mTOR Signaling Pathway


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Western blot analysis of whole cell lysates probed with Rabbit Anti-mTOR Antibody (VPA00174) followed by detection with HRP conjugated Goat Anti-Rabbit IgG (1/10,000, STAR208P) and visualized on the ChemiDoc MP with 2 second exposure.

Western blot analysis of whole cell lysates probed with Rabbit Anti-mTOR Antibody (VPA00174) followed by detection with HRP conjugated Goat Anti-Rabbit IgG (1/10,000, STAR208P) and visualized on the ChemiDoc MP with 2 second exposure.

The mammalian target of rapamycin (mTOR) is a serine/threonine kinase, which forms the core component of mTOR complex 1 (mTORC1) and mTOR complex 2 (mTORC2) (Bhat et al. 2015) (Figure 1). The complexes differ structurally and functionally and have different sensitivity to the macrolide rapamycin.

mTORC1 regulates protein synthesis, lipid synthesis, autophagy and metabolic programmes (Bhat et al. 2015 and Laplante and Sabatini 2012) and can be activated by various stimuli such as growth factors, nutrients, energy and stress signals (Populo et al. 2012). The mTORC1 complex consists of  mTOR, DEP domain-containing mTOR-interacting protein (Deptor), mammalian lethal with SEC13 protein 8 (mLST8), proline-rich AKT1 substrate 1 (PRAS40) and regulatory-associated protein of mTOR (Raptor) (Figure 1). Deptor binding to mTOR negatively regulates its kinase activity (Varusai and Nguyen 2018). mLST8 binding to the mTOR kinase domain stabilizes the Raptor-mTOR interaction (Kim et al. 2003). PRAS40 regulates mTORC1 kinase activity as a direct inhibitor of substrate binding (Wang et al. 2007). Raptor binding mediates mTOR’s function as a scaffold in the mTOR-signaling cascade and binds directly to mTOR (Hara et al. 2002).

The mTOR2 complex regulates cell survival and cytoskeletal organization (Oh and Jacinto 2011) and can be activated by growth factor binding. The complex consists of mTOR, Deptor, mLST8, rapamycin-insensitive companion of mTOR (Rictor), stress-activated protein kinase-interacting protein 1 (mSIN1) and protein observed with Rictor (Protor) (Populo et al. 2012) (Figure 1). Rictor is a key component of the mTORC2 complex and is overexpressed in various cancer types associated with poor survival chances (El Shamieh et al. 2018). The Rictor and mTOR kinases both phosphorylate AKT at serine 473 (Hresko and Mueckler 2005; Sarbassov et al. 2005) as well as facilitate PDK1 mediated phosphorylation at AKT threonine residue 308 (Sarbassov et al. 2005). In addition, mSin1 has also been reported to play a role in mTORC2's capacity to phosphorylate AKT (Frias et al. 2006). Protor is a Rictor-binding subunit of mTORC2 (Pearce at al. 2007) and is required for SGK1 activation in the kidney (Pearce et al. 2011).

Fig. 1. Schematic drawing of the mTORC1 and mTORC2 complexes.

Fig. 1. Schematic drawing of the mTORC1 and mTORC2 complexes. The mTORC1 complex consists of mTOR, Deptor, mLST8, PRAS40 and Raptor while the mTORC2 contains mTOR, Deptor, mLST8, Rictor, mSIN1 and Protor (Populo et al. 2012).

mTOR plays a role in various physiological processes; more detailed information about the importance of the complex in the regulation of protein synthesis can be found here. One key role for mTOR is that of a negative regulator of autophagy (Mizushima et al. 2008). mTORC1 regulates this process by phosphorylation  and suppression of the ULK-Atg13-FIP200 kinase complex, which is an essential mediator of autophagy. Inhibition of mTORC1 leads to autophagosome formation, which subsequently fuse with lysosomes (Jung et al. 2009; Laplante and Sabatini 2012). The death-associated protein 1 (DAP1) is also an mTOR substrate that negatively regulates autophagy (Koren et al. 2010).

Inhibition of mTORC1 kinase activity causes reduction in DAP1 phosphorylation, and converts the protein into an active suppressor of autophagy (Koren et al. 2010).

Fig. 2. The role of the mTORC1 complex in the regulation of autophagy

Fig. 2. The role of the mTORC1 complex in the regulation of autophagy. mTORC1 directly phosphorylates and inhibits the ULK-Atg13-FIP200 complex when nutrients are abundant. Phosphorylation of ULK1 and ATG13 prevents induction of autophagy. Upon starvation or rapamycin treatment, mTOR1C is inhibited, which enables the induction of autophagy (Jung et al 2009; Laplante and Sabatini 2012). 

Mutations in the mTOR signaling pathway as well as aberrant mTOR signaling have been associated with the development of many diseases including cancer (Populo et al. 2012). Therefore, mTOR represents an attractive therapeutic target (Bhat et al. 2015), which is why many mTOR inhibitors are currently being tested in clinical trials.

Our mTOR Antibody Range

    DescriptionSpecificityTargetFormatHostIsotypeClone Applications Citations Product Type Code


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    • El Shamieh S (2018). RICTOR gene amplification is correlated with metastasis and therapeutic resistance in triple-negative breast cancer. Pharmacogenomics 19, 757-760.
    • Frias MA et al. (2006). mSin1 is necessary for Akt/PKB phosphorylation, and its isoforms define three distinct mTORC2s. Curr Biol 16, 1865-70.
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    • Jung CH et al. (2009). ULK-Atg13-FIP200 complexes mediate mTOR signaling to the autophagy machinery. Mol Biol Cell 20, 1992-2003.
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    • Koren I et al. (2010). DAP1, a novel substrate of mTOR, negatively regulates autophagy. Curr Biol 20, 1093-8.
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    • Pearce LR et al. (2007). Identification of Protor as a novel Rictor-binding component of mTOR complex-2. Biochem J 405, 513-22.
    • Pearce LR et al. (2011). Protor-1 is required for efficient mTORC2-mediated activation of SGK1 in the kidney. Biochem J 436, 169-79.
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    • Sarbassov DD et al. (2005). Phosphorylation and regulation of Akt/PKB by the rictor-mTOR complex. Science 307(5712), 1098-101.
    • Varusai TM and Nguyen LK (2018). Dynamic modelling of the mTOR signalling network reveals complex emergent behaviours conferred by DEPTOR. Sci Rep 12, 8(1):643.
    • Wang L et al. (2007). PRAS40 regulates mTORC1 kinase activity by functioning as a direct inhibitor of substrate binding. J Biol Chem 282, 20036-44.