Diabolical Molecule inside mRNA Vaccines generates Harmful Proteins as Killer Prions, “Brain-Eating Amoeba”. Explosive Study by prof. Perez (Montagnier Foundation)
by Fabio Giuseppe Carlo Carisio
In our complex investigation into the diabolical molecule N1-methylpseudouridine initialed “m1Ψ”, created with a double laboratory manipulation of human uridine and used in the new mRNA biotechnology of Covid vaccines, the Canadian biochemist Jessica Rose has been shocked in the analysis on the results of an investigation from the University of Cambridge (Mulroney et al.) who confirmed the alarm which she raised together with other researchers about the very dangerous DNA fragments detected in the vials of the Comirnaty (Pfizer-Biontech) and Spikevax (Moderna) genetic sera.
These fragments have been found to be extremely dangerous because they can cause cancer, as even supported by the guidelines of the Food and Drug Administration (American drug regulator) and as reported to the FDA itself by the Surgeon General of Florida who requested the immediate and complete interruption of each administration of the Covid mRNA vaccine.
In reference to the Cambridge study, Dr. Rose explained that «the paper provides evidence for the formation “off-target” or unintended proteins following vaccination with BNT162b2 due to frameshifting. Given the proposed mechanism, a similar problem is likely to exist for the Moderna product».
The Sensational Discovery of the Biomathematician Perez
Well in recent days the biomathematician Jean-Claude Perez, continuing a study started with the late biologist Luc Montagnier, managed to identify that some of those anomalous proteins can be produced in the prion regions causing new fulminant neurocerebral pathologies such as human Mad Cow Disease.
But there are traces of protein production similar to those of the brain-eating amoeba…
This was highlighted in a study published on 19 January 2024 in Zenodo (an authoritative scientific journal managed by the European Organization for Nuclear Research, commonly known by the acronym CERN). The research (link in the sources below) is still pre-print (awaiting peer review) but deals with a topic on which the author has already written other reviewed research.
Today we will limit ourselves to publishing the essential conclusions of Professor Perez, bioengineering expert and scientist of the Montagnier Foundation, referring for the more technical parts to our previous articles on the killer prions which we published in preview.
Last May, in fact, I interviewed the scientist above all about his previous and explosive research signed with Montagnier, already winner of the Nobel Prize for Medicine, with which they demonstrated, in March 2020, the artificial origin of SARS-Cov-2.
At the time they were also the subject of multiple censorship by the world scientific community but today even the Health Commission of the American Senate has reached the same conclusions in a dossier published in recent months.
The Role and Danger of Prions
Let’s first make a brief scientific introduction to biochemistry. Prions are proteins that exist naturally in the brain. They perform crucial tasks and are necessary for human health.
However, on rare occasions, a healthy prion can transform into a pathogenic prion. This misfold (i.e. this incorrect folding of the protein, ed.) is irreversible and from that moment the pathogenic prion converts all the healthy prions it encounters into pathogenic prions.
When pathogenic prions accumulate, people can begin to develop prion pathologies such as CJD, or Creutzfeldt-Jakob disease which has similar characteristics to veterinary Mad Cow syndrome in humans.
Perez and Montagnier (with the help of neurologist Claire Moret Chalmin) highlighted that 26 vaccinated people had died from this neurocerebral pathology. Affected people have reported that the first symptoms appeared one to 31 days after the last COVID-19 vaccination. All patients experienced rapid deterioration.
Other researchers have proposed that Parkinson’s disease and Alzheimer’s disease, both characterized by a buildup of misfolded proteins, may also be prion pathologies.
New Research on Harmful Proteins in mRNA Vaccines
Let’s now see what the French biomathematician concluded in the study prudently titled with a question to which he obviously gave a positive answer: “Do Covid19 modified mRNA jabs Pose a Risk of Creating Harmful Proteins or Prions?”.
«In COVID-19 mRNA vaccines, natural uracil bases are replaced with modified pseudouracil. This study investigates the potential consequences of this modification on protein synthesis. Occasionally, ribosomes may overlook these modified bases, leading to a shift in the reading frame of the genetic code. We examine the spike protein in the context of these shifted reading frames and identify the resulting proteins. Our analysis focuses on the potential formation of prion-like or amyloidogenic proteins due to this frame-shifting process» Perez wrote.
Frame-shifting consists of a “slipping” of the ribosomal structure which can have tragic consequences as the biochemist Rose warned in relation to “modified pseudouracil” or the diabolical molecule N1-methylpseudouridine:
«The modified mRNAs for use in the COVID-19 products were codon-optimized for maximal protein expression in humans. Codon optimization, or synonymous codon replacement, rests on the idea that one can induce mutations throughout a gene of interest (like spike) based on an organism’s (like humans) codon usage bias, to increase translational efficiency and protein expression without altering the sequence of the protein. But, it is well-known that codon-optimization can lead to protein conformation, folding and stability problems».
Frameshift errors occur when the cell’s protein production machinery accidentally misses one or two bases in the mRNA sequence. Since mRNA bases are read in groups of threes, a frameshift breaks up the original sets of the sequence, affecting all sequences downstream of the error.
The amyloidogenic proteins mentioned in the study can cause rare amyloidogenic vascular cerebropathies.
They, as the Telethon website focused on this pathology explains, are a group of diseases of the blood vessels of the brain characterized by the deposition of a protein called beta-amyloid. This accumulation leads to a gradual destruction of the blood vessels and consequently to the appearance of hemorrhages, which can vary in extent.
Typical symptoms may be: headache, weakness, transient loss of speech and sudden weakening of vision, nausea, vomiting. Often, hemorrhages interfere with the cognitive abilities of the affected person, who undergoes dementia and motor deficits. In the most serious forms, which arise already around 30-40 years of age, mortality is very high: 50% of patients die following the first episode of hemorrhage.
The Discovery of Parasitic Proteins
In his research, prof. Perez found a frameshift by one base retains the prion-like sequences, while a frameshift by two bases eliminates them. He also found that the frameshift sequences share similarities to bacterial proteins on the brain-eating amoeba and human nuclease proteins, proteins capable of breaking apart DNA bonds.
«Our findings also uncovered a striking homology with Naegleria fowleri, commonly known as the “brain-eating amoeba”; This discovery raises several concerns:
- The presence of Naegleria fowleri traces could be linked to the uninterpreted pseudo-uridine bases in the ribosome, a scenario increasingly probable considering the widespread use of mRNA protein injections since 2021.
- The resurgence of this disease has been noted concurrently with COVID-19 vaccine rollouts, particularly highlighted in regions like Texas and Pakistan».
His words become increasingly chilling because they confirm the fears expressed by other researchers.
«Our investigation, while focusing on a limited subset of possible unintended proteins resulting from mRNA COVID-19 vaccinations, has revealed noteworthy findings that merit serious consideration. The scope of potential off-target proteins is vast, yet even within our constrained analysis, significant observations have been made».
Observations of Parasitic Proteins
«A notable aspect of our study is the identification of parasitic proteins, many of which were discovered post-2020. This timeline coincides with the widespread administration of COVID-19 vaccines. The emergence of these proteins during the same period suggests a possible link to the vaccine’s mRNA technology and its unintended consequences».
The Implications of a Potential Prion Region
«Our analysis identified not only unknown proteins but also the presence of a potential prion region. This finding is particularly concerning due to the inherent risks associated with prion diseases and their impact on neurological health. The discovery of a prion-like sequence within the altered spike protein emphasizes the need for rigorous examination of mRNA vaccine components and their long-term effects».
The Pervasive Use of Pseudo-Uridine Technology
«The use of pseudo-uridine technology in mRNA vaccines has been universal, affecting billions of inoculations and encompassing various iterations of the vaccine, including those targeting both the original Wuhan strain and the subsequent Omicron variant. This widespread application raises concerns about the broad impact of any unintended protein creation across different vaccine batches and formulations».
Omicron Laboratory Nightmare and Vaccine Safety Appeal
The most attentive readers of Gospa News know well that some Japanese researchers highlighted the presumed laboratory origin of the Omicron variant (now dominant with the derivative genotypes of Kraken, on which the new monovalent mRNA vaccines from Pfizer and Moderna have been updated, and the new one still little known and therefore feared JN.1) as Perez himself had hypothesized precisely due to the disappearance of the prion region in this variant.
The new research by the French biomathematician from the Montagnier Foundation concludes with a heartfelt appeal to the health authorities who continue to recommend mRNA vaccines especially to fragile patients even though there are no studies on the effectiveness and safety for this category of people.
Indeed Perez concluded his study thus:
«The findings of our study, while preliminary, highlight the critical need for comprehensive research into the full spectrum of potential off-target effects of mRNA COVID-19 vaccines. The detection of unknown proteins and prion-like regions, particularly in the context of a technology as widespread as pseudo-uridine modification, calls for a cautious approach. It underscores the importance of ongoing monitoring and evaluation of vaccine safety, especially as new formulations are developed and deployed globally.The potential implications for public health are significant, warranting continued vigilance and investigation into the molecular intricacies and long- term effects of these novel medical interventions».
Big Pharma business despite the Turbo-Cancer Alarm
But the Big Pharma business cannot wait and continues even though genotoxicity and carcinogenicity have not been thoroughly studied.
In addition to neurocerebral pathologies such as the CJD disease reported by Perez, today biochemists and immunologists are worried about both the very serious muscular inflammatory implications (especially in the cardiac system) caused by the dangerous lipid nanoparticles, and the turbo-cancers that can derive precisely from the diabolical molecule N1 -methylpseudouridine…
Because as wrote the American biophysics Stephanie Seneff (researcher at the prestigious MIT – Massachusetts Institute of Technology) and then the Italian bio-immunologist Mauro Mantovani confirmed, «The many alterations in the vaccine mRNA hide the mRNA from cellular defenses and promote a longer biological half-life and high production of spike protein».
But most importantly Seneff added:
«Immune cells that have taken up the vaccine nanoparticles release into circulation large numbers of exosomes containing spike protein along with critical microRNAs that induce a signaling response in recipient cells at distant sites. We also identify potential profound disturbances in regulatory control of protein synthesis and cancer surveillance».
The Surgeon General of Florida has reported to the FDA precisely the danger that the DNA fragments produce an oncogenic reaction resulting from the new mRNA biotechnologies of which, moreover, Moderna has been aware since 2019.
Fabio Giuseppe Carlo Carisio
© COPYRIGHT GOSPA NEWS
prohibition of reproduction without authorization
follow Fabio Carisio Gospa News director on Twitter
follow Gospa News on Telegram
MAIN SOURCES
Moderna AWARE that mRNA Jabs cause CANCER due to DNA Fragments. Malone Unveils Patent
Un pensiero su “Diabolical Molecule inside mRNA Vaccines generates Harmful Proteins as Killer Prions, “Brain-Eating Amoeba”. Explosive Study by prof. Perez (Montagnier Foundation)”