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Fast antibody fragment motion: flexible linkers act as entropic spring.
Stingaciu, Laura R; Ivanova, Oxana; Ohl, Michael; Biehl, Ralf; Richter, Dieter.
Afiliación
  • Stingaciu LR; Jülich Centre for Neutron Science JCNS, Forschungszentrum Jülich GmbH, outstation at SNS, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.
  • Ivanova O; Jülich Centre for Neutron Science JCNS, Forschungszentrum Jülich GmbH, outstation at MLZ, 85747 Garching, Germany.
  • Ohl M; Jülich Centre for Neutron Science JCNS, Forschungszentrum Jülich GmbH, outstation at SNS, Oak Ridge National Laboratory, Oak Ridge, TN 37831, USA.
  • Biehl R; Jülich Centre for Neutron Science JCNS (JCNS-1) &Institute of Complex Systems (ICS-1), Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.
  • Richter D; Jülich Centre for Neutron Science JCNS (JCNS-1) &Institute of Complex Systems (ICS-1), Forschungszentrum Jülich GmbH, 52425 Jülich, Germany.
Sci Rep ; 6: 22148, 2016 Mar 29.
Article en En | MEDLINE | ID: mdl-27020739
ABSTRACT
A flexible linker region between three fragments allows antibodies to adjust their binding sites to an antigen or receptor. Using Neutron Spin Echo Spectroscopy we observed fragment motion on a timescale of 7 ns with motional amplitudes of about 1 nm relative to each other. The mechanistic complexity of the linker region can be described by a spring model with Brownian motion of the fragments in a harmonic potential. Displacements, timescale, friction and force constant of the underlying dynamics are accessed. The force constant exhibits a similar strength to an entropic spring, with friction of the fragment matching the unbound state. The observed fast motions are fluctuations in pre-existing equilibrium configurations. The Brownian motion of domains in a harmonic potential is the appropriate model to examine functional hinge motions dependent on the structural topology and highlights the role of internal forces and friction to function.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Algoritmos / Fragmentos de Inmunoglobulinas / Simulación de Dinámica Molecular / Dominios Proteicos Límite: Humans Idioma: En Revista: Sci Rep Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Algoritmos / Fragmentos de Inmunoglobulinas / Simulación de Dinámica Molecular / Dominios Proteicos Límite: Humans Idioma: En Revista: Sci Rep Año: 2016 Tipo del documento: Article País de afiliación: Estados Unidos