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Spider proteins offer new insight into human heart conditions

Imperial College London Health News Jun 22, 2017

Proteins found in the muscles of tarantulas are helping scientists to understand how genetic changes can lead to serious heart conditions.

Although spiders may appear to have little in common with humans, some of the proteins that make up their muscles are similar to those in our own bodies, including muscle found in the heart.

In a study, published in the journal eLife, researchers have used spider proteins to uncover how mutations in a single gene can lead to two forms of cardiomyopathy.

The team, led by Dr James Ware from the MRC London Institute of Medical Sciences (LMS) at Imperial College London, and involving researchers from Harvard Medical School and the Venezuelan Institute for Scientific Research, believe the findings could help to make genetic tests for the condition more accurate.

At the heart of the research is a protein called myosin, a key component of heart muscle. Mutations in the gene that produce this protein can cause different forms of cardiomyopathy, which affects around 1 in 250 people in the UK.

Dr Ware and team were trying to understand why different mutations in the same gene could lead to these two different forms of the condition: dilated and hypertrophic cardiomyopathy.

The researchers used spider proteins as they enabled them to explore 3D protein structure in much greater detail than is currently possible with human models alone. They found that the long, thin muscle fibres in spiders’ legs enabled them to see not only the structure of individual proteins, but also how these proteins interact with their neighbours. In heart muscle, chains of myosin proteins form thick filaments, which sit side–by–side with thinner filaments, called actin. When a muscle contracts, the myosin fibres slide along the actin fibres to shorten the length of the muscle. It has been known that some cardiomyopathies are caused by mutations that interfere with myosin’s ability to bind to actin, changing the heart muscle contraction.

However, most previous studies have focused on single myosin molecules in isolation. In this study, the models of 3D protein structure enabled the researchers to see that as well as interacting with actin, myosin molecules interact with each other and work in pairs. These interactions are particularly important when the muscle relaxes, because they improve energy efficiency.

In the latest study, the team found that mutations which cause dilated cardiomyopathy typically alter the parts of myosin which play a role in contraction. Most mutations that cause hypertrophic cardiomyopathy also affect contraction in this way, and additionally affect these newly identified interactions, interfering with the heart’s ability to relax.

Dr Ware explained: “We’ve shown that over half of the mutations in myosin which cause hypertrophic cardiomyopathy lie in these critical binding regions. This shows the importance of mutations in this area.”

Identifying the genetic cause of a patient’s disease is important as it can help to identify whether they will pass it onto their children. Relatives of patients with cardiomyopathy often undergo regular and expensive heart tests.

The researchers hope that their findings will lead to an increase in the number of conclusive diagnoses. Those shown to have inherited the condition can be monitored and treated, perhaps even before the condition can be detected using conventional tests.
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