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The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

Structural basis for molecular recognition of folic acid by folate receptors

Open access
Chen, Chen, Ke, Jiyuan, Zhou, X. Edward, Yi, Wei, Brunzelle, Joseph S., Li, Jun, Yong, Eu-Leong, Xu, H. Eric, Melcher, Karsten·2013·Nature

Abstract

Folate receptors (FRα, FRβ and FRγ) are cysteine-rich cell-surface glycoproteins that bind folate with high affinity to mediate cellular uptake of folate. Although expressed at very low levels in most tissues, folate receptors, especially FRα, are expressed at high levels in numerous cancers to meet the folate demand of rapidly dividing cells under low folate conditions. The folate dependency of many tumours has been therapeutically and diagnostically exploited by administration of anti-FRα antibodies, high-affinity antifolates, folate-based imaging agents and folate-conjugated drugs and toxins. To understand how folate binds its receptors, we determined the crystal structure of human FRα in complex with folic acid at 2.8 Å resolution. FRα has a globular structure stabilized by eight disulphide bonds and contains a deep open folate-binding pocket comprised of residues that are conserved in all receptor subtypes. The folate pteroate moiety is buried inside the receptor, whereas its glutamate moiety is solvent-exposed and sticks out of the pocket entrance, allowing it to be conjugated to drugs without adversely affecting FRα binding. The extensive interactions between the receptor and ligand readily explain the high folate-binding affinity of folate receptors and provide a template for designing more specific drugs targeting the folate receptor system.

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Crossref · 10.1038/nature12327

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Metadata

Authors
Chen, C., Ke, J., Zhou, X. E., Yi, W., Brunzelle, J. S., Li, J., Yong, E.-L., Xu, H. E., & Melcher, K.
Venue
Nature
Published
2013-07-14
Volume
500
Issue
7463
Pages
486-489
ISSN
  • 0028-0836 (ISSN-L)
  • 1476-4687
OpenAlex
W2166984808
Cited by
694
References
2
FWCI
31.25
Type
journal article
Language
en
Open access
green

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