Awardees' Articles

HFSP Long-Term Fellow Lindsay Baker and colleagues

Tuesday 6th February 2018

Membrane proteins are challenging targets for structural biology as their native environment is heterogeneous and complex, so most methods rely on detergents to extract membrane proteins from their environment. As this removal can significantly alter the structure and function of these proteins, we have developed a hybrid method to study membrane proteins in their native membranes, combining high-resolution solid-state NMR spectroscopy and electron cryotomography of the same sample.


HFSP Long-Term Fellow Suphansa Sawamiphak and colleagues

Thursday 1st February 2018

The mammalian heart has very limited regenerative ability. Studying organisms capable of repairing their cardiac muscle after injury may help us to understand how to improve regeneration of the human heart. We found that in zebrafish individual cardiac muscle cells can transiently fuse with each other, allowing exchange of cell contents in response to high demand of cell proliferation during development and regeneration of the heart. Our data suggest that transient cell fusion in the heart might...


HFSP Long-Term Fellow Maria Casanova-Acebes and colleagues

Tuesday 30th January 2018

Immune cells play a major role in early breast cancer even before a tumor is detectable. Disruption of macrophages and early cancer cells interaction can prevent early dissemination and consequently, metastasis in breast cancer patients.


HFSP Program Grant holders Matthew Rockman, Boris Shraiman and Henrique Teotónio and colleagues

Monday 29th January 2018

Genetic variation is a ubiquitous feature of populations, but the nature of the connection between variation at the molecular level and variation in organismal fitness has been elusive. We tackled this problem by measuring fitness traits in a newly developed genetic mapping panel of the nematode Caenorhabditis elegans.


HFSP Program Grant holder Ian Baldwin and colleagues

Thursday 25th January 2018

Plants can effectively get rid of herbivores by "calling for help" using odors which attract animals that eat herbivores; but herbivores feed on plants day and night, and may try to escape danger by choosing to feed when their enemies are not active. By producing a combination of rapidly and slowly released odors, both of which are attractive to herbivores' enemies, plants can always "call for help" at the right time, regardless of when herbivores feed.


HFSP Program Grant holders Marcus Conrad, Valerian Kagan, Judith Klein-Seetharaman and Fulvio Ursini and colleagues

Tuesday 16th January 2018

Multicellular life developed genetically determined programs for the elimination of irreparably injured cells. While apoptosis has been in the focus of cell death for many years, the recognition that cells with accumulated excessive levels of (geno)toxic materials also die by regulated necrotic cell death routines has sparked great interest among researchers and drug makers. The latest addition to the list of these cell death programs is ferroptosis - a network of reactions engaging three major...


HFSP Program Grant holders Valentina Emiliani and Ed Boyden and colleagues

Monday 15th January 2018

A new approach that allows the spatial and temporal control of neuronal activation at a single cell level with a resolution of the order of milliseconds has been developed in the labs of HFSP grant holders Valentina Emiliani and Ed Boyden. This approach combines the development of a new type of light-sensitive protein that can be embedded in neuron cell bodies, combined with an innovative holographic light shaping approach that can focus light on a single cell using low light levels. These advances...


HFSP Long-Term Fellow Ryosuke Kojima and colleagues

Thursday 4th January 2018

Designer non-immune cells that mimic T-cell functions without the risks associated with engineered immune cells have been developed. The designer cells might become useful for next-generation cell-based cancer therapy. This study also extends available design principles to create artificial cellular functions.


HFSP Long-Term Fellow Erinc Hallacli and colleagues

Tuesday 2nd January 2018

Proteins fold into elaborate structures to execute their functions, and failure to do so causes many diseases, including neurodegenerative Alzheimer's disease and Parkinson's disease. However, cells can also use protein aggregation to their benefit, forming compartmentalized membrane-less bodies. Tracking these elaborate folding behaviors of proteins has been a challenge. We have developed a simple, yet powerful, tool to track protein folding in the cell with minimal observer interference...


HFSP Program Grant holders Abderrahmane Kaidi, Robert Grosse, Kei Miyamoto and colleagues

Friday 15th December 2017

When cells divide, they need to rebuild their nuclei and organise their genome. New HFSP-funded collaborative research reveals how cells achieve this through the unexpected involvement of filamentous actin (F-actin) inside the nucleus.