H2020Индивидуална стипендия2015–2017

InteractomeMalMot · Interactome of surface proteins important for Plasmodium sporozoite gliding motility

„Хоризонт 2020“ — Действия „Мария Склодовска-Кюри“

Период: 2015-05-15 → 2017-05-14
Финансиране от ЕС: 159 461 €
Участници: 1
Схема: MSCA-IF-EF-ST

Линиите свързват координатора с партньорите.

Накратко на български

Протеините на паразита Plasmodium, предизвикващ малария, се изследват за да се разбере как факторът LIMP помага за движението и закрепването му в организма. Познаването на тези механизми ще помогне за по-доброто разбиране на процесите в паразитологията.

Този кратък обзор е генериран от изкуствен интелект

Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.

Резултати накратко

Interactome of surface proteins important for Plasmodium sporozoite gliding motility

Sporozoites are the motile forms of the malaria causing parasite Plasmodium and are injected into the vertebrate host by a mosquito. Their motility is powered by the parasite’s own actin-myosin motor, which is connected to transmembrane proteins of the TRAP (thrombospondin-related anonymous protein) family which serve as force transmitters. Although many key players required for this locomotion are already known, others are still unidentified and thus their precise interplay to mediate efficient adhesion and gliding motility remains unclear. Thus, the identification of novel proteins involved in these processes is crucial for solving this mystery. This project aimed to capture interacting proteins of the recently identified novel motility factor LIMP. Understanding the main mechanisms how LIMP is involved in adhesion and gliding motility, and identifying its interacting partners are the main objectives of this project. Thus the outcome could lead to a clearer understanding of adhesion/gliding motility and thus will be beneficial for the parasitology field.

Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз

Цел на проекта

Sporozoites are the motile forms of the malaria causing parasite Plasmodium and are injected into the vertebrate host by a mosquito. Their motility is powered by the parasites own actin-myosin motor, which is connected to transmembrane proteins of the TRAP (thrombospondin-related anonymous protein) family which serve as force transmitters. This substrate-dependent locomotion is a prerequisite for tissue penetration and host cell invasion. The glycolytic enzyme aldolase was thought to be the link between actin and surface adhesins (reported in Mol Cell). However, recent data revealed that aldolase does not fulfil this role hence it is now unclear how the force is transmitted. Additionally, lack of the main surface adhesin TRAP was also found (by the host lab) to not block motility as previously reported (in Cell). Additional recent findings are challenging the model of how gliding motility works and thus highlight the importance to focus on novel proteins. One such new protein, LIMP has recently been identified in the host lab. Therefore, the principal aim presented in this proposal is the identification of the molecular function of LIMP, which shows an identical phenotype to TRAP. To this end I will generate a series of parasites strains expressing different mutated versions of LIMP which will be investigated using biophysical approaches. Moreover, I attempt to identify the proteins interacting with LIMP.

Оригинален текст от CORDIS (на английски).

Участници

UNIVERSITATSKLINIKUM HEIDELBERG · HeidelbergКоординаторГермания