The Origin of Life Upon Earth

Deoxyribonucleic acid (DNA) is most likely not the first building block of life because of its complicated double helix pattern. Ribonucleic acid (RNA) is also statistically unlikely because although it is only half as complex as deoxyribonucleic acid being that it does not resemble a double helix structure, but rather a single helix structure, it would have required 5 specific sugar molecules to spontaneously bind together, one by one, in a very specific order. Threose nucleic acid (TNA) however, would only require 4 identical simple sugar molecules to spontaneously, come together. This is theoretically the most probable candidate for being the first spark of life. Threose nucleic acid can easily base pair and exchange genetic information with ribonucleic acid making it the best blueprint which would have shown up long before the complex cellular machinery, which is found within all living cells today

How Plants Produce Food Via Photosynthesis

If a leaf is magnified 1000x, green bacteria like structures can be observed, referred to as “chloroplasts,” which are packed into virtually every cell of a plant. These chloroplasts behave like bacteria, retaining their own deoxyribonucleic acid, and are only 5000ths of 1 millimeter (0.005 millimeters or 5 micrometers) in diameter. It is inside chloroplasts that photosynthesis occurs. Photons, which are tiny and rapid moving particles of electromagnetic energy (e.g. rays of light), are harvested upon the surface of the plant’s leaves, where they then enter the plant’s cells and are absorbed by the light harvesting complex located within the chloroplasts themselves. It is here that the photon is leveraged to drive the photolysis reaction, which is to split a water molecule and release oxygen, electrons, and hydrogen ions, fueling the energy transfer mechanisms that ultimately convert carbon dioxide into sugars for the plant’s growth and survival

The Argument Against Stem Cell Research and Why This Will No Longer be a Problem in the Future

The reason stem cell research is controversial for some is because it is viewed as damaging and harvesting from one life to help another. This argument may be obsolete in the future as scientists are now discovering ways to create stem cells from cells within the body (e.g. skin cells etc.). The traditional method to create a stem cell was to take a skin cell, remove the deoxyribonucleic acid from its nucleus, placing it into an egg which does not have deoxyribonucleic acid but is capable of changing deoxyribonucleic acid, turning it into a stem cell which has the patients genome ascribed unto it. The new method involves placing 4 genes into the nucleus of the skin cell and allowing time to pass, as the genes reorganize the deoxyribonucleic acid so that it begins to appear as stem cell deoxyribonucleic acid, which changes the skin cell and causes it to shrink, losing its outside, converting it into an embryonic stem cell with the only difference between this method and traditional embryonic stem cell creation method being that this technique contains the deoxyribonucleic acid of the patient it is being inserted into. The 4 genes inserted into the cell create 4 proteins which exist naturally within an egg. These proteins trigger the skin cell deoxyribonucleic acid to arrange itself identically to how it would within an embryonic stem cell. Scientists refer to this type of cell as “induced pluripotent stem cells”, commonly abbreviated as “IPS cells”. Ideally, scientists want induced pluripotent stem cells to function identically to natural embryonic stem cells, avoiding the creation of unwanted cells which can lead to cancer. Researchers have discovered that some laboratory created stem cells fail to carry out the task provided and worse yet, some cause cancer to develop. Scientists are currently pursuing 2 paths to alleviate this problem, the first being the attempt to develop induced pluripotent stem cells which function identically to natural embryonic stem cells and the second being to create a system to recognize which induced pluripotent stem cells will fail in an effort to exclude these cells from being inserted into the human body

A Revolutionary Breakthrough in Oncology Treatment

Cancer kills 9,000,000 (9 million) people each year and despite having searched for centuries, a cure has yet to be discovered by scientists. At the center of the immune system is the T cell, a type of leukocyte which respond against bacterial and viral infections alike in an effort to keep their host healthy and alive. T cells determine between threatening and non-threatening foreign and non-foreign bodies within a host by leveraging a molecule upon the surface of all cells referred to as the “T cell receptor”. Jim Allison was the first person to successfully isolate and purify the molecule which recognizes this lock and key model for infectious disease, auto-immune disease, and other innocuous substances within the body be they foreign or internally created. In 1987, French scientist Pierre Golstein and his team discovered a new protein upon the surface of T cells which he named “CTLA-4”. To study CTLA-4 in laboratory rats, Allison had to build and design a rat antibody, a Y shaped protein which would trigger a reaction by CTLA-4. Cancers are mutations and should in theory be visible to the immune system, which is why the scientific community has struggled with the paradox of why tumors go undetected by the immune system for decades. There is no discernible reason as to why the immune system can recognize and resist influenza or any other foreign or domestic body but not cancer. Allison theorized that tumors have evolved an ability to fool the immune system, engaging CTLA-4 which turns on the T cells response to halt its search and destroy measures. Allison hypothesized that if he inserted a Y shaped antibody to block the gap in between the tumor and T cells, the tumor would no longer have its ability to hide, a trait which has been evolved by tumor cells over hundreds of millions of years. This would allow the T cell to infiltrate, attack from within the tumor, shrink, and ultimately kill the growth. Allison spent the next decade trying to turn this revolutionary breakthrough discovery into a medication which could be provided to cancer patients. Allison found Alan Korman, a scientist creating medications for auto-immune disease which provided him with the expert he required to turn this idea into a reality. Korman was tasked with taking the CTLA-4 antibody which Allison and partner Max Krummell developed for laboratory rats, and turn it into a medication which could safely work within human beings with this medication subsequently being named “Ipilimumab” (pronounced “ipi-lim-ooh-mab”). Korman ended up collaborating with a friend from graduate school, Nils Lonberg to accomplish this task. Ipilimumab consists of an intramuscular injection into the leg and a 90 minute intravenous medication drip in comparison to chemotherapy and radiation therapy which take months of treatment to complete and have devastating effects upon overall health as both bad and good tissue are destroyed in an effort to eradicate all tumor cells. Allison’s work with laboratory rats demonstrated that with the help of this newly developed antibody, T cells gained the ability enter into tumors and expand their size in an effort to destroy them from the inside out. This means that the fact that tumors grow initially upon administration is a positive marker and indicative of the medication working as it demonstrates successful infiltration of the tumor cells themselves. Patients often report feeling better after a few treatment sessions, sometimes even a single session, despite computer tomography scans demonstrating that their tumors are growing larger, which under normal circumstances would make a patient feel worse. Some patients even noted increased improvement after having stopped the Ipilimumab treatment, with no further therapy required. On March 25, 2011, the U.S. Food and Drug Administration released approval for Ipilimumab. Ipilimumab and its successors have treated nearly 1,000,000 (1 million) patients worldwide with many of these patients achieving permanent remission which is essentially the definition of having been cured of cancer. Although these medications do not work in every single case, they have definitively demonstrated to be a miracle medication for hundreds of thousands of people thus far. After completing this revolutionary discovery, Allison was awarded the Nobel Prize in Medicine in 2018 for his series of discoveries related to T cells and their ability to halt cancer in its progression in perpetuity

The Etymology of “Matter Plasma” and “Blood Plasma”

The term “plasma” is derived from the ancient Greek term “plassein” which means to “shape or mold something”. Plasma related to physics, specifically matter which has had its electrons separated from the rest of its atoms, forcing it to become an ion, more specifically a mixture of free floating electrons and ions, was first identified by British chemist and physicist Sir William Crookes in 1879 using cathode ray tubes. Crookes referred to this discovery initially as “radiant matter” but it became known as “plasma” in 1928 because of American chemist Irving Langmuir. Langmuir was exploring ionized gases, gases which were subjected to strong electrical fields to remove electrons from their orbital shells. Langmuir used the analogy of blood to explain this phenomena, with the ions representative of corpuscles and the remaining gas thought of as clear liquid. Blood is similar to plasma in that it is primarily comprised of 2 components which include its clear liquid and the corpuscles/cells entrapped within this fluid. This clear liquid was named “plasma” by Czech physiologist Johannes Purkinje In 1927. The definition of matter plasma and blood plasma however have absolutely nothing to do with eachother physically, aside from the fact that two different scientists had the idea to use the same term at approximately the same time. It is believed that these two scientists based their name upon the ancient Greek definition of the term “plasma”

The Fallout of the Chernobyl, Ukraine Nuclear Meltdown

In 1986, the world’s worst nuclear accident occurred, when the Chernobyl nuclear reactor within the Ukrainian Soviet Socialist Republic exploded releasing 400x as much radiation as the nuclear weaponry which was dropped upon Hiroshima, Japan in 1945 towards the end of World War II. The most dangerous classification of radiation which can be emitted after a nuclear meltdown or detonation of a nuclear atomic bomb are gamma rays, which like x-rays are made up of high energy photons which can travel long distances. Most gamma rays pass straight through an observer, but not all do and these free particles cause fragmentation of deoxyribonucleic acid and damage at the cellular level which can ultimately lead to cancer and subsequently death

Sterilization Using Ultraviolet Radiation

Ultraviolet radiation disrupts the chemical bonds which hold bacteria and viruses together. Ultraviolet radiation is able to kill the cell and ensures whatever material is exposed afterwards becomes sterile. The longer an organism is exposed to ultraviolet radiation, the less likely it is to have any microbes alive upon it. Hospitals and various industries utilize this method of sterilization to ensure their equipment and environment is as free of microorganisms as possible