FcRL4 is an IgA receptor that primarily binds the joining chain

Immunoglobulin A (IgA) is a crucial component of the human immune system, and its interaction with receptors is essential for immune regulation. Fc-receptor-like 4 (FcRL4) is an IgA receptor that selectively binds systemic IgA containing the joining chain (J-chain). The molecular mechanism of this interaction has remained unclear. Here, we present a cryo-EM structure of FcRL4 complexed with the dIgA core (Fcα dimer and J-chain), revealing a 1:1 binding stoichiometry. FcRL4 primarily interacts with the J-chain but can nevertheless discriminate against J-chain-containing IgM through an entropic penalty mechanism. Our structure also explains why FcRL4 does not bind secretory IgA, as the secretory component would hinder FcRL4 binding. Functional studies indicate that FcRL4 lacks the ability to internalize IgA or IgA immune complex. These findings provide fresh insights into IgA biology.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2026-06-17
DOI
https://doi.org/10.1073/pnas.2600183123
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
Field-Weighted Citation Impact
0.00

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article

FcRL4 is an IgA receptor that primarily binds the joining chain

Mingqi Zhu, Junyu Xiao, Yuxin Wang, Xiaoke Yang et al.
Proceedings of the National Academy of Sciences
Monoclonal and Polyclonal Antibodies Research
article

FcRL4 is an IgA receptor that primarily binds the joining chain

Mingqi Zhu, Junyu Xiao, Yuxin Wang, Xiaoke Yang, Chen Su
article en

Abstract

Immunoglobulin A (IgA) is a crucial component of the human immune system, and its interaction with receptors is essential for immune regulation. Fc-receptor-like 4 (FcRL4) is an IgA receptor that selectively binds systemic IgA containing the joining chain (J-chain). The molecular mechanism of this interaction has remained unclear. Here, we present a cryo-EM structure of FcRL4 complexed with the dIgA core (Fcα dimer and J-chain), revealing a 1:1 binding stoichiometry. FcRL4 primarily interacts with the J-chain but can nevertheless discriminate against J-chain-containing IgM through an entropic penalty mechanism. Our structure also explains why FcRL4 does not bind secretory IgA, as the secretory component would hinder FcRL4 binding. Functional studies indicate that FcRL4 lacks the ability to internalize IgA or IgA immune complex. These findings provide fresh insights into IgA biology.

Proceedings of the National Academy of SciencesVol. 123(25)
Peking University (CN), King Center (US), Center for Life Sciences (CN)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, National Key Research and Development Program of China
Reduced inequalities, Peace, Justice and strong institutions
Openalex Percentile: Top 7%
Monoclonal and Polyclonal Antibodies Research
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