Figure 4.
Figure 4. Structure of the β3 PSI domain. (A) Two different views of the superposition of the bent (PDB 3FCS), intermediate, and extended β3 structures on the PSI domain. Disulfide bonds, Pro33, and Leu33 are sticks. Selected cysteines are shown as Cα spheres. (B) Sequence alignment of a portion of the PSI domain containing the C26-C38 loop. Disulfide linkages are indicated. (C) Mn2+-stimulated binding of the ligand mimetic mAb PAC-1 to HEK293FT cells transfected with the indicated αIIb and β3 constructs. PAC-1 binding was performed in the presence of 1 mM of Ca2+/Mg2+ or 0.2 mM of Ca2+ plus 2 mM Mn2+. (D) Talin head (TH)–induced PAC-1 binding to HEK293FT cells transfected with the indicated αIIb and β3 constructs plus EGFP or EGFP-TH. PAC-1 binding was performed in the presence of 1 mM of Ca2+/Mg2+. (E) Mn2+-stimulated binding of fibronectin (Fn) to HEK293FT cells transfected with the indicated αV and β3 constructs. Fn binding was performed in the presence of 1 mM of Ca2+/Mg2+ or 0.2 mM of Ca2+ plus 2 mM of Mn2+. All the ligand binding results are presented as the mean fluorescence intensity (MFI) normalized to integrin expression. WT, wild type.

Structure of the β3PSI domain. (A) Two different views of the superposition of the bent (PDB 3FCS), intermediate, and extended β3 structures on the PSI domain. Disulfide bonds, Pro33, and Leu33 are sticks. Selected cysteines are shown as Cα spheres. (B) Sequence alignment of a portion of the PSI domain containing the C26-C38 loop. Disulfide linkages are indicated. (C) Mn2+-stimulated binding of the ligand mimetic mAb PAC-1 to HEK293FT cells transfected with the indicated αIIb and β3 constructs. PAC-1 binding was performed in the presence of 1 mM of Ca2+/Mg2+ or 0.2 mM of Ca2+ plus 2 mM Mn2+. (D) Talin head (TH)–induced PAC-1 binding to HEK293FT cells transfected with the indicated αIIb and β3 constructs plus EGFP or EGFP-TH. PAC-1 binding was performed in the presence of 1 mM of Ca2+/Mg2+. (E) Mn2+-stimulated binding of fibronectin (Fn) to HEK293FT cells transfected with the indicated αV and β3 constructs. Fn binding was performed in the presence of 1 mM of Ca2+/Mg2+ or 0.2 mM of Ca2+ plus 2 mM of Mn2+. All the ligand binding results are presented as the mean fluorescence intensity (MFI) normalized to integrin expression. WT, wild type.

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