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GFP purification

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GFP purification Charles Latrobe College Mariam,Sara,Hoda,Aisha,Kira and Alana. * * * * * * * * * * * * * * * * * What we believed science was These are Quotes from ... – PowerPoint PPT presentation

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Title: GFP purification


1
GFP purification
  • Charles Latrobe College
  • Mariam,Sara,Hoda,Aisha,Kira
  • and Alana.

2
What we believed science was
  • These are Quotes from each student about what
    each thought
  • science is really hard
  • scientists are nerdy
  • scientists are intelligent
  • scientists are smarter than me.

3
How is this project related to a real world
problem?
  • When mitochondria dont function properly it can
    lead to diseases like Huntington and Parkinson
    disease.
  • We use GFP to mark the proteins that are in the
    cells so we can see what they do and how they
    divide, also how they function and how they lead
    to different diseases.

4
What do we mean by integrated science?
  • Integrated science is when you use more than one
    different sciences
  • An example is crystallography, we are trying to
    figure out a biology question while using
    chemistry and physics.
  • Researchers that are interested in biology can
    use chemistry and physics to learn about the
    human body is different ways.

5
The project goal
  • the project goal was to purify the protein GFP.
  • We want to purify proteins so that we can
    crystalize them to determine there structure.
  • We need to know the structure to see how the
    amino acids are important and how the protein
    works.

6
GFP
  • Green Fluorescent Protein (GFP) has existed for
    more than one hundred and sixty million years in
    one species of jellyfish, Aequorea victoria. The
    protein is found in the photo organs of Aequorea

22/06/2015
7
What is GFP used for?
  • GFP is used as a marker to tag proteins so you
    can see them better.

22/06/2015
8
GFP Purification
  • Protocol
  • Resuspend cell pellet
  • Add the aliquot of lysozyme
  • Incubate for 10mins at room temperature
  • We added DNase
  • Incubate for 10 minutes at room temperature
  • Sonicate lysate
  • We separated the soluble fraction and purified
    the protein

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9
GFP Purification
  • Protocol
  • Bind the protein to the Ni-column
  • Wash off all other proteins
  • Then we got back the GFP from the column

22/06/2015
10
GFP Purification
GFP
22/06/2015
11
Microscopic cells
  • You use the blue UV light so you can produce the
    fluorescent colour.
  • The microscope we used was called spinning disc
    microscope.
  • You can change the colour of the UV light if that
    particular colour is in that cell.
  • The green light from the microscope is less
    energetic then the blue light and that is what
    makes the cell green.
  • The red light from the microscope is less
    energetic than the yellow light and thats what
    turns the mitochondria red.

22/06/2015
12
mitochondria
  • We looked at the mitochondria in cells.
  • We saw punta on the mitochondria.
  • We saw that the mitochondria we very dynamic.
  • We saw that the mitochondria moved a lot.
  • If the mitochondria dont move a lot and are
    small, it means the cells are sick.
  • The mitochondria is normally around the nucleus.

22/06/2015
13
Further Areas or Questions to Investigate
  • From the results we gained, we can see that there
    is a need in research for the following
  • How can we see proteins better?
  • How can we explore GFP in other ways?
  • Are there other proteins that are found at the
    mitochondria when they divide?

14
What was interesting about the science that is
happening in this lab?
  • The most interesting part in the science lab was
    using all the different types of equipment and
    the types of buffers.
  • We also looked at the gel under the UV light and
    saw a fluorescent GFP band
  • Viviane showed us the crystalised proteins under
    the microscope

15
Why Should We care about the Research?
  • We should care about research since it plays a
    big part in our everyday life.
  • We need to know more about how the human body
    works.
  • We need to know more about how mitochondria work
    in a cell to keep the energy supply
  • How mitochondria move in a cell is really
    important and when this doesnt work properly,
    diseases can occur

16
How is it relevant to Community and Society?
  • It brings more knowledge to our community
  • We want to know how proteins function in diseases
  • We want to know how the proteins in mitochondria
    affect Huntington disease and Parkinson disease

17
How Has Our View of Science or Scientists Changed?
  • Now that we have a lot more knowledge of what
    scientist do we have a better understanding of
    what they do and how they work in the lab, it has
    changed in a positive manner because we got to
    work in a lab surrounded by them and we realized
    that they work really hard to achieve their goals
    and make the world an healthier environment.

18
What Have We Learnt?
  • Measures and read data accurately
  • Team Work
  • Problem Solving
  • Observation

19
What choices have opened up to me In Possible
Career Choices?
  • We have seen how scientists work in the labs and
    were interested in doing more science
  • We know that you can do science after school
  • And we know that there are several different
    careers in science that allow you to work with
    different types of equipment

20
How has being part of GTP changed my appreciation
for physical science?
  • We now appreciate science a whole lot more
    because we understand what they do for the world,
    and how hard they work in the process, for e.g..
    PhD students who discover new things to make a
    difference.

21
Acknowledgements
  • A special thanks to Viviane Richter our mentor
    for guiding us in the laboratory and helping us
    understand the process of purifying proteins
  • Jill, our career pathways teacher for guiding us
    and helping us get here
  • Eroia, for organizing this experience and giving
    us the opportunity to explore in the lab
  • Prof Mike Ryan, Latrobe university, LIMS
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