4.6 Article

The effects of formins on the conformation of subdomain 1 in actin filaments

Journal

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotobiol.2009.10.001

Keywords

Formin; Actin; fluorescence spectroscopy; fluorescence quenching; Protein conformation

Funding

  1. Hungarian Science Foundation [K60968, 77840]
  2. Hungarian National Office for Research and Technology [GVOP-3.2.1.-2004-04-0190/3.0, GVOP-3.2.1.-2004-04-0228/3.0]
  3. Wellcome Trust International Senior Research Fellowship in Biomedical Sciences

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In this study we investigated the effects of formins oil the conformation of actin filaments by using the method of fluorescence quenching Actin was labelled with IAEDANS at Cys(374) and the quencher was acrylamide The results showed that formin binding induced structural changes in the subdomain 1 of actin protomers which were reflected by greater quenching constants (K-SV) Simultaneously the fraction of the fluorophore population accessible for the quencher (alpha) decreased. These observations suggest that the conformational distribution characteristic for the actin protomers became broader after the binding of formins. for which the structural framework was provided by a more flexible protein matrix in the microenvironment of the label The effects of formins depended on the formin.actin molar ratio, and also on the ionic strength of the medium. These observations are in agreement with previous results and underline the importance of the intramolecular conformational changes induced by formins in the structure of actin filaments. (C) 2009 Elsevier B.V. All rights reserved

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