Mitochondria
are the cells' power sources. They are distinct organelles with two membranes. Usually
they are rod-shaped, however they can be round. The outer membrane limits the organelle.
The inner membrane is thrown into folds or shelves that project inward. These are called
"cristae mitochondriales". This electron micrograph taken from Fawcett, A
Textbook of Histology, Chapman and Hall, 12th edition, 1994, shows the organization of
the two membranes.
Use
the study guide below to navigate through this unit. The links lead to
answers to the questions, in case you can't remember. If you can answer these questions, you will do
well on the exam.
Read pp 387-402 in Cooper
Use the excellent diagrams to
show how the different mitochondrial systems are interrelated and also how
proteins enter mitochondria. Study
the section on mitochondrial diseases and understand how they are
inherited. Finally, correlate
your learning from pp 398-402 with the biochemical lectures during the
previous week to fully understand the chemiosmotic theory.
Objectives of the unit on mitochondria.
-
Describe the basic
substructure of
mitochondria. Be able to correlate a change in structure with a change
in function.
-
Locate
each of the major sets of enzymes/functional groups: Kreb’s Cycle,
Electron transport chain, ATP synthetase, hydrogen pumps and describe
their significance.
- Be
able to specify exactly where and on what structures ATP is
synthesized.
- Define
the Chemiosmotic theory.
- Explain
the significance of an abnormal increase in number of mitochondria
and/or cristae in cells that have defective mitochondrial proteins.
-
Describe
how mitochondria replicate.
- Define
the function of mitochondrial DNA, RNA, ribosomes. Categorize the
proteins produced.
- Distinguish
mitochondrial inheritance from Mendelian inheritance.
- Describe
general functions for TOM and TIM proteins in mitochondria.
- List
the major steps involved in protein entry into mitochondria
(preparation, binding, guiding, entry, final steps in matrix).
- Describe
how products of mitochondria may leave
for the cytoplasm.
- Describe
how the electron transport chain facilitates the following:
-
ATP
synthesis
-
ATP/ADP
transporter
-
Entry
of proteins
- Define
the steps used by the cell to destroy old mitochondria
- Describe
how mitochondria are involved in
steroid hormone production.
- How
are mitochondria involved in apoptosis?
Competencies
Given
the origin of a specific mitochondrial protein, be able to trace its route
into mitochondria and be able to predict the general outcome of a genetic
defect in the protein.
Describe
multiple examples where mitochondria functions are integrated and thus
facilitate one another.
Be
able to explain mitochondrial heredity to a patient and, if there is a
defect, why there is variability in severity of the disease in a given
family.
Test yourself!! How much do you already know about mitochondria?
Sample questions:
1)
Your patient has a genetic defect in a mitochondrial Kreb’s cycle
protein encoded by nuclear DNA. The
defect is not in or near the signaling sequence, however it prevents the
protein from being folded into its proper 3-dimensional structure.
At what point in its route to its destination will the defect be a
problem:
 |
a.
Chaperone interaction in the outer membrane |
 |
b.
Chaperone interaction in the matrix |
 |
c.
Binding to TOM proteins |
 |
d.
Transport through the General Import pore |
 |
e.
Binding to TIM proteins |
Answer: B
2)
The hydrogen pumps on the electron transport chain directly or
indirectly facilitate the following:
 |
a.
Chaperone binding to proteins in the cytoplasm |
 |
b.
Transport through the general import pore |
 |
c.
ADP/ATP Exchange |
 |
d.
Production of ATP |
 |
e.
All of the above |
Answer: E
Last updated:
08/27/03
visitors since 8/09/01
URL:
http://www.cytochemistry.net/cell-biology/mitochondria_Intro.htm
childsgwenv@uams.edu
text © copyright 1996 Gwen V. Childs, Ph.D.
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