Lipocalin Q83 Reveals a Dual Ligand Binding Mode with Potential Implications for the Functions of Siderocalins

Author(s)
Nicolas Coudevylle, Leonhard Geist, Georg Kontaxis, Markus Hartl, Klaus Bister, Robert Konrat
Abstract

Siderocalins are particular lipocalins that participate in the innate immune response by interfering with bacterial siderophore-mediated iron uptake. Additionally, siderocalins are involved in several physiological and pathological processes such as inflammation, iron delivery, tissue differentiation, and cancer progression. Here we show that siderocalin Q83 displays an unexpected dual ligand binding mode as it can bind enterobactin and unsaturated fatty acids simultaneously. The solution structure of the siderocalin Q83 in complex with arachidonic acid and enterobactin reveals molecular details of this novel dual binding mode and the determinants of fatty acid binding specificity. Our results suggest that Q83 is a metabolic hub linking iron and fatty acid pathways. This unexpected coupling might contribute to the pleiotropic functions of siderocalins.

Organisation(s)
Department of Structural and Computational Biology
External organisation(s)
Leopold-Franzens-Universität Innsbruck
Journal
Biochemistry
Volume
50
Pages
9192-9199
No. of pages
8
ISSN
0006-2960
DOI
https://doi.org/10.1021/bi201115q
Publication date
2011
Peer reviewed
Yes
Austrian Fields of Science 2012
106041 Structural biology
Sustainable Development Goals
SDG 3 - Good Health and Well-being
Portal url
https://ucrisportal.univie.ac.at/en/publications/83b5864f-e111-4b5f-8799-abc8be5b0f54