Introduction To Macromolecules
Introduction to Cells at a Molecular Level
Overview: The Molecules of Life
All living things consist of four primary classes of large biological molecules:
Carbohydrates
Lipids
Proteins
Nucleic Acids
Molecular Structure Determines Function
The function of a molecule is inherently linked to its structure.
Small Organic Molecules
Small organic molecules can combine to form larger molecules known as Macromolecules.
Definition:
Macromolecules: Large molecules made up of lots of covalently connected atoms.
Representative structure of covalent bonding:
Hydrogen and Carbon atoms contributing electrons in covalent bonds.
Macromolecules as Polymers
Polymers: Macromolecules that are constructed from monomer building blocks.
Definition:
Polymer: A long molecule consisting of many similar building blocks (monomers).
Three classes of life’s organic molecules that are polymers:
Carbohydrates
Proteins
Nucleic Acids
The Synthesis of Polymers
Condensation Reaction/Dehydration Reaction:
Occurs when two monomers bond together, resulting in the loss of a water molecule.
Visualization:
During dehydration, a water molecule (H₂O) is removed to form a new bond.
Represented as:
Short polymer + Unlinked monomer → Longer polymer + H₂O
The Breakdown of Polymers
Hydrolysis:
A reaction that disassembles polymers into monomers by adding a water molecule.
Definition:
Hydrolysis is essentially the reverse reaction of dehydration.
Visualization:
Hydrolysis represented as:
Polymer + H₂O → Monomer + Bond broken
Reaction Rates
Both dehydration and hydrolysis reactions occur slowly without the assistance of enzymes.
Enzymes:
Macromolecules that catalyze and speed up these biochemical processes.
The Diversity of Polymers
Each cell contains thousands of distinct types of macromolecules.
Variation among macromolecules:
These macromolecules differ among cell types within an organism and have even greater variation among different species.
The immense variety of polymers arises from a limited set of monomers, enabling diverse biological functions.
Chirality
Chirality refers to the geometric property of a molecule that makes it non-superimposable on its mirror image.
Example molecular structures demonstrating chirality:
The arrangement of atoms and groups around a central carbon creates two possible configurations.
This is also deduced when molecular structures contain 4 different groups around a carbon
Chemical Groups and Their Properties
Overview of common chemical groups involved in biological molecules:
Hydroxyl Group (-OH)
Compound Name: Alcohol
Example: Ethanol (H-C-C-OH)
Carbonyl Group (>C=O)
Compound Names: Ketone, Aldehyde
Examples: Acetone (H-C-C(=O)-H)
Carboxyl Group (-COOH)
Compound Name: Carboxylic Acid or Organic Acid
Example: Acetic Acid (H-C(-COOH)-H)
Amino Group (-NH₂)
Compound Name: Amine
Example: Glycine (H-NH₂-C)
Sulfhydryl Group (-SH)
Compound Name: Thiol
Example: Cysteine (H-C-CH₂-SH)
Phosphate Group (-OPO₃²⁻)
Compound Name: Organic Phosphate
Example given structurally depicted.
Methyl Group (-CH₃)
Compound Name: Methylated Compound
Example: 5-Methylcytosine (N-CH₃)