Dynamic switching mechanisms in LOV1 and LOV2 domains of plant phototropins.

ABSTRACT: LOV domains are the light-sensitive portion of plant phototropins. They absorb light through a flavin cofactor, photochemically form a covalent bond between the chromophore and a cysteine residue in the protein, and proceed to mediate activation of an attached kinase domain. Although the photoreaction itself is now well-characterized experimentally and computationally, it is still unclear how the formation of the adduct leads to kinase activation. We have performed molecular dynamics simulations on the LOV1 domain of Chlamydomonas reinhardtii and the LOV2 domain of Avena sativa, both before and after the photoreaction, to answer this question. The extensive simulations, over 240 ns in duration, reveal significant differences in how the LOV1 and LOV2 domains respond to photoactivation. The

SUBMITTER: Freddolino PL 

PROVIDER: S-EPMC1630464 | biostudies-literature | 2006 Nov

REPOSITORIES: biostudies-literature