Authors
Guanhu Bao, Matthew Clifton, Trisha M Hoette, Kiyoshi Mori, Shi-Xian Deng, Andong Qiu, Melanie Viltard, David Williams, Neal Paragas, Thomas Leete, Ritwij Kulkarni, Xiangpo Li, Belinda Lee, Avtandil Kalandadze, Adam J Ratner, Juan Carlos Pizarro, Kai M Schmidt-Ott, Donald W Landry, Kenneth N Raymond, Roland K Strong, Jonathan Barasch
Publication date
2010/8
Journal
Nature chemical biology
Volume
6
Issue
8
Pages
602-609
Publisher
Nature Publishing Group US
Description
The lipocalins are secreted proteins that bind small organic molecules. Scn-Ngal (also known as neutrophil gelatinase associated lipocalin, siderocalin, lipocalin 2) sequesters bacterial iron chelators, called siderophores, and consequently blocks bacterial growth. However, Scn-Ngal is also prominently expressed in aseptic diseases, implying that it binds additional ligands and serves additional functions. Using chemical screens, crystallography and fluorescence methods, we report that Scn-Ngal binds iron together with a small metabolic product called catechol. The formation of the complex blocked the reactivity of iron and permitted its transport once introduced into circulation in vivo. Scn-Ngal then recycled its iron in endosomes by a pH-sensitive mechanism. As catechols derive from bacterial and mammalian metabolism of dietary compounds, the Scn-Ngal–catechol–Fe(III) complex represents an unforeseen …
Total citations
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Scholar articles
G Bao, M Clifton, TM Hoette, K Mori, SX Deng, A Qiu… - Nature chemical biology, 2010