#cysteine — Public Fediverse posts

Interesting ChemRxiv preprint by the group of Katrin Rittinger. They use enantiomeric pairs of covalent inhibitors to profile ligandable cysteines in the proteome. Interesting use of machine learning to predict new compounds that can add most to the ligandable space.

https://doi.org/10.26434/chemrxiv.15002030/v1

#ChemicalProbes #ChemicalProteomics #ProteoProbes #Chemistry #ChemBio #Ligandability #Cysteine #CovalentInhibitor

Interesting ChemRxiv preprint by the group of Katrin Rittinger. They use enantiomeric pairs of covalent inhibitors to profile ligandable cysteines in the proteome. Interesting use of machine learning to predict new compounds that can add most to the ligandable space.

https://doi.org/10.26434/chemrxiv.15002030/v1

#ChemicalProbes #ChemicalProteomics #ProteoProbes #Chemistry #ChemBio #Ligandability #Cysteine #CovalentInhibitor

Interesting ChemRxiv preprint by the group of Katrin Rittinger. They use enantiomeric pairs of covalent inhibitors to profile ligandable cysteines in the proteome. Interesting use of machine learning to predict new compounds that can add most to the ligandable space.

https://doi.org/10.26434/chemrxiv.15002030/v1

#ChemicalProbes #ChemicalProteomics #ProteoProbes #Chemistry #ChemBio #Ligandability #Cysteine #CovalentInhibitor

Interesting ChemRxiv preprint by the group of Katrin Rittinger. They use enantiomeric pairs of covalent inhibitors to profile ligandable cysteines in the proteome. Interesting use of machine learning to predict new compounds that can add most to the ligandable space.

https://doi.org/10.26434/chemrxiv.15002030/v1

#ChemicalProbes #ChemicalProteomics #ProteoProbes #Chemistry #ChemBio #Ligandability #Cysteine #CovalentInhibitor

Interesting ChemRxiv preprint by the group of Katrin Rittinger. They use enantiomeric pairs of covalent inhibitors to profile ligandable cysteines in the proteome. Interesting use of machine learning to predict new compounds that can add most to the ligandable space.

https://doi.org/10.26434/chemrxiv.15002030/v1

#ChemicalProbes #ChemicalProteomics #ProteoProbes #Chemistry #ChemBio #Ligandability #Cysteine #CovalentInhibitor

https://www.europesays.com/ie/452625/ Scientists identify STING switch driving inflammation in Alzheimer’s disease #Aging #Alzheimer'sDisease #Brain #Cell #Chronic #Cysteine #Éire #Health #IE #ImmuneSystem #inflammation #Ireland #Molecule #MouseModel #Nerve #Preclinical #Protein #Research

This popular supplement may increase risk of birth defects, study finds
news article, 27 March 2026
https://www.sciencedaily.com/releases/2026/03/260326075552.htm

"A new study reveals that high doses of antioxidants—often seen as harmless or beneficial—may actually impact future generations. "

The dose doesn't seem that high "127 mg/kg/day N-acetylcysteine (Figures 1B,C) and 0.013 mg/kg/day selenium ", that works out to a male human equivalent dose of ~ 929 mg NAC and 0.095 mg Se. The NAC + Se was given to mice orally in their water supply, with stevia added - which also has antioxidant properties.

To calculate the equivalent dose I divided the mouse dose by 12.3 and multiplied by the average male weight in the USA, 90 kg.
https://pmc.ncbi.nlm.nih.gov/articles/PMC4804402/#T1

~
I'm wondering if the mice have pheomelanin in their testes; some animals do:
https://onlinelibrary.wiley.com/doi/abs/10.1111/pcmr.12231

Pheomelanin regulates intracellular cysteine in male finches:
https://mastodon.social/@ScienceScholar/115872514267263073

#Supplements #NAC #cysteine #selenium #stevia #anitoxidants #health

This popular supplement may increase risk of birth defects, study finds
news article, 27 March 2026
https://www.sciencedaily.com/releases/2026/03/260326075552.htm

"A new study reveals that high doses of antioxidants—often seen as harmless or beneficial—may actually impact future generations. "

The dose doesn't seem that high "127 mg/kg/day N-acetylcysteine (Figures 1B,C) and 0.013 mg/kg/day selenium ", that works out to a male human equivalent dose of ~ 929 mg NAC and 0.095 mg Se. The NAC + Se was given to mice orally in their water supply, with stevia added - which also has antioxidant properties.

To calculate the equivalent dose I divided the mouse dose by 12.3 and multiplied by the average male weight in the USA, 90 kg.
https://pmc.ncbi.nlm.nih.gov/articles/PMC4804402/#T1

~
I'm wondering if the mice have pheomelanin in their testes; some animals do:
https://onlinelibrary.wiley.com/doi/abs/10.1111/pcmr.12231

Pheomelanin regulates intracellular cysteine in male finches:
https://mastodon.social/@ScienceScholar/115872514267263073

#Supplements #NAC #cysteine #selenium #stevia #anitoxidants #health

This popular supplement may increase risk of birth defects, study finds
news article, 27 March 2026
https://www.sciencedaily.com/releases/2026/03/260326075552.htm

"A new study reveals that high doses of antioxidants—often seen as harmless or beneficial—may actually impact future generations. "

The dose doesn't seem that high "127 mg/kg/day N-acetylcysteine (Figures 1B,C) and 0.013 mg/kg/day selenium ", that works out to a male human equivalent dose of ~ 929 mg NAC and 0.095 mg Se. The NAC + Se was given to mice orally in their water supply, with stevia added - which also has antioxidant properties.

To calculate the equivalent dose I divided the mouse dose by 12.3 and multiplied by the average male weight in the USA, 90 kg.
https://pmc.ncbi.nlm.nih.gov/articles/PMC4804402/#T1

~
I'm wondering if the mice have pheomelanin in their testes; some animals do:
https://onlinelibrary.wiley.com/doi/abs/10.1111/pcmr.12231

Pheomelanin regulates intracellular cysteine in male finches:
https://mastodon.social/@ScienceScholar/115872514267263073

#Supplements #NAC #cysteine #selenium #stevia #anitoxidants #health

This popular supplement may increase risk of birth defects, study finds
news article, 27 March 2026
https://www.sciencedaily.com/releases/2026/03/260326075552.htm

"A new study reveals that high doses of antioxidants—often seen as harmless or beneficial—may actually impact future generations. "

The dose doesn't seem that high "127 mg/kg/day N-acetylcysteine (Figures 1B,C) and 0.013 mg/kg/day selenium ", that works out to a male human equivalent dose of ~ 929 mg NAC and 0.095 mg Se. The NAC + Se was given to mice orally in their water supply, with stevia added - which also has antioxidant properties.

To calculate the equivalent dose I divided the mouse dose by 12.3 and multiplied by the average male weight in the USA, 90 kg.
https://pmc.ncbi.nlm.nih.gov/articles/PMC4804402/#T1

~
I'm wondering if the mice have pheomelanin in their testes; some animals do:
https://onlinelibrary.wiley.com/doi/abs/10.1111/pcmr.12231

Pheomelanin regulates intracellular cysteine in male finches:
https://mastodon.social/@ScienceScholar/115872514267263073

#Supplements #NAC #cysteine #selenium #stevia #anitoxidants #health

https://www.europesays.com/ie/413741/ How the nutrient cysteine controls cancer-fighting power of T cells #AminoAcid #cancer #CancerImmunotherapy #Cell #Cysteine #Éire #Exhaustion #Health #IE #ImmuneSystem #immunotherapy #Ireland #Laboratory #pH #Proliferation #PublicHealth #Research #Sulfur #TCell #Tumor

Too many antioxidants may negatively affect future offspring

Antioxidants have been marketed as miracle supplements, touted for preventing chronic diseases and cancers; treat…
#NewsBeep #News #Health #Aging #Alcohol #Antioxidant #AU #Australia #Brain #Cell #Children #Chronic #Craniofacial #Cysteine #Dementia #DevelopmentalBiology #dna #Exercise #Infertility #MaleInfertility #medicine #OxidativeStress #research #Selenium #sperm #stress #supplements #Veterinary
https://www.newsbeep.com/au/459335/

Flight & Brains, Feathers & Hair
June 03, 2020
Adaptation to flight has a big impact on antioxidant defenses; recently this paper came up in my feed:

Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds [2020] - https://www.nature.com/articles/s41467-020-16129-4

“Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying the constitutive activation of the NRF2 master antioxidant response in Neoaves (~95% of bird species), providing an adaptive mechanism capable of counterbalancing high ROS levels. We demonstrate that a KEAP1 mutation in the Neoavian ancestor disrupted the repression of NRF2 by KEAP1, leading to constitutive NRF2 activity and decreased oxidative stress in wild Neoaves tissues and cells. Our evidence suggests this ancient mutation induced a compensatory program in NRF2-target genes with functions beyond redox regulation—including feather development—while enabling significant metabolic rate increases that avoid trade-offs with lifespan. The strategy of NRF2 activation sought by intense clinical investigation therefore appears to have also unlocked a massively successful evolutionary trajectory.

The physiological risks of constitutive NRF2 activation due to loss of KEAP1 binding have been demonstrated in vivo through KEAP1 knockout mice, which die from starvation shortly after birth from hyperkeratosis of the gastrointestinal tract, likely through overexpression of α-keratins and loricrins in squamous cells (ref. 38; Fig. 4c). In addition to α-keratins, avian skin keratinocytes also express β-keratin genes, which combine with α-keratins to form avian skin appendages (feathers, scales, claws, beaks; ref. 3). ...

This strongly suggests that the NRF2-mediated regulation of β-keratins we detected in Chicken skin has been compensated for by the loss of AREs and downregulation of ARE binding by NRF2 at Neoaves β-keratin loci. This pattern closely mirrors the loss of NRF2-mediated ARE-regulation in Neoaves GSTA2 (Fig. 4b). Together these analyses provide in vivo evidence that the evolution of NRF2-associated feather development genes may have been shaped by the constitutive activation of NRF2 in Neoaves.”

This reminded me of some work on the evolution of large brain size in humans & loss of body hair:

Hair for brain trade-off, a metabolic bypass for encephalization [2014] - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190188/

“Hair loss in humans is perplexing and raises many hypothetical explanations. This paper suggests that hair loss in humans is metabolically related to encephalization; and that hair covered hominids would have been unable to evolve large brains because of a dietary restriction of several amino acids which are essential for hair and brain development. We use simulations to imply that hair loss must have preceded increase in brain size & volume. In this respect we see hair loss as a major force in human evolution. We assume that hair reduction required favorable climatic conditions and must have been quick. Using evolutionary and ecological time scales, we pinpoint hair loss to a period around 2.2-2.4 million years ago. The dating is further supported by a rapid selection at that time of the sialic acid deletion mutation which may have protected growing human brains against calcium ion flux. In summary we view encephalization, in part, as a metabolic trade-off between hair and brain. Other biochemical changes may have intervened in the process too; and the deletion mutation of sialic acid hydroxylation may have been involved as well.

Human hair is composed of about 17% cysteine, a sulphuric amino acid noted for its ability to add rigidity to biological tissue (Table 3).”

Cysteine is also a major component of glutathione and a rate limiter for its synthesis; glutathione production is regulated through Nrf2. The Dror & Hopp 2014 paper mentions glutathione briefly; if the theory presented is correct, the increased need for glutathione synthesis is likely the major driver. In short, humans may have lost their body hair because of the increased demand for cysteine to produce glutathione which is needed to manage oxidative stress in the brain.

Birds upregulated glutathione synthesis by constitutive upregulation of Nrf2 and also avoided the problem of hyperkeratosis through downregulation of ARE binding by NRF2 at β-keratin loci. They have more glutathione, still have all their feathers, and no hyperkeratosis.

It is possible humans lost hair first, which freed up cysteine to be used for glutathione, which then allowed for encephalization.

#Birds #cysteine #evolution #flight #HumanEvolution #OxidativeStress #KEAP1 #Nrf2

Flight & Brains, Feathers & Hair
June 03, 2020
Adaptation to flight has a big impact on antioxidant defenses; recently this paper came up in my feed:

Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds [2020] - https://www.nature.com/articles/s41467-020-16129-4

“Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying the constitutive activation of the NRF2 master antioxidant response in Neoaves (~95% of bird species), providing an adaptive mechanism capable of counterbalancing high ROS levels. We demonstrate that a KEAP1 mutation in the Neoavian ancestor disrupted the repression of NRF2 by KEAP1, leading to constitutive NRF2 activity and decreased oxidative stress in wild Neoaves tissues and cells. Our evidence suggests this ancient mutation induced a compensatory program in NRF2-target genes with functions beyond redox regulation—including feather development—while enabling significant metabolic rate increases that avoid trade-offs with lifespan. The strategy of NRF2 activation sought by intense clinical investigation therefore appears to have also unlocked a massively successful evolutionary trajectory.

The physiological risks of constitutive NRF2 activation due to loss of KEAP1 binding have been demonstrated in vivo through KEAP1 knockout mice, which die from starvation shortly after birth from hyperkeratosis of the gastrointestinal tract, likely through overexpression of α-keratins and loricrins in squamous cells (ref. 38; Fig. 4c). In addition to α-keratins, avian skin keratinocytes also express β-keratin genes, which combine with α-keratins to form avian skin appendages (feathers, scales, claws, beaks; ref. 3). ...

This strongly suggests that the NRF2-mediated regulation of β-keratins we detected in Chicken skin has been compensated for by the loss of AREs and downregulation of ARE binding by NRF2 at Neoaves β-keratin loci. This pattern closely mirrors the loss of NRF2-mediated ARE-regulation in Neoaves GSTA2 (Fig. 4b). Together these analyses provide in vivo evidence that the evolution of NRF2-associated feather development genes may have been shaped by the constitutive activation of NRF2 in Neoaves.”

This reminded me of some work on the evolution of large brain size in humans & loss of body hair:

Hair for brain trade-off, a metabolic bypass for encephalization [2014] - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190188/

“Hair loss in humans is perplexing and raises many hypothetical explanations. This paper suggests that hair loss in humans is metabolically related to encephalization; and that hair covered hominids would have been unable to evolve large brains because of a dietary restriction of several amino acids which are essential for hair and brain development. We use simulations to imply that hair loss must have preceded increase in brain size & volume. In this respect we see hair loss as a major force in human evolution. We assume that hair reduction required favorable climatic conditions and must have been quick. Using evolutionary and ecological time scales, we pinpoint hair loss to a period around 2.2-2.4 million years ago. The dating is further supported by a rapid selection at that time of the sialic acid deletion mutation which may have protected growing human brains against calcium ion flux. In summary we view encephalization, in part, as a metabolic trade-off between hair and brain. Other biochemical changes may have intervened in the process too; and the deletion mutation of sialic acid hydroxylation may have been involved as well.

Human hair is composed of about 17% cysteine, a sulphuric amino acid noted for its ability to add rigidity to biological tissue (Table 3).”

Cysteine is also a major component of glutathione and a rate limiter for its synthesis; glutathione production is regulated through Nrf2. The Dror & Hopp 2014 paper mentions glutathione briefly; if the theory presented is correct, the increased need for glutathione synthesis is likely the major driver. In short, humans may have lost their body hair because of the increased demand for cysteine to produce glutathione which is needed to manage oxidative stress in the brain.

Birds upregulated glutathione synthesis by constitutive upregulation of Nrf2 and also avoided the problem of hyperkeratosis through downregulation of ARE binding by NRF2 at β-keratin loci. They have more glutathione, still have all their feathers, and no hyperkeratosis.

It is possible humans lost hair first, which freed up cysteine to be used for glutathione, which then allowed for encephalization.

#Birds #cysteine #evolution #flight #HumanEvolution #OxidativeStress #KEAP1 #Nrf2

Flight & Brains, Feathers & Hair
June 03, 2020
Adaptation to flight has a big impact on antioxidant defenses; recently this paper came up in my feed:

Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds [2020] - https://www.nature.com/articles/s41467-020-16129-4

“Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying the constitutive activation of the NRF2 master antioxidant response in Neoaves (~95% of bird species), providing an adaptive mechanism capable of counterbalancing high ROS levels. We demonstrate that a KEAP1 mutation in the Neoavian ancestor disrupted the repression of NRF2 by KEAP1, leading to constitutive NRF2 activity and decreased oxidative stress in wild Neoaves tissues and cells. Our evidence suggests this ancient mutation induced a compensatory program in NRF2-target genes with functions beyond redox regulation—including feather development—while enabling significant metabolic rate increases that avoid trade-offs with lifespan. The strategy of NRF2 activation sought by intense clinical investigation therefore appears to have also unlocked a massively successful evolutionary trajectory.

The physiological risks of constitutive NRF2 activation due to loss of KEAP1 binding have been demonstrated in vivo through KEAP1 knockout mice, which die from starvation shortly after birth from hyperkeratosis of the gastrointestinal tract, likely through overexpression of α-keratins and loricrins in squamous cells (ref. 38; Fig. 4c). In addition to α-keratins, avian skin keratinocytes also express β-keratin genes, which combine with α-keratins to form avian skin appendages (feathers, scales, claws, beaks; ref. 3). ...

This strongly suggests that the NRF2-mediated regulation of β-keratins we detected in Chicken skin has been compensated for by the loss of AREs and downregulation of ARE binding by NRF2 at Neoaves β-keratin loci. This pattern closely mirrors the loss of NRF2-mediated ARE-regulation in Neoaves GSTA2 (Fig. 4b). Together these analyses provide in vivo evidence that the evolution of NRF2-associated feather development genes may have been shaped by the constitutive activation of NRF2 in Neoaves.”

This reminded me of some work on the evolution of large brain size in humans & loss of body hair:

Hair for brain trade-off, a metabolic bypass for encephalization [2014] - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190188/

“Hair loss in humans is perplexing and raises many hypothetical explanations. This paper suggests that hair loss in humans is metabolically related to encephalization; and that hair covered hominids would have been unable to evolve large brains because of a dietary restriction of several amino acids which are essential for hair and brain development. We use simulations to imply that hair loss must have preceded increase in brain size & volume. In this respect we see hair loss as a major force in human evolution. We assume that hair reduction required favorable climatic conditions and must have been quick. Using evolutionary and ecological time scales, we pinpoint hair loss to a period around 2.2-2.4 million years ago. The dating is further supported by a rapid selection at that time of the sialic acid deletion mutation which may have protected growing human brains against calcium ion flux. In summary we view encephalization, in part, as a metabolic trade-off between hair and brain. Other biochemical changes may have intervened in the process too; and the deletion mutation of sialic acid hydroxylation may have been involved as well.

Human hair is composed of about 17% cysteine, a sulphuric amino acid noted for its ability to add rigidity to biological tissue (Table 3).”

Cysteine is also a major component of glutathione and a rate limiter for its synthesis; glutathione production is regulated through Nrf2. The Dror & Hopp 2014 paper mentions glutathione briefly; if the theory presented is correct, the increased need for glutathione synthesis is likely the major driver. In short, humans may have lost their body hair because of the increased demand for cysteine to produce glutathione which is needed to manage oxidative stress in the brain.

Birds upregulated glutathione synthesis by constitutive upregulation of Nrf2 and also avoided the problem of hyperkeratosis through downregulation of ARE binding by NRF2 at β-keratin loci. They have more glutathione, still have all their feathers, and no hyperkeratosis.

It is possible humans lost hair first, which freed up cysteine to be used for glutathione, which then allowed for encephalization.

#Birds #cysteine #evolution #flight #HumanEvolution #OxidativeStress #KEAP1 #Nrf2

Flight & Brains, Feathers & Hair
June 03, 2020
Adaptation to flight has a big impact on antioxidant defenses; recently this paper came up in my feed:

Adaptation of the master antioxidant response connects metabolism, lifespan and feather development pathways in birds [2020] - https://www.nature.com/articles/s41467-020-16129-4

“Birds (Aves) display high metabolic rates and oxygen consumption relative to mammals, increasing reactive oxygen species (ROS) formation. Although excess ROS reduces lifespan by causing extensive cellular dysfunction and damage, birds are remarkably long-lived. We address this paradox by identifying the constitutive activation of the NRF2 master antioxidant response in Neoaves (~95% of bird species), providing an adaptive mechanism capable of counterbalancing high ROS levels. We demonstrate that a KEAP1 mutation in the Neoavian ancestor disrupted the repression of NRF2 by KEAP1, leading to constitutive NRF2 activity and decreased oxidative stress in wild Neoaves tissues and cells. Our evidence suggests this ancient mutation induced a compensatory program in NRF2-target genes with functions beyond redox regulation—including feather development—while enabling significant metabolic rate increases that avoid trade-offs with lifespan. The strategy of NRF2 activation sought by intense clinical investigation therefore appears to have also unlocked a massively successful evolutionary trajectory.

The physiological risks of constitutive NRF2 activation due to loss of KEAP1 binding have been demonstrated in vivo through KEAP1 knockout mice, which die from starvation shortly after birth from hyperkeratosis of the gastrointestinal tract, likely through overexpression of α-keratins and loricrins in squamous cells (ref. 38; Fig. 4c). In addition to α-keratins, avian skin keratinocytes also express β-keratin genes, which combine with α-keratins to form avian skin appendages (feathers, scales, claws, beaks; ref. 3). ...

This strongly suggests that the NRF2-mediated regulation of β-keratins we detected in Chicken skin has been compensated for by the loss of AREs and downregulation of ARE binding by NRF2 at Neoaves β-keratin loci. This pattern closely mirrors the loss of NRF2-mediated ARE-regulation in Neoaves GSTA2 (Fig. 4b). Together these analyses provide in vivo evidence that the evolution of NRF2-associated feather development genes may have been shaped by the constitutive activation of NRF2 in Neoaves.”

This reminded me of some work on the evolution of large brain size in humans & loss of body hair:

Hair for brain trade-off, a metabolic bypass for encephalization [2014] - https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4190188/

“Hair loss in humans is perplexing and raises many hypothetical explanations. This paper suggests that hair loss in humans is metabolically related to encephalization; and that hair covered hominids would have been unable to evolve large brains because of a dietary restriction of several amino acids which are essential for hair and brain development. We use simulations to imply that hair loss must have preceded increase in brain size & volume. In this respect we see hair loss as a major force in human evolution. We assume that hair reduction required favorable climatic conditions and must have been quick. Using evolutionary and ecological time scales, we pinpoint hair loss to a period around 2.2-2.4 million years ago. The dating is further supported by a rapid selection at that time of the sialic acid deletion mutation which may have protected growing human brains against calcium ion flux. In summary we view encephalization, in part, as a metabolic trade-off between hair and brain. Other biochemical changes may have intervened in the process too; and the deletion mutation of sialic acid hydroxylation may have been involved as well.

Human hair is composed of about 17% cysteine, a sulphuric amino acid noted for its ability to add rigidity to biological tissue (Table 3).”

Cysteine is also a major component of glutathione and a rate limiter for its synthesis; glutathione production is regulated through Nrf2. The Dror & Hopp 2014 paper mentions glutathione briefly; if the theory presented is correct, the increased need for glutathione synthesis is likely the major driver. In short, humans may have lost their body hair because of the increased demand for cysteine to produce glutathione which is needed to manage oxidative stress in the brain.

Birds upregulated glutathione synthesis by constitutive upregulation of Nrf2 and also avoided the problem of hyperkeratosis through downregulation of ARE binding by NRF2 at β-keratin loci. They have more glutathione, still have all their feathers, and no hyperkeratosis.

It is possible humans lost hair first, which freed up cysteine to be used for glutathione, which then allowed for encephalization.

#Birds #cysteine #evolution #flight #HumanEvolution #OxidativeStress #KEAP1 #Nrf2

@ScienceScholar

This is really interesting, especially that there a sex difference.

I'd like to write something about why, but am unable to do so at present.

Here's a old blog post I wrote on the topic of cysteine in birds and humans:

Flight & Brains, Feathers & Hair
June 03, 2020
https://rhyobrain.blogspot.com/2020/06/flight-brains-feathers-hair.html

#cysteine #Nrf2 #HumanEvolution #Birds #glutathione #OxidativeStress

@ScienceScholar

This is really interesting, especially that there a sex difference.

I'd like to write something about why, but am unable to do so at present.

Here's a old blog post I wrote on the topic of cysteine in birds and humans:

Flight & Brains, Feathers & Hair
June 03, 2020
https://rhyobrain.blogspot.com/2020/06/flight-brains-feathers-hair.html

#cysteine #Nrf2 #HumanEvolution #Birds #glutathione #OxidativeStress

@ScienceScholar

This is really interesting, especially that there a sex difference.

I'd like to write something about why, but am unable to do so at present.

Here's a old blog post I wrote on the topic of cysteine in birds and humans:

Flight & Brains, Feathers & Hair
June 03, 2020
https://rhyobrain.blogspot.com/2020/06/flight-brains-feathers-hair.html

#cysteine #Nrf2 #HumanEvolution #Birds #glutathione #OxidativeStress

@ScienceScholar

This is really interesting, especially that there a sex difference.

I'd like to write something about why, but am unable to do so at present.

Here's a old blog post I wrote on the topic of cysteine in birds and humans:

Flight & Brains, Feathers & Hair
June 03, 2020
https://rhyobrain.blogspot.com/2020/06/flight-brains-feathers-hair.html

#cysteine #Nrf2 #HumanEvolution #Birds #glutathione #OxidativeStress

Through a series of experiments in mice, the team discovered that changing the amount of these amino acids in the animals’ diet produced effects comparable to continuous cold exposure at five degrees Celsius.

#WeightLoss
#thermogenesis
#methionine
#cysteine

Scientists Discover a Diet That Burns Fat Like Cold Exposure, Leading to Significant Weight Loss

By tweaking just two amino acids in the diet, researchers found a way to mimic the fat-burning effects of cold exposure.

Their work centered on two amino acids, methionine and cysteine.

https://scitechdaily.com/scientists-discover-a-diet-that-burns-fat-like-cold-exposure-leading-to-significant-weight-loss/

#WeightLoss
#thermogenesis
#methionine
#cysteine

New blood test detects early-stage solid tumors with high accuracy

Current methods for cancer diagnosis are based on identifying biomarkers – molecules that reveal a particular state or…
#NewsBeep #News #Health #Artificialintelligence #AU #Australia #Blood #Cancer #CancerDiagnosis #Cysteine #Diagnostics #Hospital #ImmuneSystem #Reagents #research
https://www.newsbeep.com/au/35755/

A new study by Hacham et al. suggests a novel #regulatory feedback loop involving #glutathione, #methionine, & #cysteine, providing insight into the interrelationship between #plant growth, stress response, and #nutritional value.
https://doi.org/10.1111/jipb.13799
@wileyplantsci
#PlantSci #botany

Researchers discover how #cysteine activates a key #regulator of #cell #growth in #yeast.

#TORC1 #Pib2

https://phys.org/news/2023-12-cysteine-key-cell-growth-yeast.html

Researchers discover how #cysteine activates a key #regulator of #cell #growth in #yeast.

#TORC1 #Pib2

https://phys.org/news/2023-12-cysteine-key-cell-growth-yeast.html

My morning #supplements:
- #Organic #multivitamin
- #StJohnsWort
- #Ginseng
- #Ginko
- #PineBark
- #5HTP
- #Choline
- #Cysteine
- #Carnitine
- #Taurine
- #Tyrosine
- #Glucosamine
- #D3
- #vitaminC gummy
- #krillOil
- #probiotic

My morning #supplements:
- #Organic #multivitamin
- #StJohnsWort
- #Ginseng
- #Ginko
- #PineBark
- #5HTP
- #Choline
- #Cysteine
- #Carnitine
- #Taurine
- #Tyrosine
- #Glucosamine
- #D3
- #vitaminC gummy
- #krillOil
- #probiotic

My morning #supplements:
- #Organic #multivitamin
- #StJohnsWort
- #Ginseng
- #Ginko
- #PineBark
- #5HTP
- #Choline
- #Cysteine
- #Carnitine
- #Taurine
- #Tyrosine
- #Glucosamine
- #D3
- #vitaminC gummy
- #krillOil
- #probiotic

My morning #supplements:
- #Organic #multivitamin
- #StJohnsWort
- #Ginseng
- #Ginko
- #PineBark
- #5HTP
- #Choline
- #Cysteine
- #Carnitine
- #Taurine
- #Tyrosine
- #Glucosamine
- #D3
- #vitaminC gummy
- #krillOil
- #probiotic

My morning #supplements:
- #Organic #multivitamin
- #StJohnsWort
- #Ginseng
- #Ginko
- #PineBark
- #5HTP
- #Choline
- #Cysteine
- #Carnitine
- #Taurine
- #Tyrosine
- #Glucosamine
- #D3
- #vitaminC gummy
- #krillOil
- #probiotic

#Redox-sensitive #oligomerization of specific #cysteine residues makes #autophagy receptor #NDP52 a sensor of ROS from damaged #mitochondria, which initiates #PINK1/#Parkin-mediated #mitophagy

Victor Korolchuk and collaborators, University of Newcastle

https://www.embopress.org/doi/10.15252/embj.2022111372

#Redox-sensitive #oligomerization of specific #cysteine residues makes #autophagy receptor #NDP52 a sensor of ROS from damaged #mitochondria, which initiates #PINK1/#Parkin-mediated #mitophagy

Victor Korolchuk and collaborators, University of Newcastle

https://www.embopress.org/doi/10.15252/embj.2022111372

#Redox-sensitive #oligomerization of specific #cysteine residues makes #autophagy receptor #NDP52 a sensor of ROS from damaged #mitochondria, which initiates #PINK1/#Parkin-mediated #mitophagy

Victor Korolchuk and collaborators, University of Newcastle

https://www.embopress.org/doi/10.15252/embj.2022111372

#Redox-sensitive #oligomerization of specific #cysteine residues makes #autophagy receptor #NDP52 a sensor of ROS from damaged #mitochondria, which initiates #PINK1/#Parkin-mediated #mitophagy

Victor Korolchuk and collaborators, University of Newcastle

https://www.embopress.org/doi/10.15252/embj.2022111372