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Cited by 14Magnesium in Health and DiseaseCalcium signaling and nucleotide metabolismIon Channels and Receptors

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Structural insights into regulation of CNNM-TRPM7 divalent cation uptake by the small GTPase ARL15

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Mahbub, Luba, Kozlov, Guennadi, Zong, Pengyu, Lee, Emma L, Tetteh, Sandra, Nethramangalath, Thushara, Knorn, Caroline, Jiang, Jianning, Shahsavan, Ashkan, Yue, Lixia, Runnels, Loren, Gehring, Kalle·2023·eLife
DOI 10.7554/elife.86129PMC PMC10348743

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Abstract

Cystathionine-β-synthase (CBS)-pair domain divalent metal cation transport mediators (CNNMs) are an evolutionarily conserved family of magnesium transporters. They promote efflux of Mg 2+ ions on their own and influx of divalent cations when expressed with the transient receptor potential ion channel subfamily M member 7 (TRPM7). Recently, ADP-ribosylation factor-like GTPase 15 (ARL15) has been identified as CNNM-binding partner and an inhibitor of divalent cation influx by TRPM7. Here, we characterize ARL15 as a GTP and CNNM-binding protein and demonstrate that ARL15 also inhibits CNNM2 Mg 2+ efflux. The crystal structure of a complex between ARL15 and CNNM2 CBS-pair domain reveals the molecular basis for binding and allowed the identification of mutations that specifically block binding. A binding deficient ARL15 mutant, R95A, failed to inhibit CNNM and TRPM7 transport of Mg 2+ and Zn 2+ ions. Structural analysis and binding experiments with phosphatase of regenerating liver 2 (PRL2 or PTP4A2) showed that ARL15 and PRLs compete for binding CNNM to coordinate regulation of ion transport by CNNM and TRPM7.

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Figure 1. ADP-ribosylation factor-like GTPase 15 (ARL15) (32–197) purifies without nucleotide bound and has weak affinity for GTP. (A) UV spectra of recombinant ARL15 and the GTPase hRAS. Spectra were recorded before (blue) and after heat treatment (orange) to precipitate the protein component. Unlike hRAS, ARL15 has no nucleotide bound. (B) 1H-15N correlation NMR spectra of 100 µM ARL15 unliganded (black) and with 500 µM GTP (red). (C) Phosphorus (31P) NMR spectra of recombinant ARL15 titrated with GTP. Prior to addition of GTP, no signals are visible. GTP binds until ARL15 is saturated whereupon signals for both bound and free GTP are observed. (D) Isothermal titration calorimetry shows ARL15 binds GTP with mid-micromolar affinity.
Figure 1. ADP-ribosylation factor-like GTPase 15 (ARL15) (32–197) purifies without nucleotide bound and has weak affinity for GTP. (A) UV spectra of recombinant ARL15 and the GTPase hRAS. Spectra were recorded before (blue) and after heat treatment (orange) to precipitate the protein component. Unlike hRAS, ARL15 has no nucleotide bound. (B) 1H-15N correlation NMR spectra of 100 µM ARL15 unliganded (black) and with 500 µM GTP (red). (C) Phosphorus (31P) NMR spectra of recombinant ARL15 titrated with GTP. Prior to addition of GTP, no signals are visible. GTP binds until ARL15 is saturated whereupon signals for both bound and free GTP are observed. (D) Isothermal titration calorimetry shows ARL15 binds GTP with mid-micromolar affinity.CC BY · PubMed Central
Figure 1—figure supplement 1. ADP-ribosylation factor-like GTPase 15 (ARL15) has low intrinsic GTPase activity. (A) Procedure to detect bound nucleotide. Figure prepared with BioRender. (B) Measurement of intrinsic GTPase activity. 31P NMR spectra of 1 mM ARL15 with 2 mM GTP collected overnight at 25°C show an accumulation of free phosphate and a small (~25%) decrease in free GTP. The loss corresponds to a turnover rate of 0.000005 s–1. Notably, there is no evidence of formation of GDP, which would appear as a decrease in the β signal relative to the α and γ signals.
Figure 1—figure supplement 1. ADP-ribosylation factor-like GTPase 15 (ARL15) has low intrinsic GTPase activity. (A) Procedure to detect bound nucleotide. Figure prepared with BioRender. (B) Measurement of intrinsic GTPase activity. 31P NMR spectra of 1 mM ARL15 with 2 mM GTP collected overnight at 25°C show an accumulation of free phosphate and a small (~25%) decrease in free GTP. The loss corresponds to a turnover rate of 0.000005 s–1. Notably, there is no evidence of formation of GDP, which would appear as a decrease in the β signal relative to the α and γ signals.CC BY · PubMed Central
Figure 2. ADP-ribosylation factor-like GTPase 15 (ARL15) binds cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM) cystathionine-β-synthase (CBS)-pair domains. (A) Domains of ARL15 and CNNM2 proteins used in binding experiments. The four CNNM protein have the same domain organization. (B) Isothermal titration calorimetry experiment between the ARL15 GTPase domain and CNNM2 CBS-pair domain. (C) Binding affinities (Kd) between ARL15 GTPase domain and CBS-pair and cytosolic fragments of CNNM proteins measured by isothermal titration calorimetry (ITC). (D) Effect of nucleotides on the affinity of the ARL15-CNNM2 interaction measured by ITC. The CNNM2 T568I mutant, which is unable to bind ATP, bound ARL15 with the same affinity as the wild-type CNNM2 CBS-pair domain but did not show increased affinity upon addition of ATP.
Figure 2. ADP-ribosylation factor-like GTPase 15 (ARL15) binds cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM) cystathionine-β-synthase (CBS)-pair domains. (A) Domains of ARL15 and CNNM2 proteins used in binding experiments. The four CNNM protein have the same domain organization. (B) Isothermal titration calorimetry experiment between the ARL15 GTPase domain and CNNM2 CBS-pair domain. (C) Binding affinities (Kd) between ARL15 GTPase domain and CBS-pair and cytosolic fragments of CNNM proteins measured by isothermal titration calorimetry (ITC). (D) Effect of nucleotides on the affinity of the ARL15-CNNM2 interaction measured by ITC. The CNNM2 T568I mutant, which is unable to bind ATP, bound ARL15 with the same affinity as the wild-type CNNM2 CBS-pair domain but did not show increased affinity upon addition of ATP.CC BY · PubMed Central
Figure 3. Crystal structure of ADP-ribosylation factor-like GTPase 15 (ARL15) bound to the cystathionine-β-synthase (CBS)-pair domain of CBS-pair domain divalent metal cation transport mediator 2 (CNNM2). (A) Domain organization of the proteins. (B) Sequences of the fragments crystallized and residues mutated. The typical GTPase motifs are indicated for ARL15. Within the CNNM2 CBS-pair domain, the CBS1 and CBS2 motifs are singly and doubly underlined. (C) Crystal structure of two ARL15 molecules bound to a CBS-pair domain dimer. There are two distinct interfaces (gray lines) between the ARL15 and CBS-pair monomers. (D) Detail of intermolecular contacts between ARL15 and the CNNM2 CBS-pair domain. (E) Interfacial ARL15 residues tested by mutagenesis. (F) Interfacial CNNM2 residues tested by mutagenesis.
Figure 3. Crystal structure of ADP-ribosylation factor-like GTPase 15 (ARL15) bound to the cystathionine-β-synthase (CBS)-pair domain of CBS-pair domain divalent metal cation transport mediator 2 (CNNM2). (A) Domain organization of the proteins. (B) Sequences of the fragments crystallized and residues mutated. The typical GTPase motifs are indicated for ARL15. Within the CNNM2 CBS-pair domain, the CBS1 and CBS2 motifs are singly and doubly underlined. (C) Crystal structure of two ARL15 molecules bound to a CBS-pair domain dimer. There are two distinct interfaces (gray lines) between the ARL15 and CBS-pair monomers. (D) Detail of intermolecular contacts between ARL15 and the CNNM2 CBS-pair domain. (E) Interfacial ARL15 residues tested by mutagenesis. (F) Interfacial CNNM2 residues tested by mutagenesis.CC BY · PubMed Central
Figure 3—figure supplement 1. Structural comparison of the cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) cystathionine-β-synthase (CBS)-pair domain dimerization when (A) bound to ADP-ribosylation factor-like GTPase 15 (ARL15) (green), (B) bound to Mg-ATP (red, PDB code 4P1O), (C) no ligand bound (brown, 4IYS), and (D) T568I mutant (blue, 4IY4).
Figure 3—figure supplement 1. Structural comparison of the cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) cystathionine-β-synthase (CBS)-pair domain dimerization when (A) bound to ADP-ribosylation factor-like GTPase 15 (ARL15) (green), (B) bound to Mg-ATP (red, PDB code 4P1O), (C) no ligand bound (brown, 4IYS), and (D) T568I mutant (blue, 4IY4).CC BY · PubMed Central
Figure 3—figure supplement 2. Comparison of ADP-ribosylation factor-like GTPase 15 (ARL15) to related small GTPases. (A) Sequence alignment of human ARL15 and other ARL/ARF GTPases. The glutamine residue in the G3 motif that is alanine in ARL15 is boxed. (B) Structural comparison of ARL15 (cyan) to small GTPases: ARL2 (pink, PDB code 4GOK), ARL3 (orange, 3BH6), ARF1 (olive, 1O3Y), ARF6 (violet, 4KAX).
Figure 3—figure supplement 2. Comparison of ADP-ribosylation factor-like GTPase 15 (ARL15) to related small GTPases. (A) Sequence alignment of human ARL15 and other ARL/ARF GTPases. The glutamine residue in the G3 motif that is alanine in ARL15 is boxed. (B) Structural comparison of ARL15 (cyan) to small GTPases: ARL2 (pink, PDB code 4GOK), ARL3 (orange, 3BH6), ARF1 (olive, 1O3Y), ARF6 (violet, 4KAX).CC BY · PubMed Central
Figure 4. Mutagenesis of ADP-ribosylation factor-like GTPase 15 (ARL15) confirms the cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM)-binding site. Pulldowns of recombinant WT and mutant ARL15 GTPase domains (residues 32–197) by (A) GST-CNNM2 cystathionine-β-synthase (CBS)-pair domain (residues 429–584), (B) GST-CNNM3 CBS-pair domain (residues 299–452), (C) GST-CNNM4 CBS-pair domain (residues 356–511). (D) Isothermal titration of mutants of ARL15 GTPase domain and CNNM2 CBS-pair domain. (E) CNNM2 binding affinities (Kd) of ARL15 GTPase mutants measured by isothermal titration calorimetry (ITC). (F) Pulldown of wild-type ARL15 (WT) and the indicated mutants expressed in HEK-293T cells by GST-fused CNNM2 CBS-pair domain. (G) Co-immunoprecipitation of FLAG-tagged ARL15 with native CNNM3 shows that the ARL15 R95A mutation fully blocks binding. No ARL15, untransfected; WT, wild-type.
Figure 4. Mutagenesis of ADP-ribosylation factor-like GTPase 15 (ARL15) confirms the cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM)-binding site. Pulldowns of recombinant WT and mutant ARL15 GTPase domains (residues 32–197) by (A) GST-CNNM2 cystathionine-β-synthase (CBS)-pair domain (residues 429–584), (B) GST-CNNM3 CBS-pair domain (residues 299–452), (C) GST-CNNM4 CBS-pair domain (residues 356–511). (D) Isothermal titration of mutants of ARL15 GTPase domain and CNNM2 CBS-pair domain. (E) CNNM2 binding affinities (Kd) of ARL15 GTPase mutants measured by isothermal titration calorimetry (ITC). (F) Pulldown of wild-type ARL15 (WT) and the indicated mutants expressed in HEK-293T cells by GST-fused CNNM2 CBS-pair domain. (G) Co-immunoprecipitation of FLAG-tagged ARL15 with native CNNM3 shows that the ARL15 R95A mutation fully blocks binding. No ARL15, untransfected; WT, wild-type.CC BY · PubMed Central
Figure 4—figure supplement 1. ADP-ribosylation factor-like GTPase 15 (ARL15) mutants are properly folded. Downfield 1H NMR spectra of ARL15 GTPase domain (residues 32–197) and mutants (S94K, S94W, R95A, P130W, P163K, P163W).
Figure 4—figure supplement 1. ADP-ribosylation factor-like GTPase 15 (ARL15) mutants are properly folded. Downfield 1H NMR spectra of ARL15 GTPase domain (residues 32–197) and mutants (S94K, S94W, R95A, P130W, P163K, P163W).CC BY · PubMed Central
Figure 5. Mutagenesis of cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM) confirms conservation of ADP-ribosylation factor-like GTPase 15 (ARL15)-binding site. (A) Conservation of key ARL15-binding residues (green) in different species. (B) Conservation of ARL15-binding residues in human CNNMs. (C–F) Pulldown of recombinant GTPase domain (residues 32–197) by GST fusions with (C) CNNM1 (residues 412–568), (D) CNNM2 (residues 429–584), (E) CNNM3 (residues 299–452 and residues 299–658), (F) CNNM4 (residues 356–511 and residues 356–726). (G) Isothermal titration calorimetry (ITC) thermogram of ARL15 GTPase domain and CNNM1 cystathionine-β-synthase (CBS)-pair domain with C508F mutation shows a threefold improvement in affinity. (H) Thermograms of CNNM4 cytosolic fragment H450K and F451K mutants show no ARL15 binding.
Figure 5. Mutagenesis of cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM) confirms conservation of ADP-ribosylation factor-like GTPase 15 (ARL15)-binding site. (A) Conservation of key ARL15-binding residues (green) in different species. (B) Conservation of ARL15-binding residues in human CNNMs. (C–F) Pulldown of recombinant GTPase domain (residues 32–197) by GST fusions with (C) CNNM1 (residues 412–568), (D) CNNM2 (residues 429–584), (E) CNNM3 (residues 299–452 and residues 299–658), (F) CNNM4 (residues 356–511 and residues 356–726). (G) Isothermal titration calorimetry (ITC) thermogram of ARL15 GTPase domain and CNNM1 cystathionine-β-synthase (CBS)-pair domain with C508F mutation shows a threefold improvement in affinity. (H) Thermograms of CNNM4 cytosolic fragment H450K and F451K mutants show no ARL15 binding.CC BY · PubMed Central
Figure 5—figure supplement 1. Cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) cystathionine-β-synthase (CBS)-pair domain mutants are properly folded. 1H NMR spectra of (A) CNNM2 WT, H523K, and F524K mutants, (B) CNNM3 WT, H391K, and F392K mutants, and (C) CNNM4 WT, H450K, and F451K mutants.
Figure 5—figure supplement 1. Cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) cystathionine-β-synthase (CBS)-pair domain mutants are properly folded. 1H NMR spectra of (A) CNNM2 WT, H523K, and F524K mutants, (B) CNNM3 WT, H391K, and F392K mutants, and (C) CNNM4 WT, H450K, and F451K mutants.CC BY · PubMed Central
Figure 6. ADP-ribosylation factor-like GTPase 15 (ARL15) and phosphatases of regenerating liver (PRLs) have overlapping but distinct binding sites. (A) Overlay of the structures of the cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) complexes with ARL15 (cyan) and PRL1 (yellow, PDB code 6WUS) shows that simultaneous binding is not possible. (B) Isothermal titration calorimetry (ITC) thermogram shows no binding of ARL15 to the preformed complex of CNNM2 and PRL2. (C) 1H-15N correlation NMR spectra of 100 µM 15N-labeled ARL15 alone (top), in the presence of 100 µM CNNM2 cystathionine-β-synthase (CBS)-pair domain (middle), and after addition of 150 µM PRL2 (bottom). The ARL15 NMR signals are attenuated upon binding CNNM2 but reappear when ARL15 is displaced by PRL2. (D) ITC thermograms demonstrating that the CNNM2 D558A mutation specifically disrupts PRL2 binding. (E) ITC thermograms demonstrating that the CNNM2 H523K mutation specifically disrupts ARL15 binding.
Figure 6. ADP-ribosylation factor-like GTPase 15 (ARL15) and phosphatases of regenerating liver (PRLs) have overlapping but distinct binding sites. (A) Overlay of the structures of the cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) complexes with ARL15 (cyan) and PRL1 (yellow, PDB code 6WUS) shows that simultaneous binding is not possible. (B) Isothermal titration calorimetry (ITC) thermogram shows no binding of ARL15 to the preformed complex of CNNM2 and PRL2. (C) 1H-15N correlation NMR spectra of 100 µM 15N-labeled ARL15 alone (top), in the presence of 100 µM CNNM2 cystathionine-β-synthase (CBS)-pair domain (middle), and after addition of 150 µM PRL2 (bottom). The ARL15 NMR signals are attenuated upon binding CNNM2 but reappear when ARL15 is displaced by PRL2. (D) ITC thermograms demonstrating that the CNNM2 D558A mutation specifically disrupts PRL2 binding. (E) ITC thermograms demonstrating that the CNNM2 H523K mutation specifically disrupts ARL15 binding.CC BY · PubMed Central
Figure 6—figure supplement 1. Competition between ADP-ribosylation factor-like GTPase 15 (ARL15) and phosphatase of regenerating liver 2 (PRL2) binding to cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) is not affected by the CNNM2 T568I mutation. (A) Isothermal titration calorimetry (ITC) thermogram shows no binding of ARL15 to the preformed complex of CNNM2 T568I and PRL2. (B) 1H-15N correlation NMR spectra of 100 µM 15N-labeled ARL15 alone (top), in the presence of 100 µM CNNM2 cystathionine-β-synthase (CBS)-pair domain mutant T568I (middle), and after addition of 150 µM PRL2 (bottom). The ARL15 NMR signals are attenuated upon binding the CNNM2 T568I mutant but reappear when ARL15 is displaced by PRL2.
Figure 6—figure supplement 1. Competition between ADP-ribosylation factor-like GTPase 15 (ARL15) and phosphatase of regenerating liver 2 (PRL2) binding to cystathionine-β-synthase-pair domain divalent metal cation transport mediator 2 (CNNM2) is not affected by the CNNM2 T568I mutation. (A) Isothermal titration calorimetry (ITC) thermogram shows no binding of ARL15 to the preformed complex of CNNM2 T568I and PRL2. (B) 1H-15N correlation NMR spectra of 100 µM 15N-labeled ARL15 alone (top), in the presence of 100 µM CNNM2 cystathionine-β-synthase (CBS)-pair domain mutant T568I (middle), and after addition of 150 µM PRL2 (bottom). The ARL15 NMR signals are attenuated upon binding the CNNM2 T568I mutant but reappear when ARL15 is displaced by PRL2.CC BY · PubMed Central
Figure 7. Disruption of the cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM)-binding site blocks ADP-ribosylation factor-like GTPase 15 (ARL15) regulation of CNNM and transient receptor potential ion channel subfamily M member 7 (TRPM7) divalent cation transport. (A) CNNM2 Mg2+ efflux is inhibited by ARL15 but not the R95A mutant. HEK-293T cells transfected with the indicated constructs were loaded with a magnesium sensitive dye and fluorescence monitored following Mg2+ depletion. The mean relative fluorescence intensities of 10 cells are shown. (B) Representative TRPM7 whole-cell currents from 293-TRPM7 cells from untransfected controls (no ARL15), wild-type, and R95A mutant ARL15 transfectants. (C) Average current density of the different groups from (B). (D) Zinc influx assay using the FluoZin-3 Zn2+ indicator was used to monitor TRPM7 function in untransfected cells or transfected with wild-type or mutant ARL15. Images shown are taken at a time point 5–10 min after application of 30 μM ZnCl2 to stimulate Zn2+ influx. (E) Cell counts of fluorescence intensity from (D). A total of 50 cells per condition were randomly selected for quantification. *** indicates a p-value of less than 0.0001.
Figure 7. Disruption of the cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM)-binding site blocks ADP-ribosylation factor-like GTPase 15 (ARL15) regulation of CNNM and transient receptor potential ion channel subfamily M member 7 (TRPM7) divalent cation transport. (A) CNNM2 Mg2+ efflux is inhibited by ARL15 but not the R95A mutant. HEK-293T cells transfected with the indicated constructs were loaded with a magnesium sensitive dye and fluorescence monitored following Mg2+ depletion. The mean relative fluorescence intensities of 10 cells are shown. (B) Representative TRPM7 whole-cell currents from 293-TRPM7 cells from untransfected controls (no ARL15), wild-type, and R95A mutant ARL15 transfectants. (C) Average current density of the different groups from (B). (D) Zinc influx assay using the FluoZin-3 Zn2+ indicator was used to monitor TRPM7 function in untransfected cells or transfected with wild-type or mutant ARL15. Images shown are taken at a time point 5–10 min after application of 30 μM ZnCl2 to stimulate Zn2+ influx. (E) Cell counts of fluorescence intensity from (D). A total of 50 cells per condition were randomly selected for quantification. *** indicates a p-value of less than 0.0001.CC BY · PubMed Central
Figure 7—figure supplement 1. Localization of HEK239T cells transfected with mCNNM2-mCherry and FLAG-ADP-ribosylation factor-like GTPase 15 (ARL15). Confocal microscopy shows that CNNM2 localizes to the plasma membrane and an intracellular compartment, possibly the Golgi apparatus. This localization is not affected by ARL15 expression. Both wild-type ARL15 and the R95A mutant localize to the plasma membrane as well as internal structures.
Figure 7—figure supplement 1. Localization of HEK239T cells transfected with mCNNM2-mCherry and FLAG-ADP-ribosylation factor-like GTPase 15 (ARL15). Confocal microscopy shows that CNNM2 localizes to the plasma membrane and an intracellular compartment, possibly the Golgi apparatus. This localization is not affected by ARL15 expression. Both wild-type ARL15 and the R95A mutant localize to the plasma membrane as well as internal structures.CC BY · PubMed Central
Figure 8. Model of regulation of cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM)-transient receptor potential ion channel subfamily M member 7 (TRPM7) complex by ADP-ribosylation factor-like GTPase 15 (ARL15) and phosphatases of regenerating liver (PRLs). CNNM on their own mediate cation efflux. PRL binding to CNNM inhibits cation efflux via CNNMs and activates TRPM7 influx. ARL15 binding to CNNM inhibits both TRPM7 and CNNM transport activity.
Figure 8. Model of regulation of cystathionine-β-synthase-pair domain divalent metal cation transport mediator (CNNM)-transient receptor potential ion channel subfamily M member 7 (TRPM7) complex by ADP-ribosylation factor-like GTPase 15 (ARL15) and phosphatases of regenerating liver (PRLs). CNNM on their own mediate cation efflux. PRL binding to CNNM inhibits cation efflux via CNNMs and activates TRPM7 influx. ARL15 binding to CNNM inhibits both TRPM7 and CNNM transport activity.CC BY · PubMed Central
Author response image 1.
Author response image 1. CC BY · PubMed Central
Author response image 2. CNNM2 CBS-pair domain color-coded, blue-to-red from the N- to C-terminus. The CBS1 (blue to green) and CBS2 motifs (yellow-green to red) fold together to form a single protein domain.
Author response image 2. CNNM2 CBS-pair domain color-coded, blue-to-red from the N- to C-terminus. The CBS1 (blue to green) and CBS2 motifs (yellow-green to red) fold together to form a single protein domain.CC BY · PubMed Central

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Metadata

Authors
Mahbub, L., Kozlov, G., Zong, P., Lee, E. L., Tetteh, S., Nethramangalath, T., Knorn, C., Jiang, J., Shahsavan, A., Yue, L., Runnels, L., & Gehring, K.
Affiliations
  • McGill University (CA)
  • UConn Health (US)
  • Rutgers, The State University of New Jersey (US)
Corresponding author
Gehring, Kalle
ORCID
Venue
eLife
Publisher
eLife Sciences Publications, Ltd
Published
2023-07-14
Volume
12
ISSN
2050-084X (ISSN-L)
DOI
10.7554/elife.86129
PMC
PMC10348743
OpenAlex
W4384339426
Cited by
14
References
3
Citations by year
2026: 3 · 2025: 8 · 2023: 3
FWCI
2.45
Type
journal article
Language
en
Open access
Licence
Locations
  • eLife (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • OSTI OAI (U.S. Department of Energy Office of Scientific and Technical Information) (submittedVersion)
  • PubMed Central (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
Funders
  • Natural Sciences and Engineering Research Council of Canada (RGPIN-2020-07195)
  • National Institutes of Health (R01HL147350)
Topics
  • Health Sciences › Nursing › Nutrition and Dietetics › Magnesium in Health and Disease
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Physiology › Calcium signaling and nucleotide metabolism
  • Life Sciences › Neuroscience › Sensory Systems › Ion Channels and Receptors
Keywords
CNNM2, TRPM7, ARL15, divalent cation transport, magnesium efflux, zinc transport, GTPase, PRL-2, ion transport regulation

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CoChat. (2026). Citation check: Structural insights into regulation of CNNM-TRPM7 divalent cation uptake by the small GTPase ARL15. https://app.cochat.ai/papers/10.7554/elife.86129
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Mahbub, L., Kozlov, G., Zong, P., Lee, E. L., Tetteh, S., Nethramangalath, T., Knorn, C., Jiang, J., Shahsavan, A., Yue, L., Runnels, L., & Gehring, K. (2023). Structural insights into regulation of CNNM-TRPM7 divalent cation uptake by the small GTPase ARL15. eLife. https://doi.org/10.7554/elife.86129