Iron is a vital trace element for almost all organisms, and maintaining iron homeostasis is critical for human health. In mammals, the only known gatekeeper between intestinally absorbed iron and circulatory blood plasma is the membrane transporter ferroportin (Fpn). As such, dysfunction of Fpn or its regulation is a key driver of iron-related pathophysiology. This review focuses on discussing recent insights from high-resolution structural studies of the Fpn protein family. While these studies have unveiled crucial details of Fpn regulation and structural architecture, the associated functional studies have also at times provided conflicting data provoking more questions than answers. Here, we summarize key findings and illuminate important remaining questions and contradictions.
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The versatile programmability of CRISPR system has been utilized in various applications for RNA sensing. In this issue Liu and colleagues review how scientists engineer the guide RNAs (gRNAs) in CRISPR systems and create diverse strategies for designing RNA sensors. These approaches can not only detect target RNA molecules in vitro but also enable the regulation of gene expression in response to specific RNA molecules in vivo. Image provided by Yang Liu.
Structural insights into ferroportin mediated iron transport
Mika Jormakka; Structural insights into ferroportin mediated iron transport. Biochem Soc Trans 20 December 2023; 51 (6): 2143–2152. doi: https://doi.org/10.1042/BST20230594
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