Several different assays can be used by scientists to measure metabolism in a variety of contexts. These include methods to directly determine metabolic rates as well as to examine key signaling pathways and environmental cues, like hypoxia and oxidative stress, which directly influence metabolism under normal and pathological conditions.
Hypoxia and oxidative stress are both a cause and consequence of alterations in cellular metabolism. Cell Signaling Technology is proud to offer antibodies to investigate key biomarkers of hypoxia and oxidative stress. Available products can be accessed directly from the CST Hypoxia Interactive Signaling Pathway.
Mitochondria are cellular organelles that serve the primary energy factories to support cellular function. The conversion of metabolites from the TCA cycle into ATP is achieved by the transfer of electrons from these intermediates through the respiratory chain on the mitochondrial inner membrane. Assays to examine mitochondrial respiration provide a direct readout of cellular metabolic activity.
Mitochondrial integrity is essential for the regulation of cellular energy the regulation of apoptosis.
Amino acids are the building blocks of cellular proteins and also serve as key nutrients to fuel cellular processes. For example, Glutamine is an important metabolic fuel that helps rapidly proliferating cells meet their demands for ATP. Direct links to CST products available to study amino acid metabolism, including key enzymes like GLS, IDH1, and IDH2 are accessible via the CST Glutamine Metabolism Interactive Pathway.
The mechanistic target of rapamycin (mTOR) is a serine threonine kinase that serves a master regulator of cell growth and metabolism. mTOR integrates signaling from extracellular growth factors, cytokines, and acts as a nutrient sensor to affect multiple cellular processes, including cell proliferation, survival, cell growth and protein translation. mTOR exists in two distinct signaling complexes, termed mTORC1 and mTORC2, that receive signaling inputs primarily via the PI3K/AKT, ERK1/2, and AMPK pathways. Key downstream targets of mTORC1 include p70/S6K and 4E-BP1/2, while mTORC2 transduces signals via SGK1, PKCa, and AKT. Components of mTOR signaling can be queried using reagents from the CST mTOR substrate sampler kit which includes:
Serine/Threonine Kinase |
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Downstream effector of mTORC1, Thr389 correlates with kinase activity |
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Downstream effector of mTORC1, Ser371 correlates with kinase activity |
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Downstream effector of mTORC1, inhibits cap-dependent translation,Thr37/46 are readouts of mTOR activity |
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mTOR Ser2448 is phosphorylated via PI3K/AKT activation |
AMP-activated protein kinase (AMPK) is master regulator of cellular energy homeostasis that modulates both glucose and lipid metabolism. AMPK phosphorylates downstream targets to regulate glucose metabolism (e.g. PFKFB3, GYS1), lipid metabolism (e.g. HMGR, ACC1, PLD1), transcription (e.g. (HDAC4/5/7, p300, Srebp1), and cell growth/autophagy (e.g. Raptor, ULK1, Becilin-1). Components of AMPK signaling can be queried using reagents from the CST AMPK substrate sampler kit which includes:
Serine/Threonine Kinase |
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Serine/Threonine Kinase, phosphorylation at Thr172 is essential for activation |
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Serine/Threonine Kinase and downstream effector of AMPK linked to autophagy |
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Phosphorylation of ULK1 by AMPK at Ser555 is critical for starvation-induced autophagy, cell survival under conditions of low nutrients and energy, and mitochondiral homeostasis |
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AMPK substrate and component of mTORC1 |
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Ser 792 is phosphorylated by AMPK to inhibit mTORC1 |
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Downstream effector of AMPK linked to autophagy |
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Ser 93 (in humans) is phosphorylated by AMPK induce autophagy. Corresponds to murine Ser 91 |
The Warburg Effect is a metabolic adaptation of many cancers that promotes cancer cell growth and survival. Specifically, cancer cells tend to favor metabolism via glycolysis over the more efficient and commonly used oxidative phosphorylation pathway even in the presence of oxygen. Several signaling pathways including activation of the PI3K/AKT and RAS contribute to the Warburg effect. In addition, a dimeric form of the pyruvate kinase isoenzyme M2 (PKM2) is thought to play a central role in the Warburg effect. One hallmark of the Warburg effect is increased production of lactate. Key component contributing to the Warburg effect and products to assay their expression and activity can be directly access via the CST Warburg Effect Signaling Pathway.
Insulin, the major hormone controlling cellular energy functions such as glucose and lipid metabolism, acts by binding to and activating the insulin receptor tyrosine kinase. Receptor activation induces the recruitment of the IRS family of adaptor proteins and downstream activation predominantly through the PI3K/AKT and ERK1/2 pathways to affect numerous cellular processes. Components of insulin receptor signaling can be assayed using reagents in the CST Insulin Receptor Substrate Sampler Kit, which includes:
Insulin Receptor signaling adaptor protein |
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Ser 307 is phosphorylated by JNK and IKK |
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Ser 612 phosphorylation is mediated by the PKC an mTOR pathways |
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Downstream effector of mTORC1, inhibits cap-dependent translation,Thr37/46 are readouts of mTOR activity |
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Insulin Receptor signaling adaptor protein |
Several additional methods exist to measure the levels and activities of key metabolic processes in cells. These include:
Learn more about Metabolism.