25 June 2020, by MIN-Dekanat
Photo: Paul-Christian Burda and Thomas Crosskey
Crystal structure of tetrameric lipocalin in addition to live-cell microscopy pictures of malaria parasites expressing the fluorescently tagged lipocalin that accumulates in the parasitophorous and food vacuoles.
For the first time, scientists have identified a lipocalin protein in the malaria parasite Plasmodium falciparum. The discovery helps to better understand the life cycle of the parasite that is a major health burden in large regions of the world. The cooperation between the groups of Tim Gilberger from CSSB (Cellular Parasitology Department at Bernhard Nocht Institute for Tropical Medicine/ Universität Hamburg) and Matthias Wilmanns from the Hamburg branch of the European Molecular Biology Laboratory EMBL describes the discovery in the journal Cell Reports.
With an estimated 228 million cases per year worldwide and more than 400,000 deaths, malaria remains one of the most important human health threats. There is no vaccine commercially available. While biologists have revealed many details about how the malaria parasite rapidly feeds on and transforms its host’s red blood cells, there are many unsolved mysteries surrounding the parasite’s life cycle. Using the microscopic facilities available at CSSB in combination with EMBL's X-ray beamlines, the team unraveled a small piece of this mystery with the identification and characterization of the first lipocalin in the most virulent malaria parasite species P. falciparum.
Lipocalins are a family of funnel-like proteins that channel insoluble molecules such as lipids and steroids into cells. They are present in almost every organism, associated with numerous functions and show an extreme diversity that makes them hard to identify. There were no lipocalins identified in P. falciparum. Gilberger's group focused on a single gene in the malaria parasite that was predicted to encode a protein with a lipocalin superfamily signature.
To validate the identified protein the group teamed up with Willmann’s group at EMBL Hamburg. “Lipocalins don’t have a conserved primary structure but all members of the family have a similar crystal structure,” explains EMBL's Thomas Crosskey, a co-author of the paper. “Our analysis of the protein using X-ray crystallography at the PETRA III synchrotron’s P13 beamline revealed a tetrameric structure of monomers with a classic lipocalin fold thus confirming the protein as a lipocalin.” It was named P. falciparum lipocalin (PfLCN).
The next step in understanding PfLCN required determination of its location within the malaria parasite. The scientists marked PfLCN with a green fluorescent protein and observed its location throughout the parasite's life cycle using live cell florescence microscopy techniques available at CSSB’s Advanced Light and Fluorescence Microscopy ALFM core facility. “During its growth within the red blood cell the parasite is contained in a parasitophorous vacuole and feeds on host cell hemoglobin that is metabolized in another vacuole called the food vacuole,” explains first author Paul-Christian Burda from the Bernhard Nocht Institute. “We were able to establish that PfLCN localizes to both of these vacuolar compartments.”
After identifying, confirming the structure and locating PfLCN, the scientists moved on to investigate the protein’s function within the malaria parasite. “First we needed to find out whether PfLCN plays an important role in blood stage proliferation of the parasite,” noted Burda. “To accomplish this we removed PfLCN from the parasite and observed that without the lipocalin the parasite could not replicate in its host cell anymore.”
Intrigued by its localization to the vacuolar compartments that represent intracellular interfaces vulnerable to oxidative damage, the scientists then exposed the modified parasite to a radical scavenging molecule. “We were surprised to discover that this resulted in a partial rescue,” explains Gilberger “this suggest that one important function of PfLCN might be to play a role in reducing oxidative cell damage in the malaria parasite.” Next, Gilberger's group plans to investigate what PfLCN binds to and how it interacts with other molecules such as lipids or other hydrophobic compounds.
This collaboration not only solved a small piece of the mystery surrounding how P. falciparum ensures its survival in the host’s red blood cells but also demonstrated the success of using a combination of complementary methods to generate a fuller understanding of a protein’s structure and function. “CSSB was established to allow scientist to combine the powers of X-ray crystallography at PETRA III with complimentary microscopic techniques to answer important biological questions surrounding infection,” explains Wilmanns who was CSSB’s founding director.
Text: CSSB, DESY, red.