LDS Freedom Forum

nightlight wrote: ↑November 28th, 2021, 5:06 pm The last lockdown ended my job, if there's another one... I'm confident I'll be out of my current job

NeveR wrote: ↑November 27th, 2021, 6:37 am...
How much more blatant does it need to get before we all accept this has to nothing do with ANYTHING real. ALL the 'variants' are scariants, made up as needed to keep the narrative going. It's just an increasingly transparent psyop to scare and imprison us all.

Sooner or later we are going to be presented with the 'variant' caused by 'taking ivermectin while already infected'.

Cue total worldwide ban on manufacture or sale of that drug.

tribrac wrote: ↑November 28th, 2021, 8:38 pm...almost like they were reading from a script.

South African governmental adviser Professor Barry Schoub has described the Omicron symptoms as “mild” for “the great majority of the patients” infected with the new Covid-19 strain. “Their symptoms were so different and so mild from those I had treated before,” South African Medical Association chair Dr. Angelique Coetzee told The Telegraph on Saturday.

InfoWarrior82 wrote: ↑November 29th, 2021, 5:39 am Aaaaaaannnnd they've actually done it lol

Studies into heart inflammation after Covid vaccinations support that view. In two studies of more than seven million people who had received the Pfizer vaccine, it identified the risk of developing the heart condition known as myocardities is about one in 50,000.

In contrast, from the earliest days of the Covid pandemic it was clear that the coronavirus itself was a cause of an abormal number of heart issues.

Niemand wrote: ↑November 29th, 2021, 6:50 am

InfoWarrior82 wrote: ↑November 29th, 2021, 5:39 am Aaaaaaannnnd they've actually done it lol

Of course this means that people who take strokes and heart attacks - and some of them will because of neither the virus nor the injections - will be put into the victims bracket.

They are even blaming the collapsing sports players on Covid now:
viewtopic.php?f=1&t=64123

Studies into heart inflammation after Covid vaccinations support that view. In two studies of more than seven million people who had received the Pfizer vaccine, it identified the risk of developing the heart condition known as myocardities is about one in 50,000.

In contrast, from the earliest days of the Covid pandemic it was clear that the coronavirus itself was a cause of an abormal number of heart issues.

Of course, logically, if they both cause heart issues, it would suggest that something in the viral make up and the mRNA injections causes this. But they won't go there. (If you take the view that there are a lot more nasties lurking in the injections or Covid doesn't exist, that's a whole other ballgame.)

p.s. It mentions "brain fog" as a symptom. I have had several people tell me they had that after their injections.

Niemand wrote: ↑November 29th, 2021, 6:50 am

InfoWarrior82 wrote: ↑November 29th, 2021, 5:39 am Aaaaaaannnnd they've actually done it lol

Of course this means that people who take strokes and heart attacks - and some of them will because of neither the virus nor the injections - will be put into the victims bracket.

They are even blaming the collapsing sports players on Covid now:
viewtopic.php?f=1&t=64123

Studies into heart inflammation after Covid vaccinations support that view. In two studies of more than seven million people who had received the Pfizer vaccine, it identified the risk of developing the heart condition known as myocardities is about one in 50,000.

In contrast, from the earliest days of the Covid pandemic it was clear that the coronavirus itself was a cause of an abormal number of heart issues.

Of course, logically, if they both cause heart issues, it would suggest that something in the viral make up and the mRNA injections causes this. But they won't go there. (If you take the view that there are a lot more nasties lurking in the injections or Covid doesn't exist, that's a whole other ballgame.)

p.s. It mentions "brain fog" as a symptom. I have had several people tell me they had that after their injections.

Subcomandante wrote: ↑November 29th, 2021, 3:36 pm The mRNA technology is the only technology that uses the spike proteins. That in itself is concerning.

The Johnson & Johnson vaccine is slightly different. It uses double-stranded DNA inserted into a common, but inert virus called an adenovirus. This DNA also contains the instructions for building the spike protein. Once inside the cell, these instructions are read and translated into mRNA.

The mRNA chains are basically work orders that spell out the instructions for making the spike proteins that stud the outside of the coronavirus that cases COVID-19.

Messenger RNA (mRNA) is a single-stranded RNA molecule that is complementary to one of the DNA strands of a gene. The mRNA is an RNA version of the gene that leaves the cell nucleus and moves to the cytoplasm where proteins are made. During protein synthesis, an organelle called a ribosome moves along the mRNA, reads its base sequence, and uses the genetic code to translate each three-base triplet, or codon, into its corresponding amino acid.

Once the mRNA arrives, the cell can produce particular proteins from these instructions.

By injecting cells with a synthetic mRNA that encodes a viral spike protein, an mRNA vaccine can direct human cells to make a viral spike protein and evoke an immune response without a person ever having been exposed to the viral material.

This chapter describes our current understanding of the mechanisms involved in coronavirus mRNA translation and changes in host mRNA translation observed in coronavirus-infected cells.

Vaccine RQ3012-Spike encodes the full-length wild-type S, while RQ3013-VLP is formulated from a cocktail of mRNAs encoding three structural proteins: S, M (membrane), and E (envelope) to form SARS-CoV-2 virus-like particles (VLPs). To increase the expression capacity of mRNA vaccines, all mRNAs were subjected to an in-depth sequence optimization procedure of two parameters: codons in the DNA template and modified nucleotides incorporated into mRNA. We designed ten coding sequences of the S gene (3822 nucleotides in length) with varying GC-content, maintaining the maximum codon adaptation index.

CureVac AG discovered that human mRNA codons rarely have A or U at the third position and patented a strategy that replaces A or U at the third position in the open reading frame with G or C21.

The two most frequently used SARS-CoV-2 vaccines, from Pfizer/BioNTech [1] and Moderna [2], respectively, are both mRNA vaccines. The sequence of Pfizer/BioNTech’s BNT-162b2 is publicly available [3], and the sequence of Moderna’s mRNA-1273 has recently been sequenced [4]. Both mRNA encodes the same S-2P protein [5,6] which differ from the spike protein in the reference SARS-CoV-2 genome (NC_045512) by two amino acids, i.e., amino acids KV at sites 986 and 987 were replaced by PP to stabilize the resulting spike protein in the prefusion state to train the host immune system to recognize the virus before its entry into the host cell [7,8].

While the Pfizer/BioNTech’s BNT162b2 mRNA and Moderna’s mRNA-1273 share the same amino acid sequence, they differ in many other ways, such as the design of 5′-UTR, codon optimization and 3′-UTR. Translation initiation is typically the limiting step in translation, and its efficiency depends heavily on how rapidly the 5′-UTR can load ribosome onto the mRNA [9]. Translation elongation becomes rate-limiting when translation initiation is highly efficient [10,11]. Optimization of vaccine mRNA for efficient translation can decrease the copies of vaccine mRNA needed to be carried into host cells.

other papers showed that the spike protein by itself (without being part of the corona virus) can damage endothelial cells and disrupt the blood-brain barrier.

Even if it could get into the nucleus, the single strand of mRNA would have to be translated back into a double stranded DNA.

HIV, the virus that causes AIDS, can do this. It uses an enzyme like reverse transcriptase to insert itself into our chromosomes. The mRNA in the vaccines lacks this enzyme, so it can't turn back into DNA.

The DNA adenovirus used in the Johnson & Johnson vaccine does enter the nucleus of our cells, but it never integrates into our chromosomes.

The first U in the stop codon in translating AZ1 mRNA is often skipped when the concentration of polyamines is high, resulting in the ribosome reading GAU as the next codon [85]. With such a +1 frameshifting, a downstream in-frame stop codon cannot serve as a fail-safe mechanism. UGA is a poor choice of a stop codon, and UGAU in Pfizer/BioNTech and Moderna mRNA vaccines could be even worse.

As Ψ is more promiscuous in base-pairing than U and can pair with both A and G and, to a less extent, with C and U [16], stop codons become more prone to misreading by tRNAs [17]. It is for this reason that both mRNA vaccines use consecutive stop codons as a fail-safe mechanism, with the hope that no frameshifting occurs when the first stop codon fails. However, UGAU is known to cause a +1 frameshifting. It is reasonable to infer that ΨGAΨ may be the same.

Codon bias has been implicated as one of the major factors contributing to mRNA stability in several model organisms. However, the molecular mechanisms of codon bias on mRNA stability remain unclear in humans.

The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences
that may induce TDP-43 and FUS to fold into their pathologic prion confirmations

Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.

mRNA-based COVID shots have used codon optimization to improve protein production. A codon consists of three nucleotides, and nucleotides are the building blocks of DNA. Use of codon optimization virtually guarantees unexpected results

Replacing rare codons must be done judiciously, as rarer codons can have slower translation rates and a slowed-down rate is actually necessary to prevent protein misfolding

Stop codons, when present at the end of an mRNA coding sequence, signals the termination of protein synthesis. According to a recent paper, both Pfizer and Moderna selected suboptimal stop codons

The COVID shots induce spike protein at levels unheard of in nature, and the spike protein is the toxic part of the virus responsible for the most unique effects of the virus, such as the blood clotting disorders, neurological problems and heart damage. To expect the COVID shot to not produce these kinds of effects would be rather naïve

Other significant threats include immune dysfunction and the flare-up of latent viral infections such as herpes and shingles. Coinfections, in turn, could accelerate other diseases. Herpes viruses, for example, have been implicated as a cause of both AIDS and chronic fatigue syndrome

Jason wrote: ↑November 29th, 2021, 4:14 pm

Subcomandante wrote: ↑November 29th, 2021, 3:36 pm The mRNA technology is the only technology that uses the spike proteins. That in itself is concerning.

...mRNA is just the type of genetic programming for the body to create spike proteins...the genetic therapy to make the human body a spike protein factory is not limited to mRNA "vaccines"...the "mRNA technology doesn't USE the spike proteins"...it is instructions for the body to manufacture them...

The Johnson & Johnson vaccine is slightly different. It uses double-stranded DNA inserted into a common, but inert virus called an adenovirus. This DNA also contains the instructions for building the spike protein. Once inside the cell, these instructions are read and translated into mRNA.

The mRNA chains are basically work orders that spell out the instructions for making the spike proteins that stud the outside of the coronavirus that cases COVID-19.

https://www.webmd.com/lung/news/2021071 ... ne-therapy

...that's from mainstream....

Messenger RNA (mRNA) is a single-stranded RNA molecule that is complementary to one of the DNA strands of a gene. The mRNA is an RNA version of the gene that leaves the cell nucleus and moves to the cytoplasm where proteins are made. During protein synthesis, an organelle called a ribosome moves along the mRNA, reads its base sequence, and uses the genetic code to translate each three-base triplet, or codon, into its corresponding amino acid.

https://www.genome.gov/genetics-glossary/messenger-rna

Once the mRNA arrives, the cell can produce particular proteins from these instructions.

https://www.civilbeat.org/2021/04/what- ... t-it-does/

By injecting cells with a synthetic mRNA that encodes a viral spike protein, an mRNA vaccine can direct human cells to make a viral spike protein and evoke an immune response without a person ever having been exposed to the viral material.

https://www.genome.gov/about-genomics/f ... A-Vaccines

This chapter describes our current understanding of the mechanisms involved in coronavirus mRNA translation and changes in host mRNA translation observed in coronavirus-infected cells.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388242/

...the technology encodes the same full sequence spike protein that the wild caught virus utilizes...but they took some shortcuts...

Vaccine RQ3012-Spike encodes the full-length wild-type S, while RQ3013-VLP is formulated from a cocktail of mRNAs encoding three structural proteins: S, M (membrane), and E (envelope) to form SARS-CoV-2 virus-like particles (VLPs). To increase the expression capacity of mRNA vaccines, all mRNAs were subjected to an in-depth sequence optimization procedure of two parameters: codons in the DNA template and modified nucleotides incorporated into mRNA. We designed ten coding sequences of the S gene (3822 nucleotides in length) with varying GC-content, maintaining the maximum codon adaptation index.

https://www.nature.com/articles/s41422-020-00392-7

CureVac AG discovered that human mRNA codons rarely have A or U at the third position and patented a strategy that replaces A or U at the third position in the open reading frame with G or C21.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386155/

The two most frequently used SARS-CoV-2 vaccines, from Pfizer/BioNTech [1] and Moderna [2], respectively, are both mRNA vaccines. The sequence of Pfizer/BioNTech’s BNT-162b2 is publicly available [3], and the sequence of Moderna’s mRNA-1273 has recently been sequenced [4]. Both mRNA encodes the same S-2P protein [5,6] which differ from the spike protein in the reference SARS-CoV-2 genome (NC_045512) by two amino acids, i.e., amino acids KV at sites 986 and 987 were replaced by PP to stabilize the resulting spike protein in the prefusion state to train the host immune system to recognize the virus before its entry into the host cell [7,8].

While the Pfizer/BioNTech’s BNT162b2 mRNA and Moderna’s mRNA-1273 share the same amino acid sequence, they differ in many other ways, such as the design of 5′-UTR, codon optimization and 3′-UTR. Translation initiation is typically the limiting step in translation, and its efficiency depends heavily on how rapidly the 5′-UTR can load ribosome onto the mRNA [9]. Translation elongation becomes rate-limiting when translation initiation is highly efficient [10,11]. Optimization of vaccine mRNA for efficient translation can decrease the copies of vaccine mRNA needed to be carried into host cells.

...and the spike protein is toxic all by itself...so getting vaccinated is getting genetic programming for the body to manufacture a toxin (spike protein)...

other papers showed that the spike protein by itself (without being part of the corona virus) can damage endothelial cells and disrupt the blood-brain barrier.

https://pubmed.ncbi.nlm.nih.gov/34100279/

...and they make claims about what can and can't happen...but they don't know for sure...

Even if it could get into the nucleus, the single strand of mRNA would have to be translated back into a double stranded DNA.

HIV, the virus that causes AIDS, can do this. It uses an enzyme like reverse transcriptase to insert itself into our chromosomes. The mRNA in the vaccines lacks this enzyme, so it can't turn back into DNA.

The DNA adenovirus used in the Johnson & Johnson vaccine does enter the nucleus of our cells, but it never integrates into our chromosomes.

https://www.webmd.com/lung/news/2021071 ... ne-therapy

The first U in the stop codon in translating AZ1 mRNA is often skipped when the concentration of polyamines is high, resulting in the ribosome reading GAU as the next codon [85]. With such a +1 frameshifting, a downstream in-frame stop codon cannot serve as a fail-safe mechanism. UGA is a poor choice of a stop codon, and UGAU in Pfizer/BioNTech and Moderna mRNA vaccines could be even worse.

As Ψ is more promiscuous in base-pairing than U and can pair with both A and G and, to a less extent, with C and U [16], stop codons become more prone to misreading by tRNAs [17]. It is for this reason that both mRNA vaccines use consecutive stop codons as a fail-safe mechanism, with the hope that no frameshifting occurs when the first stop codon fails. However, UGAU is known to cause a +1 frameshifting. It is reasonable to infer that ΨGAΨ may be the same.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310186/

Codon usage is an important determinant of gene expression levels largely through its effects on transcription
https://www.pnas.org/content/113/41/E6117

...more of a currently held belief....that we'll be able in a decade or so to address more fully...

Codon bias has been implicated as one of the major factors contributing to mRNA stability in several model organisms. However, the molecular mechanisms of codon bias on mRNA stability remain unclear in humans.

https://www.embopress.org/doi/full/10.1 ... .201948220

The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences
that may induce TDP-43 and FUS to fold into their pathologic prion confirmations

Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.

https://dundasvalley.files.wordpress.co ... e-1503.pdf

Reverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient-derived tissues
https://www.pnas.org/content/118/21/e2105968118

....so to summarize...courtesy of Dr. Mercola...

mRNA-based COVID shots have used codon optimization to improve protein production. A codon consists of three nucleotides, and nucleotides are the building blocks of DNA. Use of codon optimization virtually guarantees unexpected results

Replacing rare codons must be done judiciously, as rarer codons can have slower translation rates and a slowed-down rate is actually necessary to prevent protein misfolding

Stop codons, when present at the end of an mRNA coding sequence, signals the termination of protein synthesis. According to a recent paper, both Pfizer and Moderna selected suboptimal stop codons

The COVID shots induce spike protein at levels unheard of in nature, and the spike protein is the toxic part of the virus responsible for the most unique effects of the virus, such as the blood clotting disorders, neurological problems and heart damage. To expect the COVID shot to not produce these kinds of effects would be rather naïve

Other significant threats include immune dysfunction and the flare-up of latent viral infections such as herpes and shingles. Coinfections, in turn, could accelerate other diseases. Herpes viruses, for example, have been implicated as a cause of both AIDS and chronic fatigue syndrome

https://www.nutritruth.org/single-post/ ... king-about

TrueFaith wrote: ↑November 29th, 2021, 3:26 pm "Put on the whole armour of God, that ye may be able to stand against the wiles of the devil. For we wrestle not against flesh and blood, but against principalities, against powers, against the rulers of the darkness of this world, against spiritual wickedness in high places."
Ephesians 6:11-12

Keep reminding yourself that this is a spiritual war. Literally. Those of us who are not submitting to this evil are going to be a target for the evil spirits around us who are angry that we will not submit.

I was sitting out in my shed today (I use it as an office) and was listening to the video below. At the mention of Christ, objects began falling and moving from their place around me in the room. I knelt and blessed the building a few minutes ago by the power of the Priesthood and in the name of Jesus Christ.

Things have been and are ramping up. I keep reminding everyone that Angels and Demons are real, cast out the demons, and pray for the help of the angels.

Niemand wrote: ↑November 29th, 2021, 7:47 pm

TrueFaith wrote: ↑November 29th, 2021, 3:26 pm "Put on the whole armour of God, that ye may be able to stand against the wiles of the devil. For we wrestle not against flesh and blood, but against principalities, against powers, against the rulers of the darkness of this world, against spiritual wickedness in high places."
Ephesians 6:11-12

Keep reminding yourself that this is a spiritual war. Literally. Those of us who are not submitting to this evil are going to be a target for the evil spirits around us who are angry that we will not submit.

I was sitting out in my shed today (I use it as an office) and was listening to the video below. At the mention of Christ, objects began falling and moving from their place around me in the room. I knelt and blessed the building a few minutes ago by the power of the Priesthood and in the name of Jesus Christ.

Things have been and are ramping up. I keep reminding everyone that Angels and Demons are real, cast out the demons, and pray for the help of the angels.

We've discussed this elsewhere, but it sounds as if you have some nasties attached either to yourself, for whatever reason, or to your home. You have obviously made an effort to expel them from some places. You either need to do something to exorcise the entire place you live in, or to pray to be released from whatever is linking them to you and your family. From what you tell me there is evidence that they were there before you moved in.

Personally I would order them out in the name of Jesus Christ making sure to add "and not return".

TrueFaith wrote: ↑November 29th, 2021, 7:50 pm This is brand new. Started a couple weeks ago. My guess is whatever I cast out of my home found its way into my office shed.

I've been having spirit and angelic encounters for the past year and half now exactly since Covid started in Mar 2020. I'm so used to it now it's barely shocking to me anymore.

Believe me, I've changed nothing in my personal life since before then. I'm convinced the common thread is not me, it's the rollout of the Beast system. The beings beyond the veil are on hyperdrive.

Niemand wrote: ↑November 30th, 2021, 4:09 am

TrueFaith wrote: ↑November 29th, 2021, 7:50 pm This is brand new. Started a couple weeks ago. My guess is whatever I cast out of my home found its way into my office shed.

Expel these things off your property, all of it, and pray a hedge of protection around it and your loved ones. They also don't like crosses, although I know that isn't LDS teaching.

I've been having spirit and angelic encounters for the past year and half now exactly since Covid started in Mar 2020. I'm so used to it now it's barely shocking to me anymore.

Be careful some of these are not one posing as the other.

Believe me, I've changed nothing in my personal life since before then. I'm convinced the common thread is not me, it's the rollout of the Beast system. The beings beyond the veil are on hyperdrive.

I haven't had such experiences at home in the last eighteen months. I keep thinking it's because they're busy elsewhere. Had a book fall off a shelf recently, but that was more to do with how I'd crammed it on there with anything else. (It is possible that your sound system, or even vibrations from wind etc knocked things over) If I do feel a bad atmosphere at home, I often play some hymns and it seems to get rid of it.

Think of it another way. This will be a very busy period for them. It is their job to get things done elsewhere and they are also fighting their spiritual opposition at an increased level just now. You're actually low down the food chain, but you have the authority to send them packing, and can do so. You may, ironically, have encountered some of their more reluctant warriors. Their main job is to influence leaders, increase crime and hatred, drive people to despair etc just now.

NB - you may have done nothing recently to draw them in, but there may be something in your history that draws them in, but from what you tell me they were there before Covid, and you even moved in.

InfoWarrior82 wrote: ↑November 29th, 2021, 5:57 pm

Jason wrote: ↑November 29th, 2021, 4:14 pm

Subcomandante wrote: ↑November 29th, 2021, 3:36 pm The mRNA technology is the only technology that uses the spike proteins. That in itself is concerning.

...mRNA is just the type of genetic programming for the body to create spike proteins...the genetic therapy to make the human body a spike protein factory is not limited to mRNA "vaccines"...the "mRNA technology doesn't USE the spike proteins"...it is instructions for the body to manufacture them...

The Johnson & Johnson vaccine is slightly different. It uses double-stranded DNA inserted into a common, but inert virus called an adenovirus. This DNA also contains the instructions for building the spike protein. Once inside the cell, these instructions are read and translated into mRNA.

The mRNA chains are basically work orders that spell out the instructions for making the spike proteins that stud the outside of the coronavirus that cases COVID-19.

https://www.webmd.com/lung/news/2021071 ... ne-therapy

...that's from mainstream....

Messenger RNA (mRNA) is a single-stranded RNA molecule that is complementary to one of the DNA strands of a gene. The mRNA is an RNA version of the gene that leaves the cell nucleus and moves to the cytoplasm where proteins are made. During protein synthesis, an organelle called a ribosome moves along the mRNA, reads its base sequence, and uses the genetic code to translate each three-base triplet, or codon, into its corresponding amino acid.

https://www.genome.gov/genetics-glossary/messenger-rna

Once the mRNA arrives, the cell can produce particular proteins from these instructions.

https://www.civilbeat.org/2021/04/what- ... t-it-does/

By injecting cells with a synthetic mRNA that encodes a viral spike protein, an mRNA vaccine can direct human cells to make a viral spike protein and evoke an immune response without a person ever having been exposed to the viral material.

https://www.genome.gov/about-genomics/f ... A-Vaccines

This chapter describes our current understanding of the mechanisms involved in coronavirus mRNA translation and changes in host mRNA translation observed in coronavirus-infected cells.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388242/

...the technology encodes the same full sequence spike protein that the wild caught virus utilizes...but they took some shortcuts...

Vaccine RQ3012-Spike encodes the full-length wild-type S, while RQ3013-VLP is formulated from a cocktail of mRNAs encoding three structural proteins: S, M (membrane), and E (envelope) to form SARS-CoV-2 virus-like particles (VLPs). To increase the expression capacity of mRNA vaccines, all mRNAs were subjected to an in-depth sequence optimization procedure of two parameters: codons in the DNA template and modified nucleotides incorporated into mRNA. We designed ten coding sequences of the S gene (3822 nucleotides in length) with varying GC-content, maintaining the maximum codon adaptation index.

https://www.nature.com/articles/s41422-020-00392-7

CureVac AG discovered that human mRNA codons rarely have A or U at the third position and patented a strategy that replaces A or U at the third position in the open reading frame with G or C21.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8386155/

The two most frequently used SARS-CoV-2 vaccines, from Pfizer/BioNTech [1] and Moderna [2], respectively, are both mRNA vaccines. The sequence of Pfizer/BioNTech’s BNT-162b2 is publicly available [3], and the sequence of Moderna’s mRNA-1273 has recently been sequenced [4]. Both mRNA encodes the same S-2P protein [5,6] which differ from the spike protein in the reference SARS-CoV-2 genome (NC_045512) by two amino acids, i.e., amino acids KV at sites 986 and 987 were replaced by PP to stabilize the resulting spike protein in the prefusion state to train the host immune system to recognize the virus before its entry into the host cell [7,8].

While the Pfizer/BioNTech’s BNT162b2 mRNA and Moderna’s mRNA-1273 share the same amino acid sequence, they differ in many other ways, such as the design of 5′-UTR, codon optimization and 3′-UTR. Translation initiation is typically the limiting step in translation, and its efficiency depends heavily on how rapidly the 5′-UTR can load ribosome onto the mRNA [9]. Translation elongation becomes rate-limiting when translation initiation is highly efficient [10,11]. Optimization of vaccine mRNA for efficient translation can decrease the copies of vaccine mRNA needed to be carried into host cells.

...and the spike protein is toxic all by itself...so getting vaccinated is getting genetic programming for the body to manufacture a toxin (spike protein)...

other papers showed that the spike protein by itself (without being part of the corona virus) can damage endothelial cells and disrupt the blood-brain barrier.

https://pubmed.ncbi.nlm.nih.gov/34100279/

...and they make claims about what can and can't happen...but they don't know for sure...

Even if it could get into the nucleus, the single strand of mRNA would have to be translated back into a double stranded DNA.

HIV, the virus that causes AIDS, can do this. It uses an enzyme like reverse transcriptase to insert itself into our chromosomes. The mRNA in the vaccines lacks this enzyme, so it can't turn back into DNA.

The DNA adenovirus used in the Johnson & Johnson vaccine does enter the nucleus of our cells, but it never integrates into our chromosomes.

https://www.webmd.com/lung/news/2021071 ... ne-therapy

The first U in the stop codon in translating AZ1 mRNA is often skipped when the concentration of polyamines is high, resulting in the ribosome reading GAU as the next codon [85]. With such a +1 frameshifting, a downstream in-frame stop codon cannot serve as a fail-safe mechanism. UGA is a poor choice of a stop codon, and UGAU in Pfizer/BioNTech and Moderna mRNA vaccines could be even worse.

As Ψ is more promiscuous in base-pairing than U and can pair with both A and G and, to a less extent, with C and U [16], stop codons become more prone to misreading by tRNAs [17]. It is for this reason that both mRNA vaccines use consecutive stop codons as a fail-safe mechanism, with the hope that no frameshifting occurs when the first stop codon fails. However, UGAU is known to cause a +1 frameshifting. It is reasonable to infer that ΨGAΨ may be the same.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8310186/

Codon usage is an important determinant of gene expression levels largely through its effects on transcription
https://www.pnas.org/content/113/41/E6117

...more of a currently held belief....that we'll be able in a decade or so to address more fully...

Codon bias has been implicated as one of the major factors contributing to mRNA stability in several model organisms. However, the molecular mechanisms of codon bias on mRNA stability remain unclear in humans.

https://www.embopress.org/doi/full/10.1 ... .201948220

The RNA sequence of the vaccine as well as the spike protein target interaction were analyzed for the potential to convert intracellular RNA binding proteins TAR DNA binding protein (TDP-43) and Fused in Sarcoma (FUS) into their pathologic prion conformations. The results indicate that the vaccine RNA has specific sequences
that may induce TDP-43 and FUS to fold into their pathologic prion confirmations

Furthermore, the spike protein, created by the translation of the vaccine RNA, binds angiotensin converting enzyme 2 (ACE2), a zinc containing enzyme. This interaction has the potential to increase intracellular zinc. Zinc ions have been shown to cause the transformation of TDP-43 to its pathologic prion configuration. The folding of TDP-43 and FUS into their pathologic prion confirmations is known to cause ALS, front temporal lobar degeneration, Alzheimer’s disease and other neurological degenerative diseases.

https://dundasvalley.files.wordpress.co ... e-1503.pdf

Reverse-transcribed SARS-CoV-2 RNA can integrate into the genome of cultured human cells and can be expressed in patient-derived tissues
https://www.pnas.org/content/118/21/e2105968118

....so to summarize...courtesy of Dr. Mercola...

mRNA-based COVID shots have used codon optimization to improve protein production. A codon consists of three nucleotides, and nucleotides are the building blocks of DNA. Use of codon optimization virtually guarantees unexpected results

Replacing rare codons must be done judiciously, as rarer codons can have slower translation rates and a slowed-down rate is actually necessary to prevent protein misfolding

Stop codons, when present at the end of an mRNA coding sequence, signals the termination of protein synthesis. According to a recent paper, both Pfizer and Moderna selected suboptimal stop codons

The COVID shots induce spike protein at levels unheard of in nature, and the spike protein is the toxic part of the virus responsible for the most unique effects of the virus, such as the blood clotting disorders, neurological problems and heart damage. To expect the COVID shot to not produce these kinds of effects would be rather naïve

Other significant threats include immune dysfunction and the flare-up of latent viral infections such as herpes and shingles. Coinfections, in turn, could accelerate other diseases. Herpes viruses, for example, have been implicated as a cause of both AIDS and chronic fatigue syndrome

https://www.nutritruth.org/single-post/ ... king-about

Bah! What could go wrong?!

With the mRNA corona "vaccination", body cells are for the first time in history deliberately and genetically programmed by means of the mRNA to produce the spike protein as a (foreign) antigen on the cell surface, although they are completely healthy and not infected with the virus.

The mechanism of action of the corona "vaccination" is to falsely mark healthy cells as foreign.

As a consequence, the immune system reacts immediately; it recognizes the antigen as foreign, forms antibodies against it and destroys the spike protein by destroying the cell that carries this spike protein. [1,2]

This means that the corona "vaccination" fools our immune system and tricks it into attacking and destroying our own healthy cells. In the military it is this is called 'friendly fire' when soldiers attack their own troops. This represents a fundamental danger not only for our health but also to our survival. We know this situation with the rarely occurring autoimmune diseases. These are usually severe and can even be fatal.

Our immune system is capable of learning. When a pathogen enters the body for the first time, it is recognized as foreign, but it takes a few days for the immune system to kick in. During this time, the pathogen has the upper hand for a short time. Only after a few days is the immune system strong enough to destroy the pathogen and we become healthy.

Fortunately, the second time, the immune system remembers the "appearance" of the pathogen and it is activated much faster and much more powerfully. This strong defense protects us and we do not fall ill again; we are immune.

This vital mechanism also takes place with every further corona "vaccination", but the massive reaction of the immune system with each further injection is not directed against a pathogen but against our own healthy body cells that have once again been marked with the spike protein. Viewed as a pathogen, this otherwise healthy cell is targeted to be destroyed. The effectiveness and ferocity of this destruction of healthy cells is increased with each injection. This means that the healthy "spiked cells" in the body are destroyed even more efficiently than in the first injection.

Thus, this memory capacity of the immune system becomes a dangerous weapon against ourselves.

Instead of making foreign pathogens harmless, the immune system now destroys the body's own cells which were instructed to produce the spike protein. Every further injection of a Corona "vaccine" consequently poses a great risk. This corresponds to the observation that more and stronger vaccination complications occur with the second vaccination.

The same applies to people who have had a Corona infection in the past, have recovered and still get a Corona "vaccination". [14,15,16,17]