Study sheds new light on cell migration

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The 3-D structure of the ELMO / DOCK2 complex, an important molecular machine that plays a crucial role in cell migration in the body, is now better understood thanks to new research by scientists in Montreal and the United Kingdom.

Working with David Barford of the University of Cambridge, scientists at the Montreal Clinical Research Institute and the Institute for Research in Immunology and Cancer of Université de Montréal, published their results last month in Nature Communications.

Cell is fundamental in many ways, including organ formation in the embryo, wound healing, or simply for the delivery of immune system cells to infection sites, the study notes.

However, when deregulated, the ELMO / DOCK complex allows aberrant cell migration and contributes to the formation of metastases, the leading cause of death in people suffering with cancer.

Now, thanks to the collaboration between IRCM researcher Jean-Francois Côté, IRIC researcher Matthew Smith, and Barford in the U.K, thenew study helps unveil the molecular detail underlying the fine-tuning of this "cell movement" machine.

Like a Transformers robot

The research team found that the ELMO / DOCK complex is capable of adopting an inactive form in which different regions of proteins fold and fit into each other, much like a Transformers robot. In this "closed" form, regions of ELMO and DOCK2 known to interact with other proteins are masked and therefore inaccessible. In its "open" form –especially when the RAC1 , the mediator of , is engaged – the complex becomes accessible. It then promotes numerous interactions with its target proteins to ensure cell migration.

"This work has generated a large amount of new information about the ELMO / DOCK complex that will stimulate many future studies around the world," said Côté, a medical professor at UdeM and vice-president for research and academic affairs at the IRCM. "This information will also provide a better understanding of the way the entire DOCK family operates."

Demystifying the mechanisms

"There are 14 ELMO and DOCK proteins, and several are implicated in human diseases," added Smith, principal investigator at IRIC and assistant professor of medicine in UdeM's department of pathology and cell biology.

"This discovery demystifies some of the fundamental mechanisms responsible for the disease. This is therefore a first step that will certainly lead to a better understanding of metastases and cancer ."

More information: Leifu Chang et al. Structure of the DOCK2−ELMO1 complex provides insights into regulation of the auto-inhibited state, Nature Communications (2020). DOI: 10.1038/s41467-020-17271-9

Journal information: Nature Communications

Citation: Study sheds new light on cell migration (2020, August 5) retrieved 18 April 2024 from
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