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Human C-Reactive Protein 1GNH

spinqualitylabelsall models Caption for this structure Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D This is a default text for your page MillerSandbox1. Click above on edit this page to modify. Be careful with the < and > signs. You may include any references to papers as in: the use of JSmol in Proteopedia or to the article describing Jmol to the rescue. Background Throughout the medical field, the Human C-Reactive Protein (CRP) has been used to clinically determine whether or not there is an infection, tissue injury, or an inflammatory response occurring within the body. Thus, CRP is a major acute-phase protein, in which its concentration can reach levels upwards of 10+mg/L (<ref>ref name="Evolution of CRP" Pathak A and Agrawal A (2019) Evolution of C-Reactive Protein. Front. Immunol. 10:943. doi: 10.3389/fimmu.2019.00943). In comparison, normal CRP levels within the human body are referenced to be estimated at 0.8mg/L depending on the subject. In a pathophysiological sense, CRP has been researched to be a "significant predictor of future cardiac episodes" (Boncler et al.). With that, CRP is determined to play a specific role in both physiological and pathophysiological aspects within the human body. Structure CRP has a mass of 23kDa per subunit with 206 amino acid residues because it is a pentameric protein, which means it is "composed of five identical noncovalently bound subunits" (Pathak and Agrawal 6). Functionally, CRP will "bind to [phosphocholine] PCh in a Ca - dependent manner" (Pathak and Agrawal); moreover, CRP has five binding sites for PCh, one on each subunit (Pathak and Agrawal). Some of the amino acids that are directly present in the binding sites include, Glu81, Phe66, and Thr76. The Glu81 forms hydrogen bonds with the nitrogen atom that is within the choline group of the PCh, "Phe66 interacts with three methyl groups of choline" (Pathak and Agrawal 6), and the Thr76 is a crucial aspect in opening the binding site to an appropriate size for the PCh (Pathak and Agrawal 6). Furthermore, PCh's phosphate group is interactive with two Ca2+ molecules that are bound to the CRP (Pathak and Agrawal 6). The Ca2+ is the bound ligand to the C-reactive protein with two calcium ions per protomer. Structurally, each subunit is configured around a central pore and is arranged in a "characteristic 'lectin fold' with a with a two layered beta-sheet," and they lie within the PCh binding site facing the "recognition face of the CRP molecule" (Pathak and Agrawal). Regarding the ligand, the calcium ions are crucial for the stability of binding the ligand to the molecule. Moreover, CRP is primarily synthesized within liver hepatocytes; however, the protein can also be synthesized by smooth muscle cells, macrophages, endothelial cells, lymphocytes, and adipocytes, which are other types of cells within the body (Pathak and Agrawal). Its pentameric structure is "first synthesized as a monomer and then assembled into the pentamer in the endoplasmic reticulum of the source cell" (Pathak and Agrawal). CRP is then retained in the endoplasmic reticulum within hepatocytes and is bound to two carboxylesterases, but while it is in the non-inflammatory state, or resting state, it is slowly released from the endoplasmic reticulum (Pathak and Agrawal). Additionally, "following an increase in inflammatory cytokine levels, the binding of CRP to the carboxylesterases decreases, and the CRP is secreted rapidly" (Pathak and Agrawal). This stimulation is only in response to pro-inflammatory cytokines. The Human C-reactive protein can also be "irreversibly dissociated into termed monomeric CRP where the free subunits are found at high concentrations of urea and in high temperature with the absence of calcium" (Pathak and Agrawal). This monomeric isoform of CRP is termed mCRP, whereas the pentameric is termed nCRP. Each isoform of CRP is distinguished to have their own biological functions to an inflammatory response (Pathak and Agrawal). One study concluded and "provided evidence that nCRP suppresses the adherence of platelets to neutrophils, whereas mCRP enhances these interactions" within an inflammatory response (Pathak and Agrawal). During the inflammatory response within the body, there is a signaling process where the body calls for protection against the abnormality. Thus, this difference in the two isoforms can be related to this process and their binding to the specific types of "Fcgamma" receptors (Pathak and Agrawal). Explaining this difference, "the mCRP isoform utilizes the low-affinity immune complex binding immunoglobulin G (IgG) receptor called (CD16B) on neutrophils and (CD16a) on monocytes, while nCRP bind to the low-affinity IgG receptor (CD32) (Pathak and Agrawal). Thus, the two isoforms have their own binding processes during the signal process of an inflammatory response. In general, the "nCRP isoform is more directed towards an anti-inflammatory response, whereas the mCRP isoform is particularly involved in pro-inflammatory responses (Pathak and Agrawal). However, there are "antibodies that are not commercially available to date [to detect mCRP levels], so few laboratories can conduct studies investigating the mCRP isoform" (Pathak and Agrawal). Thus, leading to the indication that each isoform is crucial to different abnormalities within the human body. Medical Applications During the times of COVID-19, which appeared in the year 2020, pneumonia is one of the biggest worries a person could develop while having the upper respiratory infection. The most common type of bacteria that causes an upper respiratory infection is the Streptococcus pneumoniae bacterium, and it is also the most common culprit of septicemia and meningitis (Structure and function). While contracting one of these infections, the CRP will bind to the bacteria through the "Ca2+ dependent reactions with PCh residues" on the bacterial cell walls (Structure and function). Structurally, PCh is widely distributed inside and outside of pathogens and in the cellular membranes, which allows CRP to recognize a wide range of pathogenic targets and damaged host cells. This reaction raises the CRP levels within the serum of human blood, allowing for a laboratory test to detect the elevated levels of CRP, indicating that an infection or inflammatory response is occurring within the body. Human C-reactive protein plays a significant role in the acute phase of defense against pathogens. CRP will specifically bind to the damaged membranes of host cells where there is "an increased proportion of Lysophospholipid (Thompson et. al). The ability of CRP to contribute to the innate immunity within the body allows for it also to prevent autoimmunity (Thompson et. al). It has also been discovered that CRP is a crucial indicator in the complications or outcomes of an individual after suffering a myocardial infarction (heart attack) where "CRP will deposit into the infarcted tissue, and it activates complement" (Thompson et. al). This response triggers the body's "classical complement pathway of innate immunity by activating C1q" (Pathak and Agrawal). The activation of this innate immunity allows for the body to start the healing process within the localized area. However, CRP levels vary amongst a wide variety of infections or injuries. CRP levels can diminish over 18-20 hours after the stimuli has ended, and the levels can continue to increase if there is a more serious underlying condition such as progressive cancer (Pathak and Agrawal). There are also many more factors that alter the baseline levels of CRP within the body that include "age, gender, smoking status, weight, blood pressure, and lipid levels (Pathak and Agrawal). Baseline CRP levels of an individual can be found around a level of 0.8mg/L in a healthy Caucasian, "but this baseline can vary greatly in individuals due to [the] other factors, [also] including polymorphisms in the CRP gene" (Pathak and Agrawal). Although polymorphisms have been found with the CRP gene, "there are no allelic variations or genetic deficiencies discovered for this gene" (Pathak and Agrawal). A study was conducted with twins that "showed significant heritable components in [the] baseline CRP values that are independent of age and body mass index" (Pathak and Agrawal). The study concluded that the CRP levels are roughly 35-40% heritable (Pathak and Agrawal). It is known that CRP levels are elevated due to disease, so the levels cannot be directly reduced through the administration of drugs, but rather, by directly treating the underlying medical condition. Furthermore, it is widely known that the CRP protein is crucial in the determination of the pathophysiology of the human body. There are multiple benefits for its use in determining different diseases that are occurring within the body. For example, the determination of elevated CRP levels can indicate other types of infections, such as appendicitis, cholecystitis, and pancreatitis. On the other hand, the tests have to be conducted within a specific period once the clinically indicated symptoms have occurred; otherwise, the results will not show any of the biological markers, and the CRP levels will decrease over 12-18 hours. Conclusion In conclusion, Human C-reactive protein has been studied for years and has been found to have a substantial effect on modern-day medicine. The C-reactive protein's structure is quite involved within the human body. However, its biological role of being able to protect against infections and to present a biological marker has allowed medical professionals to diagnose and treat patients better clinically. Most of the action that CRP partakes in, whether it be in a pro-inflammatory response or an anti-inflammatory response, is dependent on its own action. Functions regarding CRP are widely unknown still today, but with modern-day technology, the research regarding CRP is continuing to develop and will allow further advances in clinical decision making. This is a sample scene created with SAT to color by Group, and another to make a transparent representation of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.

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Adam Miller