| 2002 |
Raptor forms a stoichiometric complex with mTOR; this association negatively regulates mTOR kinase activity under nutrient deprivation, while raptor is required for nutrient-stimulated signaling to S6K1, maintenance of cell size, and mTOR protein expression. |
Co-immunoprecipitation, mass spectrometry, RNAi knockdown, cell size measurements |
Cell |
High |
12150925 12150926
|
| 2002 |
Raptor binds 4EBP1 and p70S6K and is required as a scaffold for mTOR-catalyzed phosphorylation of 4EBP1 in vitro; partial RNAi knockdown of raptor reduces mTOR-catalyzed 4EBP1 phosphorylation, and C. elegans raptor RNAi phenocopies Ce-TOR inactivation. |
In vitro kinase assay, Co-immunoprecipitation, RNAi in mammalian cells and C. elegans |
Cell |
High |
12150926
|
| 2003 |
Raptor binds the TOS (TOR signaling) motif of p70S6K and 4EBP1; a point mutation in the 4EBP1 TOS motif abolishes raptor binding and eliminates mTOR-catalyzed 4EBP1 phosphorylation in vitro and in vivo, demonstrating raptor as the substrate-recruiting scaffold. |
Co-immunoprecipitation, site-directed mutagenesis, in vitro kinase assay, cell size measurement |
The Journal of biological chemistry |
High |
12604610 12747827
|
| 2003 |
GbetaL (mLST8) binds the mTOR kinase domain and stabilizes the raptor–mTOR interaction; GbetaL stimulates mTOR kinase activity toward S6K1 and 4E-BP1, an effect reversed by stable raptor–mTOR association; nutrients and rapamycin regulate mTOR–raptor association only in complexes also containing GbetaL. |
Co-immunoprecipitation, in vitro kinase assay, RNAi, cell size measurement |
Molecular cell |
High |
12718876
|
| 2004 |
Rictor defines a second mTOR complex (mTORC2) that does not contain raptor and is rapamycin-insensitive; raptor-containing mTORC1 regulates S6K1 while rictor-containing mTORC2 modulates PKCα phosphorylation and the actin cytoskeleton. |
Co-immunoprecipitation, mass spectrometry, RNAi, immunofluorescence |
Current biology : CB |
High |
15268862
|
| 2004 |
Rapamycin/FKBP12 complex inhibits mTOR function at least in part by dissociating raptor from mTOR both in vivo and directly in vitro; this dissociation uncouples mTOR from raptor-dependent substrates without altering intrinsic mTOR catalytic activity. |
Co-immunoprecipitation, in vitro binding assay, in vitro kinase assay |
Genes to cells : devoted to molecular & cellular mechanisms |
High |
15066126
|
| 2005 |
The raptor–mTOR complex selectively phosphorylates rapamycin-sensitive forms of S6K1, while the rictor–mTOR complex phosphorylates rapamycin-resistant S6K1 mutants lacking the C-terminal domain; TOS motif-independent recognition is required for rictor-mTOR-mediated phosphorylation. |
In vitro kinase assay, Co-immunoprecipitation, mutant S6K1 constructs |
The Journal of biological chemistry |
High |
15809305
|
| 2005 |
Redox state regulates the raptor–mTOR complex: oxidizing agents increase S6K1 phosphorylation and make it nutrient-insensitive, while the reducing agent BAL stabilizes mTOR–raptor interaction (mimicking nutrient deprivation) and inhibits S6K1 phosphorylation. |
Co-immunoprecipitation, immunoblot, pharmacological redox manipulation |
The Journal of biological chemistry |
Medium |
16183647
|
| 2006 |
Raptor-dependent mTOR directly phosphorylates IRS-1 at Ser636/639; raptor binds IRS-1 directly and serves as a scaffold for this phosphorylation, providing a mechanism for mTOR-mediated negative feedback on PI3K/Akt signaling. |
Co-immunoprecipitation, RNAi knockdown, phospho-specific immunoblot, in vitro kinase assay |
Molecular and cellular biology |
High |
16354680 19561084
|
| 2006 |
Raptor is ubiquitinated by the DDB1-CUL4 ubiquitin ligase complex; the deubiquitylase UCH-L1 disrupts this DDB1-CUL4–raptor complex, counteracts raptor ubiquitination, and leads to mTORC1 dissolution with secondary mTORC2 increase. |
Co-immunoprecipitation, ubiquitination assay, shRNA knockdown, Uchl1 transgenic and knockout mice |
Molecular and cellular biology |
High |
23297343
|
| 2006 |
Mice lacking raptor die early in embryonic development, establishing that mTORC1/raptor function is essential for early development; mLST8 is required only for mTORC2 (rictor-mTOR) signaling to Akt and PKCα, not for raptor-mTOR signaling to S6K1. |
Conditional gene knockout mice, immunoprecipitation, immunoblot |
Developmental cell |
High |
17141160
|
| 2007 |
Electron microscopy reconstruction revealed that yeast TOR1 N-terminal HEAT repeats form a curved tubular domain that associates with the C-terminal WD40 domain of KOG1/Raptor; the N terminus of KOG1 is proximal to the TOR kinase domain, supporting a substrate-delivery model. |
Single-particle electron microscopy, 3D reconstruction at 25 Å resolution |
Molecular cell |
Medium |
17679098
|
| 2008 |
AMPK directly phosphorylates raptor on Ser722 and Ser792 under energy stress; this phosphorylation induces 14-3-3 binding to raptor and is required for mTORC1 inhibition and cell-cycle arrest induced by energy stress. |
In vitro kinase assay, phospho-specific antibodies, Co-immunoprecipitation of 14-3-3, RNAi, phospho-mutant rescue experiments |
Molecular cell |
High |
18439900
|
| 2008 |
The Rag GTPases interact with mTORC1 in an amino-acid-sensitive manner through raptor; GTP-loaded Rag promotes mTORC1 lysosomal/intracellular relocalization to activate mTOR without directly stimulating mTOR kinase activity. |
Co-immunoprecipitation, dominant-active/dominant-negative Rag constructs, immunofluorescence localization, RNAi |
Science (New York, N.Y.) |
High |
18497260
|
| 2008 |
RSK1/2, activated by the Ras/MAPK pathway, directly phosphorylate raptor on conserved RXRXXpS/T motifs in an evolutionarily conserved region; raptor phosphorylation-deficient mutants show reduced mTOR kinase activity, linking MAPK pathway to mTORC1 activation. |
In vitro kinase assay, RNAi, quantitative mass spectrometry, site-directed mutagenesis, oncogenic Ras/MEK constructs |
Current biology : CB |
High |
18722121
|
| 2008 |
mTOR–raptor complex phosphorylates SGK1 at S422; raptor shRNA impairs mTOR-driven SGK1 activation (but not Akt), and mTOR/raptor/SGK1 complexes are detected in cells, implicating SGK1 as a direct mTORC1 substrate that mediates cytoplasmic p27 mislocalization. |
In vitro kinase assay, Co-immunoprecipitation, shRNA knockdown, phospho-specific immunoblot |
Molecular cell |
High |
18570873
|
| 2008 |
Raptor is required for Akt-induced NF-κB activation downstream of mTOR; mTOR–raptor complex interacts with and stimulates IKK; rapamycin suppresses IKK activity possibly via raptor–mTOR dissociation. |
RNAi knockdown, Co-immunoprecipitation, IKK kinase assay, pharmacological inhibition |
Genes & development |
Medium |
18519641
|
| 2008 |
FKBP12 deficiency in mouse brain increases basal mTOR phosphorylation and mTOR–Raptor interactions along with enhanced S6K phosphorylation, demonstrating that FKBP12 normally restrains mTOR–Raptor complex assembly. |
Brain-specific Fkbp12 conditional knockout mice, Co-immunoprecipitation, immunoblot |
Neuron |
Medium |
19081378
|
| 2009 |
Raptor binds the SAIN domain of IRS-1 and this interaction is required for mTOR-mediated phosphorylation of IRS-1 at Ser-636/639; IRS-1 lacking the SAIN domain does not interact with raptor, is not phosphorylated at these sites, and has enhanced PI3K association. |
Co-immunoprecipitation, deletion mutant constructs, RNAi, phospho-specific immunoblot |
The Journal of biological chemistry |
Medium |
19561084
|
| 2009 |
Raptor Ser863 is phosphorylated in response to insulin via the canonical PI3K/TSC/Rheb/mTORC1 pathway in a rapamycin-sensitive manner; Ser863 phosphorylation is a hierarchical master switch required for phosphorylation at Ser859 and Ser855; multisite phosphorylation-deficient raptor shows reduced in vitro mTORC1 kinase activity toward 4EBP1. |
Tandem mass spectrometry, phospho-specific antibody generation, site-directed mutagenesis, in vitro kinase assay, Rheb overexpression |
The Journal of biological chemistry |
High |
19864431
|
| 2009 |
Hsp90 co-immunoprecipitates with raptor; geldanamycin disrupts Hsp90–raptor association (without affecting raptor–mTOR binding) and suppresses mTOR-mediated phosphorylation of S6K and 4E-BP1, indicating Hsp90 facilitates mTOR/raptor complex activity through raptor binding. |
Co-immunoprecipitation, pharmacological inhibition, immunoblot |
Journal of biochemistry |
Medium |
16428328 19586661
|
| 2010 |
ERK1/2 interact with raptor and directly phosphorylate it on Ser8, Ser696, and Ser863 in response to Ras/MAPK activation; phosphorylation-deficient raptor alleles reduce mTORC1 activity and 4E-BP1 phosphorylation. |
Co-immunoprecipitation, in vitro kinase assay, mass spectrometry, phospho-specific antibodies, site-directed mutagenesis |
The Journal of biological chemistry |
High |
21071439
|
| 2010 |
CDC2/CDK1 (cdc2) phosphorylates raptor on Ser696 and Thr706 during mitosis; Cyclin B co-immunoprecipitates with raptor in mitotic cells, and these mitotic phosphorylation events regulate mTORC1 during cell division. |
Tandem mass spectrometry, phospho-specific antibodies, site-directed mutagenesis, Co-immunoprecipitation, cell synchronization |
PloS one |
High |
20169205
|
| 2010 |
Mitotic phosphorylation of raptor (by CDK1 and GSK3 pathways) facilitates G2/M cell cycle transit; phosphorylation-deficient raptor mutants cause G2/M delay while raptor depletion causes G1 accumulation; mitotic raptor promotes IRES-dependent mRNA translation. |
Phosphopeptide mapping, site-directed mutagenesis, cell cycle analysis, dominant-negative/constitutive kinase constructs |
Molecular and cellular biology |
Medium |
20439490
|
| 2011 |
ULK1 phosphorylates raptor at multiple sites in vivo and in vitro (prominently Ser855 and Ser859, with moderate Ser792); ULK1-mediated raptor phosphorylation reduces the ability of raptor to bind substrate 4E-BP1 without disrupting mTORC1 complex integrity, providing a negative feedback mechanism. |
In vitro kinase assay, phospho-specific antibodies, Co-immunoprecipitation, shRNA knockdown, overexpression |
Autophagy |
High |
21460630
|
| 2011 |
Raptor and Rheb negatively regulate skeletal myogenic differentiation through suppression of IRS1; raptor or Rheb knockdown enhances C2C12 differentiation accompanied by increased Akt activation and elevated IRS1 levels, and IRS1 knockdown abolishes this enhancement. |
RNAi knockdown, overexpression, C2C12 differentiation assay, immunoblot epistasis |
The Journal of biological chemistry |
Medium |
21852229
|
| 2012 |
ICK (intestinal cell kinase) phosphorylates raptor at Thr908 both in vitro and in vivo; Raptor T908A mutant markedly impairs mTORC1 activation by insulin or Rheb overexpression without disrupting mTORC1 complex integrity. |
In vitro kinase assay, mass spectrometry, phospho-specific antibody, site-directed mutagenesis, Co-immunoprecipitation |
The Journal of biological chemistry |
High |
22356909
|
| 2013 |
FLIM-FRET in live cells confirmed direct physical interaction between mTOR and raptor in the cytoplasm and nucleus; amino acid withdrawal and re-addition (but not rapamycin) alter mTOR intracellular distribution. |
FRET-FLIM live-cell imaging, GFP/DsRed fusion proteins |
BMC cell biology |
Medium |
23311891
|
| 2015 |
GSK3 phosphorylates raptor at Ser859; GSK3 inhibition or shRNA silencing reduces mTOR–raptor interaction and attenuates amino-acid-regulated mTORC1 signaling, increased autophagic flux, and reduced proliferation. |
Pharmacological inhibition, shRNA, phospho-specific antibody, Co-immunoprecipitation, site-directed mutagenesis (S859A) |
The Biochemical journal |
Medium |
26348909
|
| 2015 |
Glucose starvation in budding yeast triggers Snf1/AMPK-dependent phosphorylation of Kog1/Raptor at Ser491/494, driving TORC1 disassembly and condensation of Kog1 into a single body near the vacuole; these bodies increase the TORC1 activation threshold (hysteresis) during prolonged starvation. |
Yeast genetics, live-cell fluorescence microscopy, phospho-mutant constructs, TORC1 activity assays |
eLife |
High |
26439012
|
| 2015 |
NLK phosphorylates raptor on Ser863 in response to osmotic/oxidative stress; this phosphorylation disrupts raptor's interaction with Rag GTPases, inhibits mTORC1 lysosomal localization, and suppresses mTORC1 activation; Raptor S863A knock-in cells are defective in stress-induced mTORC1 inhibition. |
In vitro kinase assay, Co-immunoprecipitation, phospho-specific antibody, Nlk knockout and Raptor knock-in cells, immunofluorescence |
Genes & development |
High |
26588989
|
| 2016 |
Free (mTORC1-independent) Raptor negatively regulates hepatic Akt activity and lipogenesis by stabilizing the Akt phosphatase PHLPP2, reducing its β-TrCP-mediated degradation; this reveals a scaffolding function of Raptor independent of mTOR kinase. |
Hepatocyte-specific Raptor knockout mice, overexpression constructs, Co-immunoprecipitation, immunoblot, liver lipid measurements |
Nature communications |
Medium |
26743335
|
| 2017 |
The mTOR–Raptor–S6K1 axis regulates Runx2 expression through S6K1-mediated phosphorylation of estrogen receptor α, which binds DLX5 and augments Runx2 enhancer activity; heterozygous Raptor mutation in osteoblasts aggravates bone defects in Runx2+/− mice. |
Conditional knockout mice, immunoblot, chromatin immunoprecipitation, genetic epistasis (Raptor×Runx2 double mutant) |
Cell death and differentiation |
Medium |
28686577
|
| 2017 |
USP9X deubiquitylase physically associates with Raptor in embryonic brains, opposes proteasomal degradation of Raptor, and thereby maintains Raptor protein levels and mTORC1 signaling in neural progenitors; loss of Usp9x phenocopies Raptor-null neurospheres in reducing mTORC1 activity. |
Co-immunoprecipitation from embryonic brain, USP9X loss- and gain-of-function in cultured cells and Nestin-Cre Usp9x mice, proteasome inhibition assay, EdU proliferation assay |
Scientific reports |
Medium |
28341829
|
| 2019 |
PKA phosphorylates Raptor at Ser791 in response to Gαs-coupled GPCR activation, leading to decreased mTORC1 activity; Raptor S791A mutant partially rescues mTORC1 activity after PKA activation, and this pathway operates in multiple cell lines and mouse tissues. |
In vitro kinase assay, phospho-specific antibody, Raptor S791A site-directed mutagenesis, pharmacological GPCR agonists, immunoblot in mouse tissues |
eLife |
High |
31112131
|
| 2019 |
SHOC2 (a RAS activator) competes with mTOR for Raptor binding; SHOC2–Raptor interaction inhibits mTORC1 and induces autophagy, while Raptor binding to SHOC2 blocks RAS-MAPK signaling; FBXW7-mediated ubiquitination of SHOC2 terminates this cross-talk. |
Co-immunoprecipitation, competitive binding assay, ubiquitination assay, autophagy flux assay, cell proliferation assay |
Cell reports |
Medium |
30865892
|
| 2019 |
TBK1 phosphorylates Raptor at Ser877 in vitro and promotes Ser877 phosphorylation in cells in response to pathogen-associated molecules; phosphorylation at Ser877 inversely correlates with mTORC1 activity, and Raptor S877A mutant increases mTORC1 activity. |
In vitro kinase assay coupled with mass spectrometry, phospho-specific antibody, Raptor S877A site-directed mutagenesis, immunoblot |
Scientific reports |
Medium |
31530866
|
| 2020 |
Leucine regulates autophagy via its metabolite acetyl-CoA: AcCoA promotes EP300-dependent acetylation of raptor, which activates mTORC1 and suppresses autophagy; leucine deprivation decreases raptor acetylation and causes mTORC1 inhibition predominantly through this mechanism. |
Pharmacological manipulation of AcCoA, EP300 inhibitor, Co-immunoprecipitation, raptor acetylation assay, autophagy flux assay in multiple cell lines and neurons |
Nature communications |
High |
32561715
|
| 2020 |
Hepatic peroxisomal β-oxidation suppresses lipophagy via RPTOR acetylation and mTOR activation; ACOX1 deficiency decreases cytosolic acetyl-CoA, reduces RPTOR acetylation, inhibits mTORC1, and induces lipophagy. |
Liver-specific Acox1 knockout mice, acetylation assay, mTORC1 activity measurement, lipophagy quantification |
Autophagy |
Medium |
32687428
|
| 2020 |
AMPK-mediated phosphorylation of both RAPTOR (Ser722/Ser792) and TSC2 is required for full mTORC1 inhibition by metformin in primary hepatocytes and intact liver; Raptor knock-in mice (S722A/S792A) show incomplete mTORC1 inhibition and an attenuated transcriptional response to metformin. |
Raptor Ser722A/Ser792A knock-in mice, primary hepatocyte cultures, immunoblot, RNA-seq |
Genes & development |
High |
32912901
|
| 2021 |
VHL interacts with RAPTOR and promotes RAPTOR degradation through ubiquitination, thereby suppressing mTORC1 signaling; loss of VHL in ccRCC increases RAPTOR levels and mTORC1 hyperactivation, consistent with a conserved mechanism also observed in C. elegans vhl-1 mutants. |
Co-immunoprecipitation, ubiquitination assay, VHL overexpression/silencing, C. elegans vhl-1 genetic analysis, immunoblot |
Scientific reports |
Medium |
34290272
|
| 2023 |
O-GlcNAcylation of Raptor at Thr700 by OGT (driven by glucose availability) facilitates Raptor–Rag GTPase interactions and promotes lysosomal translocation of mTOR, thereby activating mTORC1; AMPK-mediated phosphorylation of Raptor suppresses Raptor O-GlcNAcylation and inhibits Raptor–Rag interactions. |
O-GlcNAc proteomics, site-directed mutagenesis (T700A), Co-immunoprecipitation, lysosomal fractionation, immunofluorescence, OGT inhibition |
Molecular cell |
High |
37541260
|