ß-TOXIN INSECTICIDE

The ß-scorpion toxin binding site as a potential target for new insecticides

 Coordinatore FRIEDRICH-ALEXANDER-UNIVERSITAT ERLANGEN NURNBERG 

 Organization address address: SCHLOSSPLATZ 4
city: ERLANGEN
postcode: 91054

contact info
Titolo: Ms.
Nome: Ulrike
Cognome: Hoffmann
Email: send email
Telefono: +49 9131 85 24043
Fax: +49 9131 85 26239

 Nazionalità Coordinatore Germany [DE]
 Totale costo 217˙824 €
 EC contributo 217˙824 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2010-IEF
 Funding Scheme MC-IEF
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-08-01   -   2013-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FRIEDRICH-ALEXANDER-UNIVERSITAT ERLANGEN NURNBERG

 Organization address address: SCHLOSSPLATZ 4
city: ERLANGEN
postcode: 91054

contact info
Titolo: Ms.
Nome: Ulrike
Cognome: Hoffmann
Email: send email
Telefono: +49 9131 85 24043
Fax: +49 9131 85 26239

DE (ERLANGEN) coordinator 217˙824.20

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

voltage    toxin    insect    site    molecular    species    toxins    bmk    electrophysiology    ion    health    sensor    insecticide       beta    it    bind    channel    scorpion    expression    sodium    thereby    resistance    binding    techniques    receptor   

 Obiettivo del progetto (Objective)

'Effective pest control is essential for human health, prosperity and food security. The development of insecticide resistance threatens agriculture and health programmes, where insect vectors spread life-threatening diseases such as malaria. Therefore there is a continuous need for new, effective and environmentally-friendly insecticides against novel molecular targets in order to circumvent resistance mechanisms. Members of the beta-scorpion toxin family display an extraordinary species-selective toxicity towards insects. beta-toxins bind with voltage-gated sodium channels but the binding determinants of the beta-toxin receptor site remain to be fully elucidated. In particular the residues which underpin the species-selectivity of toxin binding are not determined yet. I propose to elucidate the binding interactions of the insect-specific BmK IT1 beta-scorpion toxin with its receptor site on the extracellular linkers of the insect domain II voltage-sensor. I plan to use a recently-developed chimeric strategy in a combinatory mutagenesis, electrophysiology and 3D modelling approach in order to generate a description of toxin binding. I have expertise in molecular biology, computer modelling and ion channel expression. To complete my skill set as an ion channel researcher, I require practical electrophysiology experience. With this grant, I will pursue three goals: 1. Training in electrophysiology techniques. 2. Application of these techniques to study BmK IT1 binding with insect receptor site and thereby answering three questions: a: Which sodium channel function is modified by BmK IT1? b: Where on the voltage-sensor paddle does BmK IT bind? c: Does the insect S1-S2 linker modify BmK IT binding? The third goal is to develop a 3D molecular model of BmK IT interaction with the insect receptor site, thereby providing valuable structural information to enable pharmacophore modelling aiding novel insecticide design.'

Introduzione (Teaser)

Scorpion and spider toxins are difficult to produce in a laboratory or industrial setting. EU-funded researchers successfully overcame this limitation with a novel expression method in bacteria.

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