New therapeutic approaches to osteoporosis: targeting the osteoclast v-atpase

Informacje na temat projektu

MIVASE

Identyfikator umowy o grant: QLG1-CT-2000-01801

Projekt został zamknięty

Data rozpoczęcia 1 Grudnia 2000

Data zakończenia 30 Listopada 2004

Finansowanie w ramach

• Specific Programme for research, technological development and demonstration on "Quality of life and management of living resources", 1998-2002

Koszt całkowity

€ 2 253 153,00

Wkład UE

€ 2 253 153,00

Koordynowany przez

UNIVERSITY OF LEEDS
United Kingdom

CORDIS oferuje możliwość skorzystania z odnośników do publicznie dostępnych publikacji i rezultatów projektów realizowanych w ramach programów ramowych HORYZONT.

Odnośniki do rezultatów i publikacji związanych z poszczególnymi projektami 7PR, a także odnośniki do niektórych konkretnych kategorii wyników, takich jak zbiory danych i oprogramowanie, są dynamicznie pobierane z systemu OpenAIRE .

Rezultaty

Antibody effective in inhibiting extracellular acidification

Antibodies have been developed which show high specificity towards the specific proteins expressed in osteoblasts and a range of cancer cells. One of these antibodies can inhibit bone resorption due to osteoclasts and the migration of metastatic cancer cells in culture. Patents covering these discoveries are in the process of submission. The results have clear potential for immunotherapeutic approaches to osteoporosis and cancer.

Structural studies have progressed knowledge on the organisation and subunit association of the stalk and membrane sector of the V-H+-ATPase complex

The identification of the binding sites for natural inhibitors of the enzyme complex and the structural characterisation of the proteins involved will both aid targeting and development of compounds for therapeutic intervention. The disposition of proteins in the membrane will further aid the availability of sites of interaction of synthetic compounds.

New compounds have been sysnthesised and developed. They inhibit the vacuolar H+ ATPase and have been useful in both ESR and fluorescence experiments for determining the approximate site on the prote

A range of chemcial compounds have been synthesised which are able to inhibit the enzyme complex. Some represent quite new approaches to interfering with the mechanism of action of the enzyme. These compounds may have value as leads in the development of therapeutic approaches to osteoporosis and cancer.

The new inhibitors have been tested for inhibitory efficacy in yeast and osteoclasts. Assays for the effects in osteoclasts were developed as part of the project

A range of chemcial compounds have been synthesised which are able to inhibit the enzyme complex. Some represent quite new approaches to interfering with the mechanism of action of the enzyme. These compounds may have value as leads in the development of therapeutic approaches to osteoporosis and cancer.

Specific antibodies have been developed which increase our understanding of the topographical arrangement of a major intramembranous subunit

Antibodies have been developed which show high specificity towards the specific proteins expressed in osteoblasts and a range of cancer cells. One of these antibodies can inhibit bone resorption due to osteoclasts and the migration of metastatic cancer cells in culture. Patents covering these discoveries are in the process of submission. The results have clear potential for immunotherapeutic approaches to osteoporosis and cancer.

Cell biological work has revealed the location and processing of the complex and indicated that one of the isoforms of part of the intramembrane proton channel is probably involved in direction

Subunit a3 the largest of the integral membrane proteins which make up the enzyme complex is responsible for targeting the entire complex to the plasma membrane of osteoclasts and tumour cells. This makes the complex available to agents at the outside surface of the cells. This will facilitate the development of strategies for targetting and inhibiting the enzyme and so compromising cell function.