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RAMP

Financiado

RAtionalising Membrane Protein crystallisation

Membrane proteins form more than 85% of drug targets, but just 600 unique membrane protein crystal structures have been determined. A better understanding of how to crystallize membrane proteins reliably is therefore urgently requ... ver más

31/08/2021

UGA

3M€

Presupuesto del proyecto: 3M€

Líder del proyecto

UNIVERSITE GRENOBLE ALPES No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Ver 11 Participantes

Financiación concedida El organismo H2020 notifico la concesión del proyecto el día 2021-08-31

Línea de financiación objetivo El proyecto se financió a través de la siguiente ayuda:

MSCA-ITN-2016: Innovative Training Networks

I+D

Cerrada hace 8 años

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11 Participantes

UGA

525.75K€ | Lider

RAGACTIVES

EUROPEAN SPALLATION SOURCE E...

263.66K€ | Participante

SURREY

273.29K€ | Participante

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Últimas noticias

29-11-2024: IDAE En las últimas 48 horas el Organismo IDAE ha otorgado 4 concesiones

29-11-2024: ECE En las últimas 48 horas el Organismo ECE ha otorgado 2 concesiones

29-11-2024: CMVAMADRID En las últimas 48 horas el Organismo CMVAMADRID ha otorgado 37 concesiones

Duración del proyecto: 53 meses Fecha Inicio: 2017-03-15
Fecha Fin: 2021-08-31

Líder del proyecto

UNIVERSITE GRENOBLE ALPES

TRL 4-5

Presupuesto del proyecto 3M€

Descripción del proyecto Membrane proteins form more than 85% of drug targets, but just 600 unique membrane protein crystal structures have been determined. A better understanding of how to crystallize membrane proteins reliably is therefore urgently required. The Innovative Training Network RAtionalising Membrane Protein crystallisation – RAMP will bring together cutting-edge physical chemistry methods for crystallisation condition control and phase diagram exploration, and the development of new lipids and screens in conjunction with industry with the most challenging biological problems. The network includes expert academic and industrial research groups in crystallisation theory, methods development, membrane protein crystallography, drug development and novel structural techniques like time-resolved and neutron crystallography. We will develop new, rational methods for crystallising membrane proteins, focusing particularly on transporters that are also interesting drug targets. The new robust crystallisation methods will also allow us to use emerging European research infrastructures like XFEL or ESS to gain insight into membrane protein function because the techniques will provide the necessary precise control of crystal size. A structured training programme organized by academia and industry together will equip the early stage researchers with the skills needed for a successful research career in the field of structural biology. Frequent secondments, research visits and meetings between early-career scientists ensure an efficient exchange of ideas and practical experiences between different groups leading to better integration of European research and innovations in structural biology. Supervision and mentoring by several senior scientists will give the researchers a strong scientific education and make them highly competitive in the work place of tomorrow. The work programme here will improve European competitiveness and advance graduate training.

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