A cancer drug exploration

Slides:



Advertisements
Similar presentations
PURIFICATION OF GFP USING HIC CHROMATOGRAPHY. Chromatography  A technique used to separate molecules based on how they tend to cling to or dissolve in.
Advertisements

LABORATORY 6: PURIFYING THE FLUORESCENT PROTEIN 2014.
LABORATORY 6 PART B PURIFICATION OF M FP FROM AN OVERNIGHT CULTURE.
pGLO ™ & GFP Stan Hitomi Director, Edward Teller Education Center UC Davis / Lawrence Livermore National Laboratory, Livermore, CA Kirk Brown Lead Instructor,
Griffith ’ s Mysterious Transformation Experiment.
pGLO™ Transformation and Purification of
STREAKING AN AGAR PLATE FOR ISOLATIONOF BACTERIAL COLONIES BACTERIAL COLONIES.
pGLO™ Transformation and Purification of
Protein is Cash: Biomanufacturing in High School Classrooms
Protein Purification. What do you know about proteins? Why do we need to purify proteins? What are you curious about?
Genetic engineering ­ Genetic engineering: manipulating DNA or organisms to perform practical tasks or provide useful products We’re going to look at the.
PGLO™ & GFP.
Bacterial Transformation
Green Fluorescent Protein (GFP) Purification by Chromatography
GFP Transformation Lab Images taken without permission from
Genetic Engineering changing DNA within an organism.
Recombinant DNA.
Green Fluorescent Protein: A Reporter Molecule
Learning Targets “I Can...” -Explain what it means for a gene to be expressed. -Explain the role of plasmids. -Define bacteria “transformation.” -Insert.
Developing A Protein Purification Protocol Billie Parker
Green Fluorescent Protein (GFP) Purificaiton. Recombinant Cell.
Learning Targets “I Can...” -Explain what it means for a gene to be expressed. -Explain the role of plasmids. -Insert a plasmid into bacteria to observe.
Bacterial Art and GFP Nick Slawson.
Chapter 20 Experimental Systems Dr. Capers.  In vivo ○ Involve whole animal  In vitro ○ Defined populations of immune cells are studied under controlled.
Introduction to pGLO lab Bacteria Transformation Please take these notes carefully. You do not need to write anything in RED.
PGLO Bacterial Transformation, Purification and SDS gel.
4-2 Sources of DNA.
Is taking in a plasmid good or bad for the bacteria? Explain.
Biology Technology: the application of scientific advances to benefit humanity Biotechnology: The use of living organisms or their products.
Laboratory Procedure for bacterial transformation with pGLO It’s glowing.
Lab 10- Colony isolation Mixed culture and unknown.
Hey Kim, this site shows the kids everything! NY ‘09 use this for the prelab stuff!! Michael.Gregory/files/Bio%20100/Bio%
Purification of Green Fluorescent Protein (GFP) Stan Hitomi Coordinator – Math & Science Principal – Alamo School San Ramon Valley Unified School District.
EDS 198 ADAPTING LABS FOR INQUIRY.  Lab Review and Analysis of Results  Adapting Lab for Inquiry  Protein Purification Lab Background AGENDA.
QoD (HB)  Do you remember what a plasmid is?
Intended Learning Objectives You should be able to… 1. Give 3 examples of proteins that are important to humans and are currently produced by transgenic.
DNA Technology Part 2.
Treatments that stimulate the E.coli. to take up foreign plasmids include: 1.CaCL2 treatment 2.Heat shock 3.Incubation with ECORI 4.1 and and 3 6.All.
In the pGLO lab, we will: Use recombinant DNA Genetically engineer E. coli bacteria by inserting a plasmid Plate and grow bacteria Determine if the proteins.
Genetic Engineering and Gene Regulation. What is genetic engineering? Manually adding new DNA to an organism, giving an organism traits it wouldn’t naturally.
Bacterial Transformation Lab
Genetic Transformation of Bacteria and Gene Regulation.
GENETIC TRANSFORMATION. WHAT IS GENETIC TRANSFORMATION Genetic transformation is altering a cell by adding genetic information from an outside source.
pGLO™ Transformation and Purification of Green Fluorescent Protein (GFP)
In the pGLO lab, we will: Use recombinant DNA Genetically engineer E. coli bacteria by inserting a plasmid Plate and grow bacteria Determine if the proteins.
pGLO™ Transformation and Purification of Green Fluorescent Protein (GFP)
pGLO™ Transformation and Purification of
PGLO™ & GFP. pGLO™ & GFP pGLO™ Transformation and Purification of Green Fluorescent Protein (GFP) Instructors Stan Hitomi Director, Edward Teller.
GFP Transformation Lab
Purification of Green Fluorescent Protein
DNA Technology Part 2.
Fac. of Agriculture, Assiut Univ.
Lab 7 – Purification of RFP protein (mFP) from an overnight culture
Protein Structure and Analysis
Pre-Lab: pGLO Bacterial Transformation
Secrets of the rainforest
Genetic Transformation of Bacteria and Gene Regulation
Protein Production Jackpot!
Lab 8 Warm-Up What are plasmids?
Bacterial Transformation
Lab 8 Warm-Up What are plasmids?
Purification of mFP from an overnight culture
Jeopardy Final Jeopardy Unit 1- Unit 2- Unit 3- Unit 4- Lagniape $100
Introduction to the pGLO Lab
pGLO™ Transformation and Purification of
Streaking an Agar Plate For
Downstream Processing
Purification of Green Fluorescent Protein
GFP Transformation Lab
Presentation transcript:

A cancer drug exploration Secrets of the Rainforest A cancer drug exploration

The Mysterious Green Florescent Leaves Hi, I am Tisha While Hiking through the Andean Rain Forest, You and a friend, Tisha, obtain medicinal green leaves from Ramon You bring back to Biotex, a biotech company working on a cure for cancer

Green Florescent Protein Biotex scientists determine that the leaves contain a florescent green protein DNA from the leaves is inserted into bacterial cells

Cloning the Gene from Mysterious Leaves

More on Cloning the Gene…

Purifying the GFP Biotex technicians need to separate the GFP from other bacterial proteins Column Chromatography separates contaminating proteins from GFP The result is a purified GFP that can be tested for its ability to cure stomach cancer

Testing and Placebos GFP will need to be tested on rats before it is allowed for a human trial The US Food and Drug Administration will examine Biotex’s experiments to determine if the protein is safe and cures stomach cancer without negative side effects

Ethics and Economics Once GFP is approved by the FDA, you will develop GFP as a commercial product You will need to be aware of the following viewpoints: FDA, social conscience, patient advocacy groups, and the employees of Biotex You must resolve the dilemmas in order to successfully market GFP

Final Presentations Turn in all lab work with analysis questions Video Presentation of your marketing of GFP Address issues of all dilemmas 1-8

Background Information- Lesson 1 How to use Pipettes Streaking of agar plates to Produce Single Colonies (Sterile Technique)

Background Continued…Lessons 2 & 3 Process of Transformation (GMOs or genetic recombinants) Jellyfish , GFP and pGLO and Fluorescence Isolating Clones to Propagate in Liquid Culture Media

Background Continued…Lesson 4 Concentration of Bacteria from Liquid Culture Media

Background Continued…Lesson 5 Prepare a Bacterial Lysate for Protein Chromatography

Background Continued…Lesson 6 Protein Chromatography- Hydrophobic Interaction Chromatography (HIC) GFP is hydrophobic and will stick to hydrophobic beads in salt water buffer When salt is removed, GFP will then be collected 4 buffers: 1) Equilibration buffer (salt buffer) 2) Binding Buffer (high salt) Wash buffer (medium salt) Elution buffer (low salt)

Background Continued…Lessons 7-10 Lesson 7- testing and placebos Lesson 8- Advocacy Groups and Viewpoints Lesson 9-Ethics and Economics Lesson 10- Preparing and Giving Presentations