The novel CXCL12gamma isoform encodes an unstructured cationic domain which regulates bioactivity and interaction
Cédric Laguri1, Rabia Sadir, Patricia Rueda
1Institut de Biologie Structurale, UMR 5075 CNRS CEA UJF, Grenoble, France.
Insights
The CXCL12gamma chemokine isoform exhibits high affinity for heparan sulfate (HS), ensuring strong cell surface retention. This unique binding mechanism regulates cell migration, offering new insights into chemokine function.
Area of Science:
- Biochemistry
- Molecular Biology
- Cell Biology
Background:
- CXCL12alpha regulates cell migration and tissue homing via CXCR4 and heparan sulfate (HS) interactions.
- The alternative splicing of the cxcl12 gene generates the CXCL12gamma isoform, with unexplored structure/function relationships.
- The basic residues in CXCL12gamma suggest potential specific regulation by HS.
Purpose of the Study:
- To elucidate the structure/function relationships of the CXCL12gamma chemokine isoform.
- To investigate the binding characteristics of CXCL12gamma with heparan sulfate (HS).
- To understand how CXCL12gamma's unique properties influence cell surface retention and biological activity.
Main Methods:
- Surface plasmon resonance and NMR spectroscopy were employed.
- Chemically and recombinantly produced chemokines were utilized.
- Binding affinities and complex half-lives were analyzed.
Main Results:
- CXCL12gamma possesses a structured domain and an unfolded C-terminal extension rich in basic residues (lysine and arginine).
- CXCL12gamma exhibits the highest affinity for HS ever observed (Kd = 0.9 nM) due to cooperative binding sites.
- The C-terminus of CXCL12gamma enhances complex half-life and regulates the balance between HS and CXCR4 binding.
Conclusions:
- CXCL12gamma demonstrates an unusual binding process with unprecedented high affinity for HS.
- The gamma isoform of CXCL12 is optimized for strong cell surface retention through unique structural and functional properties.
- HS differentially orchestrates CXCL12-mediated cell kinesis based on the chemokine isoform bound.
Background:
CXCL12alpha, a chemokine that importantly promotes the oriented cell migration and tissue homing of many cell types, regulates key homeostatic functions and pathological processes through interactions with its cognate receptor (CXCR4) and heparan sulfate (HS). The alternative splicing of the cxcl12 gene generates a recently identified isoform, CXCL12gamma, which structure/function relationships remain unexplored. The high occurrence of basic residues that characterize this isoform suggests however that it could feature specific regulation by HS.
Methodology/Principal Findings:
Using surface plasmon resonance and NMR spectroscopy, as well as chemically and recombinantly produced chemokines, we show here that CXCL12gamma first 68 amino acids adopt a structure closely related to the well described alpha isoform, followed by an unfolded C-terminal extension of 30 amino acids. Remarkably, 60% of these residues are either lysine or arginine, and most of them are clustered in typical HS binding sites. This provides the chemokine with the highest affinity for HP ever observed (Kd = 0.9 nM), and ensures a strong retention of the chemokine at the cell surface. This was due to the unique combination of two cooperative binding sites, one strictly required, found in the structured domain of the protein, the other one being the C-terminus which essentially functions by enhancing the half life of the complexes. Importantly, this peculiar C-terminus also regulates the balance between HS and CXCR4 binding, and consequently the biological activity of the chemokine.
Conclusions/Significance:
Together these data describe an unusual binding process that gives rise to an unprecedented high affinity between a chemokine and HS. This shows that the gamma isoform of CXCL12, which features unique structural and functional properties, is optimized to ensure its strong retention at the cell surface. Thus, depending on the chemokine isoform to which it binds, HS could differentially orchestrate the CXCL12 mediated directional cell kinesis.
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