Monday, January 6, 2014

The Heart

The human heart has four chambers and they are the right atrium, left atrium, right ventricle and left ventricle. The septum is a muscular wall that separates the right side of the heart from the left. The right side of the heart pumps deO2 blood to the lungs and the right side of the heart pumps O2 blood to the body systems. The atria are the receiving chambers, the right atrium receives deO2 blood from body systems via the superior and inferior vena cava, the left atrium receives O2 blood from the lungs via the pulmonary veins. The ventricles are sending chambers. The right ventricle sends deO2 blood to the lungs through the pulmonary valve, pulmonary trunk and the pulmonary arteries. The left ventricle sends O2 blood to the body systems through the aortic valve and aortic arch or dorsal aorta.


The heart has other things that make it works, for example, Atrioventricular valves separate the atria from the ventricle. There are two different types of AV valves and they are tricuspid valve which is on the right side and the bicuspid valve which is on the left side. They open when the atria contract and close when the ventricle contracts to prevent backflow. The chordae tendinae are tendon-like pieces of tissue, they keep the AV valves from inverting when the ventricles contract. Papillary muscle holds and supports the chordae tendinae.

The SA node if found along the wall of the upper right atrium chamber, it stimulates the simultaneous contraction of the atria and sends a nerve impulse to the AV node. The SA node initiates the heartbeat, this is why it has a nickname of being the pacemaker. The  AV node is in the lower right atrium close to the AV valve. When the AV node receives the nerve impulse from the SA node it fires to initiate the contraction of the large ventricles by sending the message through the purkinje fibres. All of this is what moves our blood around our body and it is what we feel when we feel the pulse or listen to the heartbeat.

EKG (Electrocardiogram)
This is a machine the measures the systolic and diastolic of the heart. It is measured and is represented by the letter P,Q,R,S and T. The P represents the simultaneous contraction of the atria (caused by the SA node), the QRS is the contraction of the ventricles (caused by the AV node and purkinje fibres) and the T is the recovery of the ventricles.
P= atrial systole (contract)
R= ventricular systole (contract)
S= atrial diastole (rest)
T= ventricular diastole (rest)
 
HOW DOES THE HEART BEAT ON ITS OWN?
The regulation of the heartbeat is under the influence of the autonomic nerve system. The part of the brain that governs the speed of the heart rate is called the medulla oblongata. It will speed up or down the heart rate when needed. Under normal circumstances, the heart controls itself. This is why the heart can still beat 2-5 min after it is removed from the body.
 
BLOOD PRESSURE
High blood pressure (hypertension) puts a constant strain on the tissues and it may cause capillaries to burst. If this happens in the brains it is a stroke, if it happens in the heart then it is a heart attack. The longer a person has high blood pressure, the greater the potential for tissue damage. Sometimes high blood pressure is normal for example when doing physical activities, but the brain should return the blood pressure back to normal (lower level). Low blood pressure (hypotension) is particularly not a good thing to have either. It can result from genetics, anemia, dehydration, blood loss and shock. Proper kidney function can only be maintained if there is a sufficient pressure for filtration. Some factors that can affect blood pressure can include:
1. Vessel Diameter (bigger=lower BP, higher=higher BP)
2. Blood viscosity (thick= higher BP, thin = lower BP)
3. Total Blood Vessel Length (more fat = higher BP, thinner = lower BP)
4. Cardiac output (faster heartbeat = higher BP, slower heartbeat = lower BP)
5. Stress (lots = higher BP, less = lower BP)

Circulatory system

In the Circulatory system there are five types of blood vessels and they are:
1. Arteries: Transport blood away from the heart. They have thick elastic walls so that the walls can expand when it needs too. The expansion of the arteries is the pulse we feel. Arteries are usually found deep and along bones in the body. This protects them from injury and temperature loss. Arteries have a very high blood pressure.

2. Arterioles: Control the blood flow to capillaries. They are smaller in diameter than arteries, they have thinner walls. They also have a pre-capillary sphincter, they contract and dilate to increases or decrease blood flow to a particular capillary bed. Arterioles are located leading towards all capillaries. Blood pressure > osmotic pressure.
 
3. Capillaries: Connect arteries to veins and are the site of the capillary fluid exchange. They have very thin walls and are found everywhere within a few cells of each other.
 
4. Venules: They drain blood from the capillaries and join to form veins. They have thinner walls then veins. The are located often near the surface. Osmotic pressure > Blood pressure.
 
5. Veins : Transport blood towards the heart. Veins have inelastic walls that contains valves that prevent blood from flowing backwards.They are often near the surface and are surrounded by skeletal muscle. 'squeeze' the blood along. Blood pressure and velocity is much lower than in arteries.

 
 
Some major arteries and veins are:
1. Subclavian arteries bring blood to the chest wall and arms. Subclavian veins bring blood away from the chest wall and arms to the superior vena cava of the heart.
2.Carotid arteries bring blood to the brain. Jugular veins carry blood away from the brain to the superior vena cava of the heart. 
3. Mesenteric arteries bring blood to the digestive system. Then the hepatic portal vein carries the blood from the digestive system to the liver. The Hepatic vein takes the blood from the liver to the inferior vena cava of the heart. The Hepatic arteries tale blood from the heart to the liver.
4. Renal arteries take O2 blood to the kidneys and the renal veins takes the deO2 blood from the kidneys to the inferior vena cava of the heart.
5. Iliac arteries take O2 blood from the heart to the trunk and legs and the iliac veins takes the deO2 blood from the trunk and legs to the inferior vena cava of the heart.
6. The coronary Arteries brings O2 blood to the heart and the coronary vein takes deO2 blood from the heart to the inferior vena cava.
7. The Pulmonary arteries take deO2 blood away from the heart to the lungs to get replenished with O2. The Pulmonary veins take O2 rich blood from the lungs into the heart where that blood will be sent out to the rest of the body systems.
 
The aorta take O2 blood to the arteries for the top part of the body the dorsal aorta takes O2 blood to the arteries involving the lower part of the body.
Systemic circulation is the system of blood vessels that delivers O2 blood to the body systems. Pulmonary circulation is the system of blood vessels that delivers deO2 blood to the lungs to be replenished with oxygen.
 

How to do a blood trace: To do a blood trace you follow the way the blood goes through the body and name all the parts it goes though. For example:
  Something that can help you do this if you don't have the circulatory system memorized is this: 
However, it is better that one memorizes the system.

 Fetal Circulation
 
A fetus does not use its lungs, it receives O2 blood from the placenta. There are four features that fetus' have that adults do not and they are:
Foramen Ovale: This is an opening between the left and right atria, it is covered by a flap that acts as a valve. It allows the blood to by pass the lungs and reroutes most of the blood from the right atrium into the left atrium.
 
Ductus Arteriosus (Arterial Duct): This is a small arterial connection, like a shunt, between the pulmonary artery and the aorta. It further allows blood to bypass the lungs.
 
Umbilical Cord: Has three blood vessels traveling through it. The largest one is the umbilical vein, which transports blood with oxygen and nutrients to the fetus. The other two are the umbilical arteries, which branch off of the iliac arteries in the fetus and take used (CO2 and wastes) blood back into the mother via the placenta.
 
Ductus Venosus: This blood vessel connects the umbilical vein to the vena cava. The O2 blood from the umbilical vein mixes with deO2 blood in the vena cava. The duct venosus bypasses the liver and this blood is sent directly to the heart, blood will eventually go to the liver but not until it reached the hepatic portal vein. This is why the fetus is so susceptible to toxins in the blood.
 
 
 
Lymphatic System
The lymphatic system has four main jobs and they are to take up excessive tissue fluids, transport fatty acids and glycerol, fight infections and to trap and remove cellular debris. This system consists of Lymph ducts and capillaries that drain and collect excess fluids from tissue and takes the fluid to nodes to be cleaned. The cleansed lymph then travels through lymph duct to the Subclavian vein where they are dumped into the inferior vena cava. Lymph nodes remove debris from lymph. It contains phagocytic lymphocytes. WBC make antibodies and attack invaders. Lactaels absorb and transport fatty acids and glycerol in the villi of the small intestine. Other organs in the lymphatic system are tonsils, appendix, spleen and thymus gland.
 
Blood
Blood is made up of  three things: 55% of Plasma, less than 1% of White blood cells(Leukocytes) and platelets(Thrombocyte), and 45% or red blood cells (Erythrocytes). The Plasma potion of the blood is 91% water which maintains blood volume and transports molecules. 7% is proteins which are clotting proteins, albumin and immunoglobulin (antibodies). 2% is miscellaneous things that must be carried around the body, for example, salts, gases, nutrients, wastes, hormones , vitamins and hormones.
 
Red Blood cells (Erythrocytes): They have not nuclei and transports CO2, O2 and H+ ( acts as a buffer). They look like doughnuts without the hole all the way through it and are dark purple to bright red. Typically, they live for about four months. Erythrocytes contain hemoglobin molecules, carbonic anhydrase and antigens. They are made in the red bone marrow.
 
White Blood Cells (Leukocytes): They make histamines, antibodies and hunter killer cells. Their purpose is to fight infections. They can squeeze out of blood vessels to attack invaders. To distinguish a leukocyte it has a strangely shaped nuclei. They are also made in the red bone marrow.
 
Platelets (Thrombocytes): These are just fragments of cells with no nuclei. They are mad in bone marrow and we make about 200 billion a day. Thrombocytes are used to aid in blood clotting and can recognize micro tears in blood vessels and bind together to form a blood clot.
 
Antigens, Antibodies and Blood Type
 
An antigen is and identification protein on a RBC. It is a glycoprotein on the RBC membrane. There are two types of antigens on human RBC: A and/or B. A person can have one of the four different types of blood: Antigen A--> type A blood, Antigen B---> type Blood, Antigen A and B ----> type AB blood or No Antigen ---> type O blood.
An antibody is a protein designed to combat any foreign protein. They are made by WBC and will bind to foreign protein with foreign antigens, this will cause agglutination (clumping). WBC's will then destroy the agglutinated cells. Our blood has antibodies that are opposite the antigens we have on our RBC's, so we do not attack our own blood.  


Capillary Fluid Exchange
Net blood pressure forces water out of the blood into the interstitial fluid. The water carries O2 and nutrients with is out. Because there is more O2 and nutrients in interstitial fluid, it diffuses into body cells. The large things for example RBC, WBC, platelets and blood proteins stay in the capillary because they are too big to leave. Since most of the water has left, the blood becomes very concentrated. The venule side of the capillary is therefore under great osmotic pressure to draw back water into the blood. The water carries CO2 and metabolic wastes(urea), these are carried to the kidneys and other excretory organs to be removed.

Sunday, January 5, 2014

Digestion system

The digestive system includes many different parts that are needed to be able to actually digest food. This is what they are and what they do:
1. Mouth: This is where the digestion process starts off at. Mechanical digestion and chemical digestion. The difference between them is that mechanical digestion is where the food is actually physically being torn apart. And chemical digestion breaks down the food by using enzymes.
2.Teeth: take in the food and start to mechanically digesting it by breaking food into smaller pieces.
3. Tongue: Contains taste buds. They tastes sweet/salty at the top of the tongue, sour on the sides of the tongue and bitter at the back. Tasting bitterness can save our lives because poisons most often taste bitter. The tongue also moves the food around the mouth and towards the teeth to mix the food and the saliva.
The final job of the tongue is that it pushes the bolus of the food to the back of the throat to the 'swallow reflex center'.
4. Salivary Glands: are ducted glands that produce saliva. The saliva liquefied food, contains amylase and begins to chemical digest, lubricates and softens the bolus of food and it also has an enzyme (lyric enzyme) in saliva kill bacteria.
5. Pharynx: is located at the back of the throat, which opens to both the respiratory and digestive systems. When food is places on the 'reflex center' by the tongue three things happens. The soft palate covers the opening to the noes, the epiglottis covers the trachea and peristalsis of the esophagus begins. 
6. Epiglottis: is a flap that covers the trachea tube so that food does not go down the trachea.
7. Esophagus: is a 30 cm long tube that connect the pharynx to the stomach. No digestion occurs here. Food moves through the esophagus (and the rest of the digestive tract) by a process called peristalsis, which is a slow, rhythmic contraction that pushes the bolus along.
8. Cardiac Sphincter: is a ring of muscle located at the beginning of the stomach which stops food from re-entering the esophagus. 
9. Stomach: is a J shaped organ that can hold 23 liters of food. It also contains the circular and longitudinal smooth muscle layers, but also has a third muscle layer in the transfers. It churns food and liquefied it which is mechanical digestion. This process is helped by the ridges in the mucosa layer of the stomach. It has gastric juices which are pepsinogen (inactive), hydrochloride acid (acid) and mucus (protects). HCl is release when protein enter the stomach, it transforms pepsinogen into and active hydrolytic enzyme pepsin. Pepsin then digests proteins into smaller polypeptides.
10. Pyloric Sphincter: is located at the base of the stomach and it will meter out the chyme into the duodenum at a slow, constant rate. 
11. Duodenum: is the beginning of the small intestine. The walls of the duodenum release intestinal juices (pancreatic juices are released before) which are peptidases, nucleases, maltase, lactase and sucrase. Peptidases breaks di/tri peptides into amino acids. Nucleases breaks nucleic acid into nucleotides. Maltase digests maltose into glucose and glucose. Lactase digests lactose into glucose and galactose. Sucrase digests sucrose into glucose and fructose.
12. Liver: Has over 500 functions. It destroys old red blood cells ( convert hemoglobin to bile), produce bile, detoxifies blood, deamination of amino acids (gluconeogenesis)(birth of sugar), makes blood clotting proteins, makes urea and regulates the blood glucose level at ~0.1% of plasma. 
13. Gall Bladder: Stores bile that the liver made. When the gall bladder receives a message from the hormone CCK, it releases bile into the common bile duct, which dumps into the duodenum. The purpose of the bile is it emulsifies fats in the duodenum.
14. Pancreas: is both an endocrine gland and a exocrine gland. This means that it produces hormones and digestive juices. The hormones the pancreas makes are insulin and glucagon. These hormones are made in the specialized cells of the pancreas called 'the islets of Langerhans'. Insulin is used when there is more than 0.1% glucose in the blood, the pancreas releases the insulin and it will cause the liver to convert the glucose to glycogen for storage, it promotes the formation of fats and causes the protein in cell membranes to open and allow the entrance of glucose into cells. This results in lower blood sugar levels. Glucagon is used when there is less than 0.1% glucose in the blood, the pancreas releases the hormone glucagon and it will cause the liver to convert glycogen into glucose to be released into the blood. This will result in higher blood sugar levels. The pancreatic juices that the pancreas releases are sodium bicarbonate, pancreatic amylase, lipase, trypsin and nucleases. Sodium Bicarbonate is released to neutralize the stomach acid(pH of 2.5) to a pH of 8.5. Amylase converts uncooked starch to maltose. Lipase converts lipids to fatty acids and glycerol. Trypsin converts small polypeptides into di/tri peptides. Nucleases converts nucleic acids into nucleotides. The pancreatic juices are released into the duodenum where they are then used to break down the chyme.
15. Small intestine: has three parts: duodenum(starts chemical digestion), jejunum(finishes digestion and begins absorption) and the ileum(absorbs all of the nutrients into the circulatory and lymphatic systems). The small intestine has an increased rate of absorption due to its highly convoluted walls with very large surface area. There are fold in the mucosa layer called villi which increase the surface area for absorption. The villi also has smaller folds called micro villi. The absorption of nutrients takes place through the columnar cells of the micro villi which involves active transport and requires a lot of energy. Sugar and amino acids are absorbed by the mesenteric capillaries (blood stream) and glycerol and fatty acids are absorbed by the lacteal ( lymphatic system).
16. Appendixsits at the junction of the small intestine and large intestine. It’s a thin tube about four inches long. The function of the appendix is not known.

17. Large Intestine(colon): it is larger in diameter but is much shorter in length than the small intestine. It has 4 main parts which are the ascending colon, transverse colon, descending colon and sigmoid colon(rectum). The large intestine absorbs water and salts that were used in the digestive process. It also has E.Coli bacteria that live in it. The E.Coli has four things that they do which are, slow the movement through the colon which allows time for water to be reabsorbed, they eat the wastes and produce useful things that we new to survive like vitamin K and amino acids, they also produce growth factor and the produce waste of there own (methane gas). By the end of the large intestines the waste are transformed into feces. If the waste move through the intestine too quickly it cannot absorb enough water resulting in diarrhea, if it goes to slow it will absorbed too much water resulting in constipation.
18. Rectum: Is the terminal portion of the large intestine, extending from the sigmoid colon to the anal canal. It acts as a temporary storage site for feces.
19. Anus: is the last part of the digestive tract. The anus is where the feces leaves the body. 


The 3 Hormones that control digestion!

Gastrin: when food is present in the stomach gastrin is released and this causes the cells of the stomach mucosa to release gastric juices.
Secretin: is released when there is acidic chyme in the duodenum, this hormone causes the pancreatic juices to be released. 
Cholecystokinin (CCK): is released when fats and proteins enter the duodenum, it is released into the blood stream and I causes the gall bladder to secrete bile and the pancreas to release it's pancreatic juices with digestive enzymes. These juices are sent to the duodenum where the enzymes can begin the digestion of lipids and proteins.


And that is everything I know about the digestive system!

Sunday, November 17, 2013

Protein Synthesis

 
Protein Synthesis video^
 
    Protein Synthesis has two main steps and they are transcription and translation. Transcription is where it makes a copy of one gene in DNA into mRNA. Translation takes the mRNA and translates it into a protein. We will take a closer look into these steps.
  TRANSRIPTION: 1. The enzyme helicase unwinds and unzips one gene of the DNA. 2. Complementary RNA base pairing attaches to form a mRNA 3. The enzyme RNA polymerase forms a sugar phosphate backbone and checks for mistakes. 4. The mRNA detaches and leaves the nucleus through the nuclear pores and the DNA winds back up.
TRANSLATION: 5. mRNA moves to join a ribosome in the cytoplasm 6. Initiation (the first codon on any mRNA molecule is called the initiator) 7. Elongation: ribosomes job is to position the tRNA with its corresponding amino acid onto the matching mRNA molecule. Then the amino acids bond together with a peptide bond and with the help of the enzyme peptidyl transferase. 8. Termination: the last codon on any mRNA chain. The last codon is the stop codon and it does not have a matching amino acid so that is the message to stop. The amino acid chain then detaches and is considered a protein.

 
      Below is the way that the sequence of DNA is transformed to mRNA and then to tRNA and then to amino acids. From DNA to mRNA they just pair up with their complementary base pairing and since it is turning into an RNA strand there is no Thymine, in its replace there is Uracil. From the mRNA to tRNA they do the came thing find their complementary base pairs. A short cut to this is just to look back at the DNA strand and change all the Thymine's to Uracil's. To find the matching amino acids to the tRNA you look at the mRNA strand and find them on the mRNA codon chart.
 
 
 MUTAGENS
    Some environmental mutagens are UV rays, gamma rays, ionizing radiation, caffeine, aflatoxin (from mold) and ISD. There are two types of mutations that can come from these mutations they are gene mutation or chromosome mutation. A gene mutation is the change of one or more nucleotides in a single gene. This affects the outcome of the protein and might affect the job that the protein does. A chromosome mutation is a mutation of all or part of a chromosome, which affect many genes. A chunk of the chromosome may be missing/or added. This affect many genes which will also affect the proteins being made. When a protein is made it is made to do a specific job, so when the protein gets messed up the job also gets messed up causing abnormalities. For example, extra limbs, downs syndrome or even making a person have male and female parts.

    A genetic disorder is an illness caused by one or more abnormalities in the genome, especially a condition that is present from birth. Two examples of these are Klinefelter syndrome and Turners Syndrome. Klinefelter syndrome is when there is an extra sex chromosome. For example, a persons sex chromosomes are XXY instead of XX or XY. This causes the person to have both female parts and male parts (breasts and testies). If one has this syndrome their IQ is usually impaired.  In the Turners syndrome the person is missing a sex chromosome. So their sex chromosome is usually just X. This causes women to be short and have a fold in the neck when they are young and they cannot have babies. Also, their breasts don't develop properly.

Biological molecules

DEHYDRATION SYNTHESIS AND HYDROLISIS
   Dehydration synthesis joins monomers together by taking H2O away, hence the dehydration part of the name. On the other hand, hydrolysis is the exact opposite of dehydration synthesis it is the breaking of polymers into units by adding H2O. Here is a link to a video that shows you a better understanding of these two concepts: http://youtu.be/_Ai5NyQ_ttE

This is dehydration synthesis. See how it is taking away the H2O and then the two monomers bond together with the oxygen and become a polymer.


     This is hydrolysis. See how they are ADDING H2O which causes the polymers to split apart and become monomers.




CARBOHYDRATES
The name comes from hydrated carbons. Carbohydrates empirical formula is (CH2O)n where n equals the number of times the chain is repeated. Carbs are made up of C,H and O and have a ratio of 1carbon:2hydrogen:1oxygen. 
There are a couple different types of carbohydrates. The first type is monomers which are monosaccharaides. Specific examples are glucose, fructose, ribose and deoxyribose. Another type of carbohydrates are disaccharides, this is when 2 monosaccharaides join together. Some examples are; glucose+glucose forms maltose, glucose+fructose form sucrose and galactose+glucose form lactose. The last type is polysaccharides. This is when many saccharides are joined together forming what looks like a chain. There are 4 different types of polysaccharides that i will go deeper on and explain them a bit more, which are cellulose, starch, glycogen and chitin. 
     Cellulose is a long chain without any side chains. One can remember this by thinking of celery and how celery is straight just like the chain of glucose molecules. Plants use cellulose as protection and structure, it is in the cell walls of plants. The linkage between the carbon atoms of sugars are different than the bonds in starch and glycogen, no mammal can break this bond. This is why we cannot digest cellulose(fiber). 


     Starch is made up of many glucose molecules linked together in a straight chain with a few side chains. Plants store their energy as starch. Below is a picture of a starch chain, notice how it only has one side chain.

  Glycogen is made up of many glucose molecules linked together with many side chains, unlike starch that only has a few. Glycogen is very important to us animals. We store our energy as glycogen in our liver and muscles.  Below is a picture of a glycogen chain. Again notice how it has more than just one side chain. If this picture was extended then you would be able to see how it has many side chains as suppose to starch. 

  
  The last polysaccharide is chitin. It is made by animal and fungi. Chitin is made of long glucose chains linked with covalent bonds, which are very strong. It makes structures like exo-skeleton, fingernails, claws and beaks. This is was chitin looks like structurally.

A main function if carbohydrates is energy. When the bonds between carbon atoms are broken, the energy is released and can be used by cells. Starch stores energy in plants, and glycogen stores energy in animals. Another function is structural. Cellulose is the major structural and protection compound in plants.
 
 
 
LIPIDS
     There are 4 main uses for lipids and they are long term storage for energy, insulation and protection, they make some hormones(ie. steroids) and they are the structure of the cell membrane. The structure of a lipid is made up of Carbon, Hydrogen and Oxygen, just like a carbohydrate. However, in a lipid there is no set ratio for these elements. There are three types of lipids and they are triglycerides(neutral fats), phospholipids and steroids.
     Triglycerides are composed of three fatty acids bonded to one glycerol. The fatty acids contain a long chain of carbons with an acid end. The glycerol is a small three carbon chain with three alcohol(OH) groups. The fatty acid and glycerol bond together via dehydration synthesis. There are two types of triglycerides which are saturated and unsaturated fats. The difference between these two types of triglycerides are that in a saturated fat there is no double bonds in the carbon chains of the fatty acids, where in a unsaturated fat there is one or more double bonds. Also, a saturated fat is solid at room temperature, come from animals and are considered unhealthy. A unsaturated fat is liquid at room temperature, come mostly from plants and are considered healthy.

 
     Phospholipids are used to make up the two layered cell membrane of all cells. They are similar to a triglyceride but the third fatty acid group of a triglyceride is replaced by an inorganic phosphate group (PO4 3-). A phospholipid has a polar head that is water soluble(hydrophilic) and the non-polar tail is not water soluble (hydrophobic). There are a couple different ways that they display phospholipids. Here are some of them:



 
 
 
   A steroid is the last type of lipid I will be talking about. Steroids look different than all the rest of the lipids. They are made up of four carbon ring and the molecules are fused together. They kind of look like four honeycombs stuck together. The use of steroids is to create some hormones, cholesterol and vitamin D. Some types of steroids are testosterone, estrogen, cholesterol and vitamin D.
 
 
PROTEIN
     The functions of a protein is structural because they help make up all structures in living things for example, actin and myosin are muscle proteins, keratin is found in like nails and hair, collagen is found in bones, teeth, cartilage etc. Another function of a protein is functional, they help our bodies functioning properly and to digest our food. This is done by enzymes, which are proteins that are catalysts which speed up reactions and control all cell activities. The final function of a protein is they can act as a food source, once we have used up all of our carbohydrates and fats, proteins will be used for energy. However, proteins are worth the least amount of energy that is why they are saved for the last resort.  Proteins are made up of carbon, hydrogen, oxygen, nitrogen and maybe sulfur but in no set ratio. Proteins are chains of amino acids that bond together via dehydration synthesis. An amino acid has three parts: Amine Group (NH2 or HH3+) which acts as a base(accepts H+), Carboxyl Group (COOH or COO-) and it acts as an acid (donates H+) and the R Group which have twenty different combinations. When amino acids bod together they bond with a peptide bond which is formed between carbon and hydrogen and one water molecule is lost. If only two amino acids are together it is called a dipeptide if the chain becomes three then it is called a tripeptide. After that, when the protein chain has more than three amino acids it is called a polypeptide. Every protein is different because the order of amino acids are different.
 
 
   The levels of Protein Structure:
       Primary structure is simply when the amino acids bond together with peptide bonds. The protein depends on the order of the amino acids, if they are not in the right order then the protein may not be able to do its job.
       Secondary structure is when hydrogen bonds form between the amino acids positive (amine group, NH3+) from one amino acid and negative(carboxyl group) from a different amino acid. This bond makes the chain twist into either an alpha helix or a beta pleated sheet.
       Tertiary structure happens between the R Groups. The interactions is between  + and - attractions and sulfur sulfur bridges. The positives and negatives will attract each other and the same charges will repel each other. That makes the structure to fold into a highly specific 3-dimentional shape. The shape determines the protein's job or role it will play in the body.
      Quaternary structure is not seen in all proteins, this is where two or more molecules join together with an ionic bond to form a functional protein. Some examples are Insulin with two subunits or Hemoglobin with four subunits.
 
 
NUCLEIC ACIDS
 
   Nucleic acids are acidic molecules that are found in the nucleus of cells. There are two type and they are deoxyribonucleic acid(DNA) and ribonucleic acid (RNA). All nucleic acids are made up of units called nucleotides which are made up of three sub-molecules: Pentose sugar(ribose or deoxyribose), Phosphate, Nitrogen base (purine or pyrimidine). Adenine and Guanine are purines, they have two rings and are both found in DNA and RNA. Cytosine, Thymine and Uracil are pyrimidine's, they have only one ring and Cytosine is found in both RNA and DNA, however, Thymine is found in DNA and Uracil is found in RNA. A purine always matches up with a pyrimidine in a nucleic acid. A memory trick for a purine is "Its got 2 be GAp". The 2 represents the two rings and the GA represent Guanine and Adenine. A memory trick for pyrimidine is that "CUT the pyramid". The CUT stands for Cytosine, Uracil and Thymine and the pyramid reminds one of the single blocks the Egyptians had to cut for the pyramids, therefore it has one ring.
 
  A DNA strand is composed of nucleotides and a sugar phosphate backbone. The nucleotides go together with their complementary base pair, which is A-T and G-C. Adenine and Thymine bond together with two hydrogen bonds and Cytosine and Guanine bond together with three hydrogen bonds. The sugar phosphate backbone is formed after all of the complementary bases are paired up then it twist into a double helix. The main function a DNA is to direct and control all cell activities by making proteins and enzymes. The also contain all of the genetic information necessary to make one complete organism.
 
   Some of the difference between RNA and DNA is that DNA is confined to the nucleus and RNA can move to the cytoplasm. RNA has ribose sugar instead of deoxyribose and RNA has Uracil instead of Thymine like DNA. DNA is a double helix as suppose to RNA is a single helix. There are three types of RNA (mRNA, tRNA, and rRNA) and there is only one type of DNA. RNA's function is mainly to assist DNA in making proteins.
 
    Adenosine Triphosphate:
ATP is also thought of as a nucleic acid because it has a similar structure as a nucleotide. The only difference is that it has three phosphate groups instead of one. In a ATP molecule there is three phosphates (Triphosphate) a sugar and an adenine (Adenosine). ATP is the energy source of the body. This is because it takes a lot of energy to put two phosphate molecules together so when they are broken apart a lot of energy is released.