NANOMECH

Protein Friction of Molecular Machines: Nanomechanics with Optical Tweezers

 Coordinatore EBERHARD KARLS UNIVERSITAET TUEBINGEN 

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 Nazionalità Coordinatore Germany [DE]
 Totale costo 1˙500˙000 €
 EC contributo 1˙500˙000 €
 Programma FP7-IDEAS-ERC
Specific programme: "Ideas" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call ERC-2010-StG_20091118
 Funding Scheme ERC-SG
 Anno di inizio 2010
 Periodo (anno-mese-giorno) 2010-12-01   -   2015-11-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    TECHNISCHE UNIVERSITAET DRESDEN

 Organization address address: HELMHOLTZSTRASSE 10
city: DRESDEN
postcode: 1069

contact info
Titolo: Ms.
Nome: Friederieke
Cognome: Noack
Email: send email
Telefono: +49 351 463 42191
Fax: +49 351 463 39742

DE (DRESDEN) beneficiary 824˙235.80
2    EBERHARD KARLS UNIVERSITAET TUEBINGEN

 Organization address address: GESCHWISTER-SCHOLL-PLATZ
city: TUEBINGEN
postcode: 72074

contact info
Titolo: Dr.
Nome: Erik
Cognome: Schäffer
Email: send email
Telefono: +49 7071 2978831
Fax: +49 7071 295042

DE (TUEBINGEN) hostInstitution 675˙764.20
3    EBERHARD KARLS UNIVERSITAET TUEBINGEN

 Organization address address: GESCHWISTER-SCHOLL-PLATZ
city: TUEBINGEN
postcode: 72074

contact info
Titolo: Mrs.
Nome: Elisabeth
Cognome: Baier
Email: send email
Telefono: +49 7071 29 78760
Fax: +49 7071 295990

DE (TUEBINGEN) hostInstitution 675˙764.20

Mappa


 Word cloud

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

molecular    self    friction    energy    mechanical    biological    organization    dynamics    efficiency    force    cells    microtubule    machines    motor    proteins    generate    motors    protein    tools   

 Obiettivo del progetto (Objective)

'Molecular machines---assemblies of macromolecules, often fueled by nucleotide hydrolysis---are fascinating devices and crucial for driving self-organization in cells. While protein components of many biological machines have been identified, and in many cases their structures have been solved, the mechanical principles that govern the operation of biological machines are poorly understood. For example, how much force can they generate; and what limits their speed and efficiency? These questions have been difficult to answer because the tools needed to study nanometer-sized machines that generate minute forces on the order of piconewtons have not been available until recently. Friction arises between proteins when they interact by making and breaking weak intermolecular bonds. When a bond breaks, the energy stored in its deformation is dissipated. Protein friction is a useful concept because it provides mechanical insight and allows for quantitative theoretical understanding of the dynamics and energy balance of mechanical cellular processes. In cells, many motor proteins often cooperate to drive motility. I will ask how friction and force-generation arise and scale with the number of motors to elucidate how collective behavior and self-organization emerge. The goals of this interdisciplinary project address the role that protein friction plays in limiting the dynamics and efficiency of microtubule-based motor proteins using a novel, combined optical tweezers and single-molecule fluorescence apparatus. In the long term, I hope that our avant-garde nanotechnological tools will be applicable to other molecular machines and that the studies on microtubule-based motors will shed light on the way that cells use energy to create pattern and order.'

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