SLP 1
Page 1: Introduction
Institution: Universiti Kebangsaan Malaysia
Document: Self-Learning Package on Cellular Biomolecules (CB-SLP-1)
Edition: Volume/Edition 2019
Target Audience: Medical Doctor (MD) Programme Students
Facilitator: Dr. Norwahidah Abdul Karim
Page 2: Learning Objectives
At the end of this topic, students should be able to:
Differentiate between prokaryotes and eukaryotes.
Describe the function of organelles and their inclusions.
Relate diseases associated with dysfunctions of these organelles.
References:
Lieberman, M. & Marks, A. (2018). Basic Medical Biochemistry: A Clinical Approach. 5th Edition. Lippincott Williams & Wilkins.
Baynes, J. & Dominiczak, M.H. (2018). Medical Biochemistry, 5th Edition. Elsevier Health Sciences.
Murray, R.K. et al. (2018). Harper's Illustrated Biochemistry 31st Edition. Appleton & Lange.
Ferrier, D.R. (2017). Lippincott's Illustrated Reviews. Biochemistry. 7th Edition. Lippincott Williams & Wilkins.
Nussbaum, R.L. et al. (2015). Genetics in Medicine. 8th Edition. Elsevier Health Sciences.
Online Resources:
http://journals.sfu.ca/paao/index.php/journal/article/viewFile/352/pdf
https://ghr.nlm.nih.gov/
Cellular Types:
Prokaryotic (e.g. bacteria) – no nucleus.
Eukaryotic (e.g. human cells) – contains a membrane-bound nucleus.
Page 3: Structure of Prokaryotic and Eukaryotic Cells
Prokaryotic Cell Structure:
Capsule, cell wall, plasma membrane.
Cytoplasm containing ribosomes, plasmids, and nucleoid (circular DNA).
Eukaryotic Cell Structure:
Cytoplasm enclosed by a plasma membrane.
Contains organelles such as centrioles, lysosomes, mitochondria, vacuoles, endoplasmic reticulum, nuclear envelope, and Golgi complex.
Page 4: Cell Membrane Overview
Cell/Plasma Membrane:
Encloses all human cells.
Composed of approximately 60% protein and 40% lipid.
Main lipid component: Phospholipid forming a bilayer due to hydrophilic and hydrophobic ends.
Functions:
Supports and retains cytoplasm.
Acts as a selective barrier for transport of nutrients and waste.
Allows selective transport of molecules; transport proteins often require energy.
Participates in cell communication and recognition.
Page 5: Organelles and Their Functions
Endoplasmic Reticulum (ER):
Two forms: Rough (with ribosomes) and Smooth (without ribosomes).
Functions: Mechanical support, synthesis of proteins and lipids, detoxification.
Golgi Complex:
Functions as a cellular post office: modifies, sorts, and packages proteins.
Lysosomes:
Contain digestive enzymes for cell maintenance and destroying damaged cells.
Peroxisomes:
Contain enzymes to break down peroxides; deficiencies lead to diseases like adrenoleukodystrophy.
Page 6: Mitochondrial Structure and Function
Mitochondria:
Have a double membrane: outer membrane and highly folded inner membrane (cristae).
Main function: ATP production (energy currency of the cell).
Contain their own DNA and ribosomes; possibly originated from ancient prokaryotic cells.
Ribosomes:
Composed of rRNA and protein; found in cytoplasm or on rough ER.
Main function: protein synthesis.
Page 7: Comparison Between Cell Types
Differences between Prokaryotes and Eukaryotes:
Key features such as nucleus presence, number of chromosomes, organelles, and cell structures.
Examples of Cellular Components:
Key structures defining prokaryotes and eukaryotes such as lysosomes, mitochondria, Golgi apparatus, etc.
Page 8: Protein Synthesis Processes
Ribosomes and Rough ER:
Ribosomes synthesize proteins; rough ER aids in their folding and modification.
Golgi apparatus modifies, sorts, and packages proteins for their cellular destinations.
Protein Pathways:
Various vesicle pathways exist, directing proteins to the membrane or lysosomes.
Page 9: Mitochondrial Function and Disease Association
Structure Suitable for ATP Production:
Discuss the adaptations of the mitochondrial structure that facilitate efficient ATP synthesis.
Diseases Linked to Organelles:
Various organelles such as mitochondria or peroxisomes related to specific diseases:
Zellweger syndrome
Leber's hereditary optic neuropathy
Von Gierke's disease
Tay-Sachs disease
I-cell disease.
Each listed condition can be further explored for its link to organelle dysfunction.