anti met Search Results


mouse monoclonal antibody  (R&D Systems)
93
R&D Systems mouse monoclonal antibody
Mouse Monoclonal Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse monoclonal antibody/product/R&D Systems
Average 93 stars, based on 1 article reviews
mouse monoclonal antibody - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
phospho met  (Cell Signaling Technology Inc)
95
Cell Signaling Technology Inc phospho met
Phospho Met, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/phospho met/product/Cell Signaling Technology Inc
Average 95 stars, based on 1 article reviews
phospho met - by Bioz Stars, 2026-03
95/100 stars
  Buy from Supplier
rabbit polyclonal rnmt  (Proteintech)
93
Proteintech rabbit polyclonal rnmt
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Rabbit Polyclonal Rnmt, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit polyclonal rnmt/product/Proteintech
Average 93 stars, based on 1 article reviews
rabbit polyclonal rnmt - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
met  (Proteintech)
93
Proteintech met
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Met, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/met/product/Proteintech
Average 93 stars, based on 1 article reviews
met - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
anti met antibody  (Cell Signaling Technology Inc)
96
Cell Signaling Technology Inc anti met antibody
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Anti Met Antibody, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/anti met antibody/product/Cell Signaling Technology Inc
Average 96 stars, based on 1 article reviews
anti met antibody - by Bioz Stars, 2026-03
96/100 stars
  Buy from Supplier
polyclonal primary antibody m met sp260  (Santa Cruz Biotechnology)
94
Santa Cruz Biotechnology polyclonal primary antibody m met sp260
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Polyclonal Primary Antibody M Met Sp260, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/polyclonal primary antibody m met sp260/product/Santa Cruz Biotechnology
Average 94 stars, based on 1 article reviews
polyclonal primary antibody m met sp260 - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier
lipid metabolism antibody sampler kit  (Cell Signaling Technology Inc)
93
Cell Signaling Technology Inc lipid metabolism antibody sampler kit
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Lipid Metabolism Antibody Sampler Kit, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/lipid metabolism antibody sampler kit/product/Cell Signaling Technology Inc
Average 93 stars, based on 1 article reviews
lipid metabolism antibody sampler kit - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
msra  (Proteintech)
93
Proteintech msra
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Msra, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/msra/product/Proteintech
Average 93 stars, based on 1 article reviews
msra - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier
antibodies usws  (R&D Systems)
91
R&D Systems antibodies usws
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Antibodies Usws, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/antibodies usws/product/R&D Systems
Average 91 stars, based on 1 article reviews
antibodies usws - by Bioz Stars, 2026-03
91/100 stars
  Buy from Supplier
1 ap  (Proteintech)
94
Proteintech 1 ap
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
1 Ap, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/1 ap/product/Proteintech
Average 94 stars, based on 1 article reviews
1 ap - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier
biotinylated anti human c met antibody  (R&D Systems)
94
R&D Systems biotinylated anti human c met antibody
Figure 3. Identification of <t>eIF4E-RNMT</t> complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.
Biotinylated Anti Human C Met Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/biotinylated anti human c met antibody/product/R&D Systems
Average 94 stars, based on 1 article reviews
biotinylated anti human c met antibody - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier

Image Search Results


Figure 3. Identification of eIF4E-RNMT complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.

Journal: Journal of molecular biology

Article Title: Identification and Characterization of the Interaction Between the Methyl-7-Guanosine Cap Maturation Enzyme RNMT and the Cap-Binding Protein eIF4E.

doi: 10.1016/j.jmb.2022.167451

Figure Lengend Snippet: Figure 3. Identification of eIF4E-RNMT complex binding sites and structural models. (A) m7GTP cap column chromatography for eIF4E in the presence or absence of RNMT-C. m7GTP cap-bound proteins were analysed using Western blotting. m7GTP-bound eIF4E binds to RNMT-C (lane 5, eIF4E protein was first bound to the m7GTP column, and subsequently incubated with RNMT-C); eIF4E-RNMT-C complex binds to m7GTP cap beads (labelled “complex” in lane 6, eIF4E was first incubated with RNMT-C to form a complex, and then incubated with m7GTP beads). RNMT-C does not bind directly to m7GTP beads (lane 4). 50 lM m7GTP elutes eIF4E from the m7GTP beads (lane 7) while non-methylated GTP did not affect eIF4E binding to m7GTP beads (lane 8), confirming specificity. Two percent input was used for eIF4E and RNMT-C. (B) GST-eIF4E pulldown assays for RNMT-C or RNMT-C/RAM complexes show that RNMT-C cannot bind eIF4E in the presence of RAM. (C) Close up view of binding site of RAM for RNMT-C (PDB 5E8J) used to guide RNMT mutagenesis experiments. Only interactions with the first two helices of RAM were considered (the RNMT-C lobe binding site is not important for eIF4E association (Figure 1(G). RNMT-C residues mutated are shown as sticks (single point mutants leading to a reduction in eIF4E binding are coloured red). (D) GST pulldown assay between GST-eIF4E and wild type and mutant RNMT-C proteins. (E) Lowest energy model of the complex of eIF4E with RNMT-C generated from Haddock. The catalytic site of RNMT (marked by SAH) and the cap-binding site of eIF4E are represented by arrows and far removed from the complex interface. (F, G) Superposition of the Haddock generated model of eIF4E and RNMT-C with (F) RNMT-RAM coordinates (PDB ID 5E8J) and (G) the eIF4E-BP1 (PDB ID 3U7X) coordinates.

Article Snippet: Antibodies used in Western blots Primary antibodies mouse RNMT (RNMT 3H31D12, Santa Cruz Biotechnology, Catalog No. sc517112) and mouse eIF4E (BD Biosciences, 610269), rabbit polyclonal RNMT (ProteinTech, 13743-1-AP), rabbit monoclonal 4E-BP1 (53H11, Cell Signaling Technology, #9644), rabbit polyclonal 4E-BP2, Cell Signaling Technology #2845, rabbit polyclonal RAM (FAM103A1 Polyclonal antibody, ProteinTech, 19422-1-AP) and GST Goat Polyclonal (Cytiva; catalog no. 45- 001-369).

Techniques: Binding Assay, Column Chromatography, Western Blot, Incubation, Methylation, Mutagenesis, GST Pulldown Assay, Generated

Figure 4. eIF4E-RNMT, eIF4E translation, and export complexes are mutually exclusive. (A, B) GST or GST- eIF4E pulldowns for RNMT-C in the presence or absence of 4E-BP1, 4E-BP2, 4Gp (a peptide of eIF4G, see text) (A) or LRPPRC (B). Western blots are probed as indicated. Controls for GST binding are given in Supplementary Figure S6. (C) Schematic model of summarizing the complexes explored in A and B. RNMT, LRPPRC, eIF4G and the 4EBPs all bind overlapping surfaces on eIF4E and thus form mutually exclusive complexes. The multiple arrows between the RNMT and RNA export complexes indicate that there could be other complexes between the capping and export ones depicted. Not all eIF4E complexes known are shown here for simplicity.

Journal: Journal of molecular biology

Article Title: Identification and Characterization of the Interaction Between the Methyl-7-Guanosine Cap Maturation Enzyme RNMT and the Cap-Binding Protein eIF4E.

doi: 10.1016/j.jmb.2022.167451

Figure Lengend Snippet: Figure 4. eIF4E-RNMT, eIF4E translation, and export complexes are mutually exclusive. (A, B) GST or GST- eIF4E pulldowns for RNMT-C in the presence or absence of 4E-BP1, 4E-BP2, 4Gp (a peptide of eIF4G, see text) (A) or LRPPRC (B). Western blots are probed as indicated. Controls for GST binding are given in Supplementary Figure S6. (C) Schematic model of summarizing the complexes explored in A and B. RNMT, LRPPRC, eIF4G and the 4EBPs all bind overlapping surfaces on eIF4E and thus form mutually exclusive complexes. The multiple arrows between the RNMT and RNA export complexes indicate that there could be other complexes between the capping and export ones depicted. Not all eIF4E complexes known are shown here for simplicity.

Article Snippet: Antibodies used in Western blots Primary antibodies mouse RNMT (RNMT 3H31D12, Santa Cruz Biotechnology, Catalog No. sc517112) and mouse eIF4E (BD Biosciences, 610269), rabbit polyclonal RNMT (ProteinTech, 13743-1-AP), rabbit monoclonal 4E-BP1 (53H11, Cell Signaling Technology, #9644), rabbit polyclonal 4E-BP2, Cell Signaling Technology #2845, rabbit polyclonal RAM (FAM103A1 Polyclonal antibody, ProteinTech, 19422-1-AP) and GST Goat Polyclonal (Cytiva; catalog no. 45- 001-369).

Techniques: Western Blot, Binding Assay