chains and this is what gives rise to the formation of the porous gel matrix. The amount of crosslinking, and therefore the pore size and consequent separation properties of the gel can be controlled by varying the ratio of acrylamide to bis-acrylamide.

For more information on polyacrylamide gel polymerisation see Biorad Bulletin 1156

Agarose gel formation

So what about agarose? Well, agarose – the main component of the gelatinous agar that can be isolated from certain species of seaweed – is itself a polymer. But, polymerisation is not the mechanism for agarose gel formation.

Chemically, agarose is a polysaccharide, whose monomeric unit is a disaccharide of D-galactose and 3,6-anhydro-L-galactopyranose which is shown in the diagram below.

In aqueous solutions below 35°C these polymer strands are held together in a porous gel structure by non-covalent interactions like hydrogen bonds and electrostatic interactions. Heating the solution breaks these non-covalent interactions and separates the strands. Then as the solution cools, these non-covalent interactions are re-established and the gel forms.

So agarose (and agar) gels form by gellation through hydrogen bonding and electrostatic interactions, not through polymerisation

Articles in your inbox

Enter your email to be informed when we publish more articles like this on BsB, and also get access to all of these goodies:

  • Free ebooks and audiobooks on the topics that matter to you
  • Access to Member’s-only articles and Videos
  • Advance notice of new webinars and eBooks
  • Access to make comments and ask questions on BsB



What to read next

Build a CV You Can Be Proud Of – Part I: Communication Skills

They say scientists are highly skilled… and rightly so! While many people would think that we’re shy, retiring types who sit at our lab benches obsessing over teeny-weeny molecules, science (and particularly the process of obtaining a PhD) sets us up as highly skilled members of the workforce. I can hear you all groaning as [...]

Custom Gene Synthesis: A PCR alternative.

The past few years have seen the emergence of custom gene synthesis as a useful but expensive service available for molecular biologists. Recently, the number of companies offering custom gene synthesis has exploded, pushing the cost of the service down to much more affordable levels. Custom gene synthesis derives from oligonucleotide synthesis technology, which has [...]

Howard Hughes Plugs Funding Gap for Early Career Scientists

The Howard Howard Hughes Medical Institute (HHMI) has announced a $300 million competition to support the USA’s best early career scientists in biological and medical disciplines. The recipients of the seventy available awards will be selected from researchers who have led independent laboratories for two to six years at one of the 200 eligible U.S. [...]

About the author

Nick Oswald

Nick Oswald started Bitesize Bio on a Macbook on his kitchen table in 2007 while in his 7th year of working as a molecular biologist in biotech. He made it his day job in 2010 and has been loving it ever since.

What do you think?

Subscribe to Channels

To receive information about any of our new channels click on the button below.
subscribe to the channel newsletter »

Write for us

Have a short tip, a written
article or a video you'd like
to see published?
write for us »