| Literature DB >> 33436675 |
Kristyn Hayashi1, Kenton L Longenecker2, Yi-Liang Liu1, Bryan Faust1, Aditi Prashar1, Johannes Hampl1, Vincent Stoll2, Sandro Vivona3.
Abstract
Melanotransferrin (MTf) is an iron-binding member of the transferrin superfamily that can be membrane-anchored or secreted in serum. On cells, it can mediate transferrin-independent iron uptake and promote proliferation. In serum, it is a transcytotic iron transporter across the blood-brain barrier. MTf has been exploited as a drug delivery carrier to the brain and as an antibody-drug conjugate (ADC) target due to its oncogenic role in melanoma and its elevated expression in triple-negative breast cancer (TNBC). For treatment of TNBC, an MTf-targeting ADC completed a phase I clinical trial (NCT03316794). The structure of its murine, unconjugated Fab fragment (SC57.32) is revealed here in complex with MTf. The MTf N-lobe is in an active and iron-bound, closed conformation while the C-lobe is in an open conformation incompatible with iron binding. This combination of active and inactive domains displays a novel inter-domain arrangement in which the C2 subdomain angles away from the N-lobe. The C2 subdomain also contains the SC57.32 glyco-epitope, which comprises ten protein residues and two N-acetylglucosamines. Our report reveals novel features of MTf and provides a point of reference for MTf-targeting, structure-guided drug design.Entities:
Year: 2021 PMID: 33436675 PMCID: PMC7804310 DOI: 10.1038/s41598-020-79090-8
Source DB: PubMed Journal: Sci Rep ISSN: 2045-2322 Impact factor: 4.379