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      <title>Nate&#39;s Biology Standards by Stitt, Nate</title>
      <link>https://padlet.com/stittn23/17t2nucejpr32cgl</link>
      <description>2021-2022 school year</description>
      <language>en-us</language>
      <pubDate>2022-02-22 09:03:22 UTC</pubDate>
      <lastBuildDate>2025-11-22 16:37:31 UTC</lastBuildDate>
      <webMaster>hello@padlet.com</webMaster>
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         <title>S.15 (Conclusions)</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060177032</link>
         <description><![CDATA[<div>Attached, you'll find my data, goals for this conclusion, and notes concerning the lab. Below, you'll find my initial assessment.</div><div>&nbsp;</div><div>CONCLUSION:</div><div>(CLAIM AND INTRODUCTION): First, a hypothesis: as the agar cube decreases in size, its diffusion rate will increase and vice versa; thus, there is a correlation between surface area and diffusion rate. Next, let's clarify what the agar cube actually represents in this experiment:&nbsp; the outer layer of the cell membrane (the cytoplasm). Throughout this experiment, I aimed to determine how the agar cube's size impacted its diffusion rate. But what do these terms actually mean? Writ large, this experiment concerns how molecules are even able to pass through the cell membrane. For these molecules and more to pass through, the outer layer cell membrane has to diffuse – spread out or widen. Thus, diffusion can be defined as the spread of the outer layer of the cell membrane becoming wider. This description is measured by the percent of diffusion in our data table. For added analysis, my hypothesis for why cells are limited in size is because their membrane can only diffuse to a certain extent – meaning much larger molecules such as Glucose are unable to pass through the cell membrane as the membrane is unable to diffuse to the extent necessary that would permit this occurrence.</div><div>&nbsp;</div><div>(EVIDENCE): To begin, I will analyze the data my group came up with before analyzing that of the class through the lens of qualitative and quantitative reasoning. Qualitatively, my group and I noticed the color of the agar cube as more vinegar was added to its surface. We questioned: what does this signify? The agar cube's color change signified how much diffusion has occurred. From a molecular, chemical standpoint, when the agar cube was placed into vinegar, the agar cube's color changed as the hydrogen ions transferred from the vinegar to the cube. So, when an agar cube had a relatively small surface area was dipped in vinegar, more of its area changed colors as more of the area diffused. Quantitatively, both my group's data and that of the whole class back this hypothesis up. For my group's data, the percent of diffusion for the agar cube with the smallest surface area is nearly 38% greater than that of the agar cube with the largest surface area. Additionally, for the data for the whole class – taking Viraja and Chancey's data as an example – the comparative increase in the percent of diffusion between the largest and smallest agar cube is 21%. Finally, the time that it takes for a larger agar cube to diffuse appears to be longer as well; look toward Viraja and Chancey's data once again for a class comparative, wherein the 3x3 cube took 420 seconds, while the 1x1 cube took only 360 seconds.</div><div>&nbsp;</div><div>(REASONING): The explanation for why the agar cube's diffusion rate increases when its surface area is smaller it has a smaller surface area to volume ratio. Note, as pictured above, volume is measured in mm cubed while surface area is measured in millimeters squared – the key difference: cubed vs. squared. The volume appears to become larger at a more rapid rate than surface area because its measurement multiplied by itself three times means the volume will increase more than surface area, as the surface area is only multiplied by itself twice. Connecting back to the core theme of the experiment concerning how molecules pass through the membrane, we can now conclude that increased amounts of volume and decreased amounts of surface area means that diffusion appears to be less effective and take more time. For molecules to pass through the membrane, the membrane has to diffuse and spread out. Thus, since bigger cubes diffuse slower than smaller ones and at a less efficacious rate, another conclusion we can make chemically is that some larger molecules are unable to pass through the membrane.</div>]]></description>
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         <pubDate>2022-02-22 09:09:22 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060177032</guid>
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         <title>S.15 Data (Part 2)</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060184398</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-02-22 09:14:41 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060184398</guid>
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         <title>S.15 Data (Part 1)</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060184912</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-02-22 09:15:05 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060184912</guid>
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         <title>S.9 - Gene Expression</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060194548</link>
         <description><![CDATA[<div>This is an annotation for standard 9: Gene Expression. Please look to both the writing below and my protein project (emailed – on 11/1, video format) to assess this standard.&nbsp;</div><div>&nbsp;</div><div>So – what are transcription and translation? Simply put, transcription describes when DNA is copied into RNA, while translation is making that copy into information by turning amino acids into proteins. First, let's do a deeper dive into transcription. Two strands of DNA are held together by hydrogen bonds. Transcription describes the process of when the DNA is twisted, and the RNA comes to match the strands of the DNA. The first thing that happens in transcription is the DNA strands must be split apart. The protein that performs transcription is RNA polymerase because it is making RNA. RNA polymerase is an enzyme (something that starts a chemical reaction) that opens up this DNA with two strands with the goal that one strand of the uncovered nucleotides can be basically utilized as baseline (the base pair) for the synthesis of RNA. RNA Polymerase works because of chemical reactions. This "base pair" begins to exist once a ribonucleoside triphosphate (the nucleotide that is exposed) matches with the DNA. Notably, the template strand is the original, base, hard copy. The "A"s, "T"s, "G"s, and "C"s determine if they match. Also, “T”s are only in DNA, while “U”s are only in RNA. "A" pairs with "U" and "T" while "G" pairs with "C". Finally, in reality, As can try to fit with Gs but don’t fit chemically and so they fit with their pair. Next in the process, a chemical reaction takes place wherein electron-rich oxygen will attack an electron-poor molecule to create a new bond. After, the base pair shifts over 1 letter (as illustrated in the Concord Lab) to position the hydroxyl group closer to where the new nucleotide, so these chemical reactions can continue as new "A"s, "T"s, "G"s, or "C"s, match, and the process continues. Next, what is translation? Translation makes these new copies of RNA into actual information by turning amino acids into proteins. The ribosome is the machine that performs the translation. The ribosome will read the sequence of an mRNA to first get the message that it can then translate into amino acids. mRNA stands for messenger RNA – it is a codon, meaning triplets on mRNA that specify an amino acid and give instructions to the ribosome; I.e. adenine or guanine. Chemically speaking, the ribosome will translate each codon once tRNA – the transferer – will transfer amino acids to the ribosome. tRNA is an anticodon, which is complementary to codons. A complimentary sequence then occurs once the codons and anti-codons fit together. (and these nucleic acid sequences match base pairs; the As match with Ts, etc.) But how do the ribosome and tRNA “know” what amino acid corresponds with that DNA sequence? Its chemical structure which determines if they fit. Finally, polypeptides, which are the protein chains that exist after translation, are simply the physical manifestations of the information just transcribed and translated. They are the proteins that exist from amino acids through the process of translation. When there a tRNA visualizes a "stop codon" – which has matches of UAG, UGA, or UAA, and this stop codon will terminate the process of translation. Attached, find a visual representation of the process I just described.</div>]]></description>
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         <pubDate>2022-02-22 09:21:55 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060194548</guid>
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         <title>S.9 Visual - Gene Expression</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060195082</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-02-22 09:22:18 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060195082</guid>
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         <title>S.7 – Cell Signaling</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060199214</link>
         <description><![CDATA[<div>Reception – ok so first let me describe – how does a cell receive the GPCR signaling molecule?<br><br>Let’s first dissect what the term GPCR even means. It means you have a G protein, specifically a Heterotrimeric G-protein, that is made up of alpha, beta, and gamma subunits. Note- hetero-TRI-metric. Basically, these 3 subunits make up one large G protein, and that G protein is coupled with receptors. This occurs within the plasma membrane which is in the cell membrane. Here, you have ligands that come over to the GPCR&nbsp; receptor. And once they find their complementary receptor, it will fit in like a puzzle. THIS MEANS: once another ligand finds your GPCR, then the ligand attaches to its desired GPCR receptor. There are many different types of cells to carry out the GPCR's functions. Some examples include hormones, neurotransmitters, proteins, peptides, or even lipids.<br><br>Transduction – ok so next I’ll explain how the signal is passed along.<br><br>Basically, the alpha subunit of the G protein now bonds with either GDP or GTP, depending on whether the protein is active or inactive. GDP – meaning di, two proteins– is inactive – while GTP – tri, meaning three proteins and – is active. The GDP, which is the inactive part, will couple with the alpha subunit that binds to the GPCR to start signaling.&nbsp;<br><br>Now – what are some processes that occur to further the signal.<br><br>The G protein, now bound with the GPCR, regulates your adenylyl-cyclase – an enzyme that converts ATP (Adenosine triphosphate) energy into cAMP responses (cyclic AMP). These cAMP responses are the signal’s secondary messenger, which amplifies the signal. That’s why this part of the process is called signal amplification. So these messages that cAMP responses further then connect to other parts within the plasma membrane. These sections get closer and closer to the desired receptor. In our model, we used the example of Orexin Receptors – which are GPCRs that receive orexin, which is a neuropeptide that regulates things like sleep, wakefulness, and hunger. So in this hypothetical let’s say that the message one’s body signals is hunger. On a chemical, molecular level —The cAMP responses would then activate neurons and release ions to further their scope in order to get closer and closer to the point where the signal needs to go for the response to happen. that is the hypothalamus, which is one of the main parts of the brain that controls hormones. the final step in this transduction process is one in which a depolarization spike occurs. basically the electronegativity - specifically the accumulated difference in polarity on the other side of the cell - causes a big spike, meaning no more Na+ can scoot around the cell. the activation gate, which basically has been allowing all of these processes to occur, closes. at this point, there are already a bunch of neurons that have received the hunger signal, but one of them close to the hypothalamus sends the signal directly to it.<br><br>Finally, what does the cellular response look like? the neuron with the orexin receptor continues to relay the hunger memo along to the hypothalamus. now that the hypothalamus has received the message, your body tells you you are hungry!&nbsp;<br><br>but when you begin to eat a lot, your body becomes full. the only way you are able to know this is if you stop this process and shut off the signal from the orexin receptor. to do this, the active GTP will take over the inactive GDP. the subunits come together and the active part, the GTP, has now shut the hunger signal that the orexin receptor relays to the hypothalamus down.&nbsp;</div>]]></description>
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         <pubDate>2022-02-22 09:25:11 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060199214</guid>
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         <title>PDF of Infographic and Annotations</title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060214549</link>
         <description><![CDATA[<div>My reassessment of these two standards is below, but for sake of including my original work on this padlet, here is my initial PDF from first semester.</div>]]></description>
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         <pubDate>2022-02-22 09:34:46 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060214549</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060222969</link>
         <description><![CDATA[<div>Above, I stated: "For these molecules and more to pass through, the outer layer cell membrane has to diffuse – spread out or widen. Thus, diffusion can be defined as the spread of the outer layer of the cell membrane becomes wider. This description is measured by the percent of diffusion in our data table."&nbsp;<br><br>However, diffusion does not refer to the phospholipids of the bilayer membrane, as I assumed above. Rather, diffusion refers to molecules moving through the membrane and then into the cell. This means that my above description would not follow what diffusion truly looks like. So, an amended version would explain that diffusion could be defined as the process for how molecules move through the membrane and into the cell depending on the concentration of molecules that exist at a given point.<br><br>&nbsp;</div>]]></description>
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         <pubDate>2022-02-22 09:40:24 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2060222969</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2078404114</link>
         <description><![CDATA[<div>In this standard, I aim to describe and justify the process of scientific research, and communicate about scientific topics in a level-appropriate way. I will use the Cell Cycle project to illustrate this standard. In my study of glias, gliomas, and brain cancer for the Cell Cycle project, I utilized scientific research and made notes for the project. Attached, you will find the highlighted and annotated PDF of published research from The Hidalgo Lab that demonstrates my knowledge and ability to conduct scientific research.</div>]]></description>
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         <pubDate>2022-03-04 18:10:21 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2078404114</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2078458515</link>
         <description><![CDATA[]]></description>
         <enclosure url="https://padlet-uploads.storage.googleapis.com/1585740864/d946ec2ae90fec175b1e84755fe97bb2/Regeneration_and_Glia.pdf" />
         <pubDate>2022-03-04 18:46:00 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2078458515</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2080167218</link>
         <description><![CDATA[<div>In this standard, I aim to describe in general terms how the information in a gene is stored, replicated, and transmitted to daughter cells.<br><br>Meiosis simply describes a cycle where one cell alone will isolate itself and divide twice to create four sex cells with fewer genes. The glial cell needs to make copies of its genetic materials in order to start the process of cellular division and reproduce its daughter cells. This means it chemically must create more DNA cells to be copied (before they are actually divided). Glial cells – which are eukaryotic because they have a nucleus – wrap their DNA to create chromosomes into bundles. These form tight chromosomes, which have two chromatids. (THIS IS HOW THE GENE IS STORED) The chromatids enter the new daughter cells that form after they’re divided. This means the glial cells, for example, have these chromatids. Chemically, chromatids separate because of enzymes, which speed up the process of chemical reactions. A chemical called cohesin, which previously kept the sister chromatids connected, now is being used to separate the chromatids. (THIS IS HOW THE GENE IS REPLICATED). After this happens, gametes are produced. Gametes are basically just sex cells. They have unique alleles, which chemically are simply changes to a gene strand. These gametes come together when they fertilize – X and Y chromosomes fertilize to creating a male sex, while XX makes a female sex offspring. (THIS IS HOW THE GENE IS REPLICATED). Diploid cells have 2 full sets of chromosomes, while haploids have 1. These cells are altered during meiosis – just look toward how the glial cells will condense and separate. That’s how cells separate during meiosis and inherit new genes!</div>]]></description>
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         <pubDate>2022-03-06 18:43:40 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2080167218</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2080167318</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-03-06 18:43:49 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2080167318</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2080195967</link>
         <description><![CDATA[<div>In this standard, I aim to contrast the features that distinguish viruses, bacterial cells, and eukaryotic cells from each other. The portfolio piece that coincides with this standard is the cell cycle project.<br><br>First, what is a virus? A virus is simply a tiny, infectious go-getter that aims to take over a host cell. A virus is non-cellular.<br><br>Second, what is bacteria? Bacteria are just germs. You can't see them, but they're everywhere. They can act positively or negatively and can work alongside enzymes (which is what kick-starts chemical reactions).<br><br>Third, what is the difference between prokaryotes and eukaryotes? In contrast with viruses and bacteria, prokaryotes and eukaryotes are cellular. They have cells. However, the difference between the two is that prokaryotes are cells that lack a nucleus, while eukaryotes have a nucleus.<br><br>Applying the knowledge I obtained from the portfolio project, Gliomas – which are the most common form of brain tumors – are not cells. It is possible (and probable) that bacteria grows on brain tumors. Still, gliomas are not viruses as they are created when the glia cells grow far-too-quickly. Glia cells are made of eukaryotic cells, not prokaryotic cells. At the same time, there are many other viruses that can infect the brain – tumors simply aren't one of them.</div>]]></description>
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         <pubDate>2022-03-06 19:24:25 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2080195967</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2183186299</link>
         <description><![CDATA[<div>In this standard, I aim to address the theory of evolution, and cite evidence that it is an ongoing process affecting our daily lives. I will contextualize this process on a deeper chemical level by discussing concepts of energy flow during metabolism. Additionally, I will explain how an enzyme increases the rate of a biochemical reaction in terms of thermodynamics, kinetics, and molecular interactions – and what this means for the energy flow process + evolution. The piece I am citing for these two standards is the "Energy and Metabolism" slideshow – specifically the first video on exercise (and rats) in slide two. I know this is a lot, but these three standards feel specifically interconnected to me. Using each as a mechanism to contextualize another has allowed me to better understand these concepts writ large.</div>]]></description>
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         <pubDate>2022-05-13 16:59:33 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2183186299</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2184091405</link>
         <description><![CDATA[<div>First, the theory of evolution describes how characteristics – whether external or internal – change in a given organism over a long period of time. Evolution is driven by mutation, a random process. Note that some traits are passed down to the next generation, but the initial process is random. Mutation is the changing of letters in genetic “code” – the building material, and it happens when mistakes are made in the genetic material. So, all of this genetic mutation occurs within genetic material such as DNA/RNA (but is most prominent in RNA). In the genetic code, nucleotides are represented in triplets on a chemical level. For example, ACU/ACA/AAU. Notably, there is a relationship between these triplets and PROTEINS – as proteins are also part of a sequence, meaning they have an “alphabet” too. This process eventually looks like changes in rats' genetic components, such as a stronger sense of smell, which I witnessed in the Energy and Metabolism slideshow. The process of energy flow during metabolism occurs by the movement of electrons. This broadly looks like enzymes continuously operating to spread "information." Enzymes primarily act as chemical catalysts for change – and they primarily do this by decreasing the energy of a given reaction. They tighten around a substrate (a reactant) on a chemical level, and this process minimizes the energy needed to activate a reaction. Though enzymes are catalysts for chemical change, they actually do not affect thermodynamics. While enzymes may speed up a chemical reaction, they don't change equilibrium concentrations. Enzyme kinetics, however, which is the reaction rate of a given enzyme, certainly changes based on the strength of the enzyme's role in metabolism. In this process of energy flow, one should expect an enzyme to increase the rate of kinetics, given that they are speeding up chemical reactions. Going back to the energy flow process, a flux of electrons is then sent down (as enzymes continue to operate) across the membrane after an organism consumes food. Large proteins pass these electrons down, resulting in an electrical current. This current drives expansion – these proteins pump protons to charge them, resulting in practical storage of protons.&nbsp; This is a generator of energy for storage in a cell (all of this is called ATP synthase). You can think of this like a turbine; it just keeps going - and primarily occurs in the mitochondria, which is the "powerhouse" of the cell. All of this continues to occur (practically all the time) in organisms because enzymes speed up chemical reactions, forcing an increase in molecular reactions and continuing this cycle that drives energy. This process then relates to evolution because energy flow informs the evolutionary process, given that (a) the mitochondria is likely to have played at least some role in shaping the evolution of eukaryotic cells because, over time, its process of energy transfer may have changed components of the genome and (b) changes to the genome can only occur when an organism has energy and can live and reproduce for long periods of time. In daily life, evolution manifests itself by protecting organisms from what their ancestors may have faced, like deadly diseases – or even circumstances as simple as adapting to proximity to the equator.</div>]]></description>
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         <pubDate>2022-05-14 20:53:51 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2184091405</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2185786201</link>
         <description><![CDATA[]]></description>
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         <pubDate>2022-05-16 14:10:02 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2185786201</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2188019507</link>
         <description><![CDATA[<div>S.1 Reassessment) Initially, I did not cover all four macromolecules including the chemistry of the molecules and some of the details of how they are used in biological contexts. Though I accomplished this for phospholipids in my discussion of polarity and why they would form bilayers in water, I failed to explain how Proteins, Nucleic Acids, and Carbohydrates are also used. So, I'll do that here! To begin, in the context of the social construct of beauty – specifically with plastic surgery – proteins are vital in ensuring that tissue is healed. This would look like scarred tissue after plastic surgery (a rhinoplasty for example) that eventually heals because of proteins. Chemically, this occurs because proteins transport substances/nutrients through diffusion. Passive diffusion occurs when the transport of these molecules is from a low to high concentration (think of a food color droplet going into water), while active diffusion is vice versa (high to low). Next, nucleic acids store genetic information (DNA and RNA). On a broader scale, these are the building blocks of the body – they tell the body when/how to create the aforementioned proteins. This in turn allows for the proteins to accomplish their necessary functions and provides nutrients to allow tissue to heal in the first place. Chemically, DNA is made up of nucleotides which create strands – this is where the concept of As, Ts, Gs, and Cs play in, as they match with one another to create these strands, which inform bodily functions. Finally, carbohydrates give the body glucose. Glucose is eventually converted into energy through the process of cellular respiration in which glucose and O2 form ATP (Adenosine triphosphate, stored in the mitochondria). This is a vital function for the body not just for the healing process, but before that and throughout a given human's life. For instance, Carbohydrates are a necessary macromolecule before a patient goes under anesthesia or even simply at a doctor's visit, because the body practically always requires energy.</div><div><br></div>]]></description>
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         <pubDate>2022-05-17 17:15:21 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2188019507</guid>
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         <title></title>
         <author>stittn23</author>
         <link>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2188028039</link>
         <description><![CDATA[<div>S.5 Reassessment) Initially, I falsely described a membrane made of cells as the phospholipid bilayer. Though I addressed the polarity aspect of this standard, I will continue to address the importance of channels in the membrane. Broadly, I will address what can and cannot move across the membrane and why. I'll contextualize this question by using the example of compounds that are touted with beauty products. To begin, primarily simple molecules can move across the membrane. Common examples include O2, CO2, and H20. These molecules accomplish this through diffusion. There is passive diffusion, in which molecules move from a low to high concentration, and there is active diffusion, in which molecules move from a high to low concentration. These molecules can move across the membrane because they are nonpolar (no positive/negative poles). Chemically, this makes sense because smaller, simpler, nonpolar compounds can easily travel through the nonpolar part of the phospholipid bilayer because of their size/shape. On the contrary, larger, polar molecules could not (at least without the assistance of transport proteins). These transport proteins facilitate the process of diffusion for larger and polar molecules because they can create openings/gaps, moving against the concentration gradient. In the context of my portfolio piece, this would mean that a compound touted in beauty products would be unlikely to be able to move across the membrane by itself. One could assume that these compounds are comparatively larger and polar. The more likely thing to occur in a beauty product is that it has a carrier to allow molecules to cross the membrane. On the contrary, cleaner compounds such as hyaluronic acid (which is known to heal tissue) might more easily pass through the cell membrane. Though it is polar, a transport protein could help move it across the membrane. It is mainly located in the extra-cellular matrix Hylauronic acid has receptors, which regulate cell adhesion and adversely healing of the cell. Another effect is migration - new cells need to migrate to where they are supposed to be. (A lot of this ties back to cell signaling, but that just notes the intersection of these standards). Given that "the synthesis of HA [hylauronic acid] increases during tissue injury and wound healing," (https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583886/#:~:text=Biological%20function%20of%20HA&amp;text=The%20synthesis%20of%20HA%20increases,49%2C50%20and%20epithelial%20cells), it is fair to assume that the receptors of hyaluronic acid aid it in passing through the membrane even as a polar compound.</div>]]></description>
         <enclosure url="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583886/#:~:text=Biological%20function%20of%20HA&amp;text=The%20synthesis%20of%20HA%20increases,49%2C50%20and%20epithelial%20cells" />
         <pubDate>2022-05-17 17:20:14 UTC</pubDate>
         <guid>https://padlet.com/stittn23/17t2nucejpr32cgl/wish/2188028039</guid>
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