Biology subjects

Fernandez-Busquets, X.

Publications and source records attributed to Fernandez-Busquets, X..

3 recordsLinked to original sources

bioRxiv2025

Liquid-liquid phase separation (LLPS) as a sensing and adaptation mechanism: An evidence-based hypothesis on AP2 transcription factors in the malaria parasite

BackgroundProtein liquid-liquid phase separation (LLPS) can be driven by prion-like domains (PrLDs) inside intrinsically disordered regions (IDRs). The causing agent of the deadliest form of human malaria, Plasmodium falciparum, has abundant prion-like proteins whose aggregation is presumed to have a functional role. Multiple members of the largest family of transcription factors in P. falciparum, AP2 (PfAP2), responsible for adapting the parasite gene response in different scenarios, were found in aggregation-prone protein screenings. ResultsWe show that the PfAP2s members carry the physicochemical determinants to perform LLPS forming biomolecular condensates in vivo. The long IDRs of PfAP2s could sense changes in the cellular microenvironment, and their PrLDs could drive conformational rearrangements. PfAP2s do not function as centralizing hubs for protein-protein interaction networks, but display significant preferred interactions among themselves, establishing a large, connected subnetwork. Predictions suggest that all PfAP2s have regions to localize into LLPS-condensates, while larger PfAP2s could initiate condensation. We show that four PfAP2 members co-localize in live P. falciparum, bearing the potential to be engaged in LLPS-condensates. ConclusionWe present bioinformatics analyses and experimental data obtained in live parasites suggesting that PfAP2s are able to direct LLPS in P. falciparum. We propose a model in which sensing by the parasite of cellular stresses like host transfer, temperature changes and energy depletion, and the corresponding gene responses are driven by LLPS where the PfAP2 family plays a fundamental role. Finally, we postulate targeting PfAP2 as a new therapeutic antimalarial strategy to curb the emergence of drug-resistant parasites.

bioinformatics↗

bioRxiv2024

Proteomic analysis of the Aggregation Factor from the sponge Clathria (Microciona) prolifera suggests an ancient protein domain toolkit for allorecognition in animals

The discovery that sponges (Porifera) can fully regenerate from aggregates of dissociated cells launched them as one of the earliest experimental models for cell adhesion and allorecognition studies in animals. This process depends on an extracellular glycoprotein complex called the Aggregation Factor (AF). However, our understanding of how animal adhesion and allorecognition mechanisms first evolved is complicated by the fact that the known components of the AF are thought to be unique to sponges. We used label-free quantitative proteomics to identify additional AF components and interacting proteins in the classical model Clathria prolifera and compare them to proteins involved in cell interactions in Bilateria. Our results confirm MAFp3/p4 as the primary components of the AF, but implicate related proteins with calx-beta and wreath domains as additional components. Using AlphaFold, we unveiled close structural similarities of AF components to distant homologs in other animals, previously masked by the stark decay of sequence similarity. The wreath domain, believed to be unique to the AF, was predicted to contain a central beta-sandwich of the same organization as the vWFD domain in extracellular, gel-forming gly-coproteins in other animals. Additionally, we co-purified candidate AF-interacting proteins that share a conserved C-terminus, containing divergent Ig-like and Fn3 domains, a combination also known from IgCAMs. One of these, MAFAP1, may function to link the AF to the surface of cells. Our results highlight the existence of an ancient toolkit of conserved protein domains regulating cell-cell and cell-ECM interactions in all animals, and likely reflect a common origin of cell-adhesion and allorecognition.

biochemistry↗

bioRxiv2020

The ESCRT-III machinery participates in the production of extracellular vesicles and protein export during Plasmodium falciparum infection

Infection with Plasmodium falciparum enhances extracellular vesicles (EVs) production in parasitized red blood cells (pRBC), an important mechanism for parasite-to-parasite communication during the asexual intraerythrocytic life cycle. The endosomal sorting complex required for transport (ESCRT), and in particular the ESCRT-III sub-complex, participates in the formation of EVs in higher eukaryotes. However, RBCs have lost the majority of their organelles through the maturation process, including an important reduction in their vesicular network. Therefore, the mechanism of EV production in P. falciparum-infected RBCs remains to be elucidated. Here we demonstrate that P. falciparum possesses a functional ESCRT-III machinery that is activated by an alternative recruitment pathway involving the action of PfBro1 and PfVps32/PfVps60 proteins. Additionally, multivesicular bodies formation and membrane shedding, both reported mechanisms of EVs production, were reconstituted in the membrane model of giant unilamellar vesicles using the purified recombinant proteins. Moreover, the presence of PfVps32, PfVps60 and PfBro1 in EVs purified from a pRBC culture was confirmed by super-resolution microscopy. In accordance, disruption of the Pfvps60 gene led to a reduction in the number of the produced EVs in the KO strain when compared with the parental 3D7 strain. Overall, our results increase the knowledge on the underlying molecular mechanisms during malaria pathogenesis and demonstrate that ESCRT-III P. falciparum proteins participate in EVs production.

microbiology↗