Architecture of human mTOR complex 1
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From sensing leucine to metabolic control The mTORC1 protein kinase complex plays central roles in regulating cell growth and metabolism and is implicated in common human diseases such as diabetes and cancer. The level of the amino acid leucine tells an organism a lot about its physiological state, including how much food is available, how much insulin is going to be needed, and whether new muscle mass can be made (see the Perspective by Buel and Blenis). Wolfson et al. identified a biochemical sensor of leucine, Sestrin2, which connects the concentration of leucine to the control of organismal metabolism and growth. When leucine bound to Sestrin2, it was released from a complex with the mTORC1 regulatory factor GATOR2, activating the mTORC1 complex. Saxton et al. describe the crystal structure of Sestrin2 and show how it specifically detects leucine. Aylett et al. determined the structure of human mTORC1 by cryoelectron microscopy and the crystal structure of a regulatory subunit, Raptor. The results reveal the structural basis for the function and intricate regulation of this important enzyme, which is also a strategic drug target. Science , this issue p. 43 , p. 48 , p. 53 ; see also p. 25
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Both mTOR complexes control cell growth and metabolism in response to the availability of nutrients, energy, and growth factors.
“Both complexes control cell growth and metabolism in response to the availability of nutrients, energy, and growth factors.”
From Metformin, the Aspirin of the 21st Century: Its Role in Gestational Diabetes Mellitus, Prevention of Preeclampsia and Cancer, and the Promotion of Longevity (2017) · cites this paper as [237]
Rapamycin acts by interacting with a family of TOR molecules that is highly-conserved functionally and evolutionarily from yeast to humans, and it contains two multiprotein complexes that are functionally and structurally different: mTORC1 is rapamycin-sensitive; mTORC2 is rapamycin-resistant.
“Rapamycin acts by interacting with a family of TOR molecules that is highly-conserved functionally and evolutionarily from yeast to humans, and it contains two multiprotein complexes that are functionally and structurally different: the first, mTORC1, is rapamycin-sensitive; and the second, mTORC2, is rapamycin-resistant(237).”
From Metformin, the Aspirin of the 21st Century: Its Role in Gestational Diabetes Mellitus, Prevention of Preeclampsia and Cancer, and the Promotion of Longevity (2017) · cites this paper as [237]
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References 57 · Cited by 344
- Authors
- Aylett, C. H. S., Sauer, E., Imseng, S., Boehringer, D., Hall, M. N., Ban, N., & Maier, T.
- Affiliations
- ETH Zurich (CH)
- University of Basel (CH)
- Corresponding author
- Aylett, Christopher H. S.
- Sauer, Evelyn
- Imseng, Stefan
- Hall, Michael N.
- Ban, Nenad
- Maier, Timm
- ORCID
- Venue
- Science
- Published
- 2016-01
- Volume
- 351
- Issue
- 6268
- Pages
- 48-52
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W2207318443
- Cited by
- 344
- References
- 57
- Citations by year
- 2026: 13 · 2025: 18 · 2024: 25 · 2023: 33 · 2022: 25 · 2021: 34 · 2020: 37 · 2019: 47 · 2018: 37 · 2017: 41 · 2016: 33 · 2015: 1
- FWCI
- 16.34
- Type
- journal article
- Language
- en
- Open access
- green
- doi.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- edoc (University of Basel) (acceptedVersion)
- DORA PSI (Paul Scherrer Institute) (submittedVersion)
- edoc (University of Basel)
- Funders
- REA (328159)
- European Research Council
- Swiss National Science Foundation
- National Centre of Excellence in RNA and Disease (138262, 145023)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › PI3K/AKT/mTOR signaling in cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
- Keywords
- mTORC1, Sestrin2, leucine sensing, GATOR2, raptors, amino acid signaling, cell growth regulation, metabolic control, therapeutic target
- MeSH terms
- Mechanistic Target of Rapamycin Complex 1, Regulatory-Associated Protein of mTOR, Mechanistic Target of Rapamycin Complex 2, mTOR Associated Protein, LST8 Homolog, Humans, Protein Binding, Substrate Specificity, Protein Structure, Secondary, Protein Structure, Tertiary, Catalytic Domain, Cryoelectron Microscopy, Tacrolimus Binding Proteins, Multiprotein Complexes, Adaptor Proteins, Signal Transducing, Protein Multimerization, TOR Serine-Threonine Kinases
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