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1. Peroxisomal disorders
- Prof. Michael Schrader
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2. Protein import into peroxisomes
- Prof. Michael Schrader
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3. Peroxisomes
- Prof. Michael Schrader
Printable Handouts
Navigable Slide Index
- Introduction
- How do peroxisomes obtain their proteins?
- Transport machineries for peroxisomal matrix and membrane proteins
- Peroxisomal targeting signals (PTS)
- Peroxisomes import fully folded or oligomeric proteins
- PTS and import receptors
- PEX5 and PEX7
- Mammalian peroxisome matrix protein import cycle
- Import of peroxisomal matrix proteins – protein translocation
- Import of peroxisomal matrix proteins – open questions
- Import/insertion of peroxisomal membrane proteins
- Peroxisome biogenesis disorders (PBDs)
- Further reading
- Financial disclosure
Topics Covered
- How peroxisomes obtain their proteins
- Transport machineries for peroxisomal matrix and membrane proteins
- Peroxisomal targeting signals (PTS) and import receptors
- Mammalian peroxisomal matrix protein import cycle
- Mechanism of matrix protein translocation
- Peroxisome biogenesis disorders (PBDs)
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Schrader, M. (2026, May 28). Protein import into peroxisomes [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved August 26, 2026, from https://doi.org/10.69645/AKTL2975.Export Citation (RIS)
Publication History
- Published on May 28, 2026
Financial Disclosures
- Prof. Michael Schrader has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
A selection of talks on Cell Biology
Transcript
Please wait while the transcript is being prepared...
0:00
Welcome, everybody. My
name is Michael Schrader.
I'm a professor of
cell biology in
the Department of Biosciences
at the University of Exeter.
In my short talk, I
would like to explain
protein import into peroxisomes.
0:19
Peroxisomes are
ubiquitous organelles.
We can find them in almost
all eukaryotic cells.
They fulfill very
important functions in
cellular lipid metabolism and
in cellular redox balance.
Peroxisomes in
mammalian cells contain
over 230 proteins, which need
to be targeted to the organ.
The peroxisomal lumen or
so-called matrix is enclosed
by a single limiting membrane.
Peroxisomes do not contain DNA,
therefore all peroxisomal
proteins are encoded in
the nucleus and are translated
on free ribosomes
in the cytoplasm.
The proteins then need to
be post-translationally
transported to the organelle
membrane or matrix.
This requires distinct
transport machineries
for matrix and membrane
protein import.
There are a few examples.
Some peroxisomal
membrane proteins may
be targeted via the
endoplasmic reticulum.
1:27
The molecular
transport machineries
are composed of peroxins.
These are proteins essential
for the biogenesis of
peroxisomes and are
encoded by PEX genes.
They are all numbered
according to their discovery,
and currently more
than 37 peroxins
have been identified
across eukaryotes.
They are usually membrane
proteins or membrane-associated.
The majority of them mediate
matrix protein import.
Three proteins, PEX19, 3,
and 16, are required for
membrane assembly and
membrane protein import.
PEX11 is involved in
the proliferation and
multiplication of peroxisomes,
and dysfunctions in
these peroxins can lead
to severe peroxisome
biogenesis disorders.