All cells are surrounded by a plasma membrane, which controls the entry and exit of substances, exhibiting selective permeability.
Selective permeability differs from semi-permeability, which allows molecules smaller than the wall’s holes to pass while blocking larger molecules.
The basic structure of the plasma membrane is formed by amphipathic phospholipids:
Hydrophilic head (polar): Composed of a phosphate group attached to a glycerol molecule.
Hydrophobic tails (nonpolar): Made of saturated or unsaturated fatty acids.
Phospholipids arrange into a bilayer:
Polar heads face outwards toward aqueous environments.
Nonpolar tails face inward, away from water.
Integral proteins or transmembrane proteins span the plasma membrane. They can have structures such as alpha-helices or beta-sheets.
Their orientation in the membrane is dictated by their hydrophilic and hydrophobic regions.
Peripheral proteins are associated with the membrane surface, often as glycoproteins, aiding in cell recognition and attachment.
Proposed by Jonathan Singer and Garth Nicolson in 1972, the fluid mosaic model describes:
The plasma membrane as a mosaic of phospholipids and proteins, allowing flexibility and fluid movement across the bilayer.
Membranes are flexible, self-sealing, and capable of fusing with other membranes (e.g., vesicles with plasma membrane).
Archaea have ether linkages in phospholipids, making their membranes more chemically stable compared to bacteria and eukaryotes, which have ester linkages.
Archaeal membranes can also have branched lipid structures, in contrast to the unbranched structures found in Bacteria and Eukarya.
Bacterial cell walls are primarily made of peptidoglycan (murein), composed of alternating N-acetylglucosamine (NAG) and N-acetylmuramic acid (NAM), forming a rigid structure reinforced by tetrapeptide bridges.
Gram-negative bacteria: Have a thin layer of peptidoglycan and an outer membrane containing lipopolysaccharides, which can cause strong immune reactions.
Gram-positive bacteria: Possess thick peptidoglycan layers supplemented by teichoic acids, strengthening the wall and playing a role in ion movement.
The glycocalyx, a protective extra layer forming a sugar coat, is essential in biofilm formation and pathogenicity. It usually consists of polysaccharides and may appear as a capsule (organized) or slime layer (loose).
Bacteria in biofilms communicate and may exhibit different behaviors than free-floating counterparts.
Eukaryotic cells have well-defined nuclei and often contain organelles such as mitochondria (energy production) and chloroplasts (photosynthesis).
This complex system includes structures like the nuclear envelope, endoplasmic reticulum (smooth and rough), and the Golgi apparatus, facilitating intra-cellular transport and modification of proteins and lipids.
The cytoskeleton is composed of microfilaments, intermediate filaments, and microtubules:
Microfilaments: Involved in cell movement (e.g., muscle contraction, amoeboid motion).
Intermediate filaments: Provide structural support and anchor organelles.
Microtubules: Play roles in transportation within cells, cell shape, forming flagella and cilia, and chromosomal movements during mitosis.
Flagella and cilia have a characteristic 9+2 microtubule arrangement, allowing for locomotion or movement across the cell surface.
Understanding the cell membrane and its components is vital for comprehending how cells interact with their environment, transport substances, and maintain homeostasis. The structural differences between prokaryotic (particularly bacterial) and eukaryotic cells exemplify the diversity of life and the evolutionary adaptations that have occurred over time.