Infant diagnosed with circulatory problems & anemia; infants blood cells under microscopic examination look banana shaped; family has history of sickle cell

Upstream Causes

circulatory problems & anemia

Banana shaped red blood cells

Downstream causes:

Background Information

Sickle cell

4 types of macromolecules

Proteins

Enzymes

Transport

Nucleic acids

Carbohydrates

Lipids

Structural

Storage

DNA

RNA

Simple

Complex (many sugars)

Sterols

Fats

Phospholipids

Ex: Ferritin

Ex: Digestive enzymes (Amylase)

Ex: Hemoglobin

Ex: Keratin and collagen

DeoxyriboNucleic acid (Deoxyribose sugar)

Organ System functions:

Four types of amino acids:

Ribonucleic acid (Ribose sugar)

Found in nucleus

Found in cytoplasm

Disaccharides (two sugars)

starch, glycogen and fiber

Monosacchaarides (one sugar)

glucose, fructose and galactose

Maltose, sucrose and lactose

Triglycerides

Cholesterol

Vitamin D

Hormones

Bile

Consumed fat

Stored fat

Lipid bilayer

Cell membrane

Forms of DNA

Double helix

two long chains of amino acids wrapped around together

Chromosomes

When a cell prepares to divide the genetic information duplicates and packages into x-shape structure

Chromatid (each half of the x; identical to each other)

Centromere (what connects the halves)

Nucleotides in DNA

A(Adenine), T(Thymine), G(Guanine), & C(Cytosine)

Four kinds of amino acids

Non-polar

Non-polar covalent bond

Sharing equally

No charge

Hydrophobic

Polar

Polar covalent bond

Partial positive and negative charges (dipoles)

Unequally sharing

Hydrophilic

Acidic (negatively charged)

opposite attracts creating ionic bonds

Four levels of protein structure

Primary structure

Sequence of amino acids in a protein (Amine and acid group)

Peptide bonds

Formed by dehydration synthesis (water molecule is formed and bonds amino acids)

Secondary Structure

when amine and carboxylic acid groups from different amino acids attract to each other

Structure: a-helices & b-sheets

Tertiary structure

it occurs because of the interactions of the functional groups with each other.

Structure: 3D shape of all amino acid chains

Quaternary structure

shape of all amino acids chains interacting with each other

functional groups:

Polar

Non-polar

Positively charged

Negatively charged

Hemoglobin

protein found in red blood cells; contains iron to maintain red blood cell its shape

Hydrogen Bonds

Formed by dipoles (opposites attract)

Forming ionic bonds (opposites attract

Forming ionic bonds (opposites attract)

Polar Covalent bond; sharing unequally

Non-polar covalent bond; sharing equally (disulfide bond)

Hydrogen bonds

Organs

Liver

Heart

Kidneys

Gallbladder

Bones

Skeletal system

digestive system

Urinary system

Cardiovascular system

Digestive system

Eyes

Nervous system

Basic (positively charged)

Opposite attract creating ionic bonds

Polar

hydrophilic

Partially negative/partially positive

like to interact with water

creating dipoles

hydrogen bonds

Non-polar

no charge

forming non-polar covalent bonds

Polar covalent bonds

Hydrophobic

do not like to interact with water

Acidic (negative charged)

Hydrophilic

like to interact with water

attracted to positively charged

creating ionic bonds

Basic (positively charged)

Hydrophilic

likes to interact with water

attracted to negatively charged

creating ionic bonds

Organ functions:

Red blood cells (erythrocyte)

4 types of macromolecules functions:

Red blood cells function

Spleen

Lymphatic system

Proteins

storage

stores metal ions & amino acids

no nucleus

no rough endoplasmic reticulum

no mitochondria

concave shape

Protein in red blood cells:

Hemoglobin

Quaternary Structure

four polypeptide

2 alpha chains

2 beta chains

oxygen transporting protein of red blood cells

transport oxygen to body cells

delivers carbon dioxide to the lungs

Hemoglobin (protein in red blood cells)

transports the oxygen from lungs to body and to exchange it for carbon dioxide

then carries the carbon dioxide back to the lungs where it is exchanged for oxygen

Hemoglobin S

abnormal hemoglobin cells causing sickle cell

sickle cell is a genetic disease caused by one nucleotide mutation in DNA sequence

hemoglobin now has an exposed hydrophobic(don't like water) region

causing the hemoglobin to change shape of red blood cells causing it to no be able to functions

Enzymes

Transport

Structural

speed up biochemical reactions

moves molecules across membranes or from one place to another

Provides shape and support

Lymphatic system

Nervous system

Digestive system

Skeletal system

Urinary system

Cardiovascular system

eliminates waste

breaks down food

protects body from pathogens

detects & responds to stimuli

provides body's framework & protects organs

transports and circulates blood throughout the body

Spleen

helps fight certain kinds of bacteria

Eyes

Nourish the cornea, removes waste products from lens & maintains shape of the eye

Bones

Gallbladder

Kidneys

Heart

Liver

pumps blood throughout the body

filters blood

support the body, protect organs & allow movement

Stores & concentrates bile

maintain overall fluid balance, regulates & filters mineral from blood

Nucleic acids

Carbohydrates

Lipids

DNA

RNA

Sterols

Fats

Phospholipids

gives genetic instructions for the development and function of a cell

tRNA

Provides energy to the body

Complex

Simple

quickly digested and absorbed

takes time to be digested

intracellular lipid transport & metabolism

major storage form of energy

in cellular membranes to protect the cell from certain substances

mRNA (messenger RNA)

tRNA (translator RNA)

AUGAUC...

Nucleotides

A(adenine), G(guanine), C(cytosine) & U(uracil)

AUG=Met (amino acid)

mRNA

the translator between mRNA and amino acids

contains nucelotides complementary to DNA and sending them out the nucleus into ribosomes

when your red blood cells are not functioning properly from sickle cell

caused by sickle cell disease

caused by a mutation in the genes making an abnormal hemoglobin which then causes a change in shape of the red blood cells

Mutation in the DNA sequence causing the change of one nucleotide resulting in the hemoglobin to change the shape of red blood cells

Organs & organ system affected:

Spleen

Direct:

spleen can become enlarged and painful from high amounts of blood

Indirect:

spleen becomes permanently damaged leading to surgical removal cause high risk infections to occur

hereditary condition

Eyes

Direct:

Sickle cell retinopathy; sickle cells are blocking the blood vessels in the eye from receiving oxygen

Indirect:

can worsen & lead to proliferative sickle cell retinopathy; causes bleeding into the eye, detachment of the retina, & blindness

Bones

Direct:

Indirect:

due to the sickle shaped blood cells it can cause episodes of severe pain in the bones

leading bone damage from getting ulcers or severe infections

Gallbladder

Direct:

Indirect:

Gallstones

high levels of bilirubin (substance produced when red blood cells breakdown)

Kidneys

Direct:

Indirect:

the kidneys isn't getting enough oxygen affecting it's overall function such as filtering or regulating

renal failure; needing blood transfusion or a transplant

Heart

Direct

Indirect:

Liver

Indirect:

Direct:

causing it to regrow in an unusual way affecting its function (structure dictates function)

blood transfusion can cause liver damage

hear tries to compensate; the four cardiac chambers dilate

heart failure; strokes

Lymphatic system

Cardiovascular system

Nervous system

Skeletal system

Digestive system

Urinary system

protein in the urine, urine with too much water or blood in the urine