Figure 3
Figure 3. Multiprotein complexes involving CMS, CIN85, and CD2BP3 can be recruited to the cytoplasmic domain of human pTα. Total lysates from COS7 cells transfected with the indicated amounts of CD2BP3-Flag (A) or CMS-Flag and CD2BP3-Flag (B) were subjected to pull-down with GST-pTα. Precipitated proteins were analyzed by Western blotting with an anti-Flag mAb. COS7 cells were transiently cotransfected with the indicated amounts of CD2BP3-Flag and CIN85-HA (C) or CD2BP3-Flag, CMS-Flag, and CIN85-HA (D). Total-cell lysates and proteins precipitated with GST-pTα were analyzed by immunoblotting using either an anti-Flag mAb to detect CD2BP3 and CMS (top 2 panels) or an anti-HA mAb to detect CIN85 (bottom 2 panels). *Nonspecific band recognized by the anti-HA antibody. Data are representative of at least 3 independent experiments. Vertical lines have been inserted to indicate a repositioned gel lane.

Multiprotein complexes involving CMS, CIN85, and CD2BP3 can be recruited to the cytoplasmic domain of human pTα. Total lysates from COS7 cells transfected with the indicated amounts of CD2BP3-Flag (A) or CMS-Flag and CD2BP3-Flag (B) were subjected to pull-down with GST-pTα. Precipitated proteins were analyzed by Western blotting with an anti-Flag mAb. COS7 cells were transiently cotransfected with the indicated amounts of CD2BP3-Flag and CIN85-HA (C) or CD2BP3-Flag, CMS-Flag, and CIN85-HA (D). Total-cell lysates and proteins precipitated with GST-pTα were analyzed by immunoblotting using either an anti-Flag mAb to detect CD2BP3 and CMS (top 2 panels) or an anti-HA mAb to detect CIN85 (bottom 2 panels). *Nonspecific band recognized by the anti-HA antibody. Data are representative of at least 3 independent experiments. Vertical lines have been inserted to indicate a repositioned gel lane.

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