FP5Докторантска мрежа2002–2006Включен след преглед

REAL-TIME THROMBOSIS · Molecular mechanisms of platelet-vessel wall interactions: an assessment of experimental thrombosis based on real time technologies

5РП — Човешки потенциал в науката

Период
2002-10-01 → 2006-09-30
Финансиране от ЕС
1 400 000 €
Участници
7
Схема
NET

Линиите свързват координатора с партньорите. За проекти отпреди 2014 г. CORDIS не винаги дава точни координати. Тези точки са на ниво град или държава.

Накратко на български

Молекулярните механизми, чрез които тромбоцитите се свързват със стените на кръвоносните съдове, се анализират чрез протеини и специални пептиди. Това помага за разработването на вещества, които да ограничат образуването на опасни кръвни съсиреци при сърдечно-съдови заболявания.

Този кратък обзор е генериран от изкуствен интелект

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

Цел на проекта

Thrombotic occlusion of atherosclerotic coron arteries is the common cause of acute myocardial infarction, and platelet-dependent thrombotic diseases are the first cause of death in the Westem Society. The general objective of this joint research project is to establish a highly competitive open- wall research and training infrastructure in thrombosis, based on the complementary expertise of 7 leading European laboratories, who have combined their efforts in a multidisciplinary approach to(a) investigate the molecular mechanisms underlying blood-platelet interactions with the vasculature,(b ) develop cell-type and receptor specific antagonists that will prevent uncontrolled platelet adhesion events leading to cardiovascular diseases, and(c) use state-of -the-art real time technologies to assess the efficiency of these antagonists in flowing blood conditions in vitro and in vivo.At the scientific level, our objectives are(1) to define the three-dimensional structural requirements necessary for the interaction of major prothrombogenic matrix proteins such as collagen and vWF with their respective receptors (integrins alpha2Beta1 and alphaIIBeta3, GPIb), using recombinant proteins for cocrystallisation experiments and atomic force microscopy analysis;(2) to design and synthesize small triple helical collagen-derived peptides as collagen mimetics;(3) to identify new receptor antagonists by screening parasite extracts and parasite-derived cDNA expression libraries, peptide and antibody display libraries;(4) to use platelet proteomics and MALDI- TOF technology to identify new intracellular integrin receptor ligands as potential targets for anti-thrombotic drug development, and(5) to generate new prothrombotic mice models through transgenic knock-in technology. A major objective of this network is to offer young predoctoral and postdoctoral EU-scientists high quality training in a broad spectrum of state-of-the-art technologies applied to cardio

Оригинален текст от CORDIS (на английски).

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Връзки

Данни: CORDIS, © Европейски съюз