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. 2021 Feb 4;184(3):655–674.e27. doi: 10.1016/j.cell.2020.12.024

Figure 1.

Figure 1

G3BP1 suppresses mTORC1 activation by insulin and nutrients

(A) Re-analysis of the MTOR interactome (Schwarz et al., 2015). Shown are mean log10 ratios of proteins in MTOR versus mock IP.

(B) IP against MTOR or mock (rat immunoglobulin G [IgG]). n = 6.

(C) Arsenite-treated shG3BP1 #1 cells. n = 4.

(D) Quantitation of G3BP1 in (C). Shown are data points and mean ± SEM.

(E) Quantitation of RPS6KB1-pT389 in (C). Data are shown as in (D).

(F) Insulin and amino acid (insulin/aa)-stimulated shG3BP1 #1 cells. n = 7.

(G) Quantitation of G3BP1 in (F). Shown are data points and mean ± SEM.

(H) Quantitation of RPS6KB1-pT389 in (F). Data are shown as in (G).

(I) Quantitation of RPS6-pS235/236 in (F). Data are shown as in (G).

(J) Insulin/aa-stimulated shG3BP1 #1 cells. n = 5.

(K) Quantitation of G3BP1 in (J). Shown are data points and mean ± SEM.

(L) Quantitation of RPS6KB1-pT389 in (J). Data are shown as in (K).

(M) Quantitation of RPS6-pS235/236 in (J). Data are shown as in (K).

(N) Insulin/aa-stimulated G3BP1 KO cells. n = 3.

(O) Quantitation of G3BP1 in (N). Shown are data points and mean ± SEM.

(P) Quantitation of RPS6KB1-pT389 in (N). Data are shown as in (O).

(Q) Quantitation of RPS6-pS235/236 in (N). Data are shown as in (O).

(R) Full-medium-cultured G3BP1 KO cells. n = 5.

(S) Quantitation of RPS6KB1-pT389 in (R). Shown are data points and mean ± SEM.

(T) Rapamycin treatment of insulin/aa-stimulated shG3BP1 #1 cells. n = 4.

(U) Quantitation of G3BP1 in (T). Shown are data points and mean ± SEM.

(V) Quantitation of RPS6KB1-pT389 in (T). Data are shown as in (U).

(W) Insulin/aa-stimulated G3BP1 KO cells transfected with MYC-FLAG-G3BP1 (48 h). n = 3.

(X) Quantitation of RPS6KB1-pT389 in (W). Shown are data points and mean ± SEM.

See also Figures S1 and S2 and Table S1.