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Danish scientists solve old blood mystery: New intriguing knowledge on blood hemoglobin

Date:
August 31, 2012
Source:
Aarhus University
Summary:
Scientists in Denmark have solved an old puzzle, which since the 1960s from many sides has been regarded as impossible to complete. The challenge was to solve the structure of the protecting protein complex that forms when hemoglobin is released from red cells and becomes toxic. This toxic release of hemoglobin occurs in many diseases affecting red cell stability, e.g. malaria.
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FULL STORY

Scientists at the research centre MEMBRANES at Aarhus University, Denmark, have completed an old puzzle, which since the 1960s from many sides has been regarded as impossible to complete. The challenge was to solve the structure of the protecting protein complex that forms when hemoglobin is released from red cells and becomes toxic. This toxic release of hemoglobin occurs in many diseases affecting red cell stability, e.g. malaria.

Technically, the most important finding in this report in Nature is a high-resolution three-dimensional mapping of the so-called 'haptoglobin-hemoglobin complex'.

"After many failing experiments, our breakthrough came when we gave up using human material and went to the local slaughterhouse to purchase pig blood. Not a particular high-technological approach, but this transition from studying human blood to blood from a species with close homology had magic effects. After running into dead ends for two years and trying out the most complex gene-technological ways to produce the right material, it suddenly worked," says Søren Kragh Moestrup, the head of the research group at Department of Biomedicine.

The discovery provides new essential information on hemoglobin that makes up most of the red cell interior. hemoglobin is an essential blood component for transport of oxygen, but it becomes toxic with potential damaging effects on tissues, in particular the kidneys, when it is released from the red cells. An excessive release can occur in many diseases, such as malaria and other infections.

However, the body has a sophisticated defence system. The first line defence is carried out by the blood protein haptoglobin, which captures hemoglobin and gates it to a receptor that engulfs the hemoglobin-haptoglobin complex. This function of the receptor named CD163 was originally discovered by the same group.

"We have now shown how this unique protein complex forms by generation of a detailed 3-dimensional map of each atom. This shows for the first time how the complex is formed and explains the tight protein association," says PhD Christian Brix Folsted Andersen. He has together with Master's student Morten Torvund-Jensen been an essential driving force in the project.

The results have also led to an unexpected discovery of a novel type of protein structure and a new patent submission on exploitation of the discovery for use in generation of a new type of synthetic proteins to be used in therapy and diagnostics.


Story Source:

The above story is based on materials provided by Aarhus University. Note: Materials may be edited for content and length.


Journal Reference:

  1. Christian Brix Folsted Andersen, Morten Torvund-Jensen, Marianne Jensby Nielsen, Cristiano Luis Pinto de Oliveira, Hans-Petter Hersleth, Niels Højmark Andersen, Jan Skov Pedersen, Gregers Rom Andersen, Søren Kragh Moestrup. Structure of the haptoglobin–haemoglobin complex. Nature, 2012; DOI: 10.1038/nature11369

Cite This Page:

Aarhus University. "Danish scientists solve old blood mystery: New intriguing knowledge on blood hemoglobin." ScienceDaily. ScienceDaily, 31 August 2012. <www.sciencedaily.com/releases/2012/08/120831104155.htm>.
Aarhus University. (2012, August 31). Danish scientists solve old blood mystery: New intriguing knowledge on blood hemoglobin. ScienceDaily. Retrieved April 28, 2015 from www.sciencedaily.com/releases/2012/08/120831104155.htm
Aarhus University. "Danish scientists solve old blood mystery: New intriguing knowledge on blood hemoglobin." ScienceDaily. www.sciencedaily.com/releases/2012/08/120831104155.htm (accessed April 28, 2015).

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