Alternative radical pairs for cryptochrome-based magnetoreception
There is growing evidence that the remarkable ability of animals, in particular birds, to sense the direction of the Earth's magnetic field relies on magnetically sensitive photochemical reactions of the protein cryptochrome. It is generally assumed that the magnetic field acts on the radical p...
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Published in: | Journal of the Royal Society interface Vol. 11; no. 95; p. 20131063 |
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Main Authors: | , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
England
The Royal Society
06-06-2014
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Subjects: | |
Online Access: | Get full text |
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Summary: | There is growing evidence that the remarkable ability of animals, in particular birds, to sense the direction of the Earth's magnetic field relies on magnetically sensitive photochemical reactions of the protein cryptochrome. It is generally assumed that the magnetic field acts on the radical pair [FAD•− TrpH•+] formed by the transfer of an electron from a group of three tryptophan residues to the photo-excited flavin adenine dinucleotide cofactor within the protein. Here, we examine the suitability of an [FAD•− Z•] radical pair as a compass magnetoreceptor, where Z• is a radical in which the electron spin has no hyperfine interactions with magnetic nuclei, such as hydrogen and nitrogen. Quantum spin dynamics simulations of the reactivity of [FAD•− Z•] show that it is two orders of magnitude more sensitive to the direction of the geomagnetic field than is [FAD•− TrpH•+] under the same conditions (50 µT magnetic field, 1 µs radical lifetime). The favourable magnetic properties of [FAD•− Z•] arise from the asymmetric distribution of hyperfine interactions among the two radicals and the near-optimal magnetic properties of the flavin radical. We close by discussing the identity of Z• and possible routes for its formation as part of a spin-correlated radical pair with an FAD radical in cryptochrome. |
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Bibliography: | Present address: Mathematical Institute, University of Oxford, Oxford OX2 6GG, UK. istex:AA12B8B1EED2813ED36F30E520DD25D4D92BBB45 ArticleID:rsif20131063 ark:/67375/V84-G2Z9H4ZS-M href:rsif20131063.pdf ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Present address: Institut für Physikalische Chemie, Albert-Ludwigs-Universität Freiburg, Freiburg, Germany. |
ISSN: | 1742-5689 1742-5662 |
DOI: | 10.1098/rsif.2013.1063 |