BME103:T130 Group 10

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{| style="wikitable" width="700px"
{| style="wikitable" width="700px"
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| [[Image:BME103student.jpg|100px|thumb|Name:<br> '''Jeffery Ramirez'''<br>Role:<br> '''Protocol Planner''']]
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| [[Image:BME103_Group10_JefferyWhyYouNoUploadProfilePic.jpg‎|100px|thumb|Name:<br> '''Jeffery Ramirez'''<br>Role:<br> '''Protocol Planner''']]
| [[Image:BME103_Group10_tylert.jpg|100px|thumb|Name:<br> '''Tyler Tamasauckas''' <br>Role:<br> '''R&D Specialist''']]
| [[Image:BME103_Group10_tylert.jpg|100px|thumb|Name:<br> '''Tyler Tamasauckas''' <br>Role:<br> '''R&D Specialist''']]
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| [[Image:BME103student.jpg|100px|thumb|Name:<br> '''Alexander Baldwin''' <br>Role:<br> '''Open PCR Machine Engineer''']]
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| [[Image:BME103_Group10_AlexWhyYouNoUploadProfilePic.jpg‎|100px|thumb|Name:<br> '''Alexander Baldwin''' <br>Role:<br> '''Open PCR Machine Engineer''']]
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| [[Image:BME103_Group10_FrancesL.jpg|100px|thumb|Name:<br> '''Frances Lakers'''<br>Role:<br> '''R&D Specialist; Data Analyzer''']]
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| [[Image:BME103_Group10_FrancesL.jpg|100px|thumb|Name:<br> '''Frances Lakers'''<br>Role:<br> '''Data Analyzer''']]
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| [[Image:BME103student.jpg|100px|thumb|Name: student<br>Role(s)]]
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|}
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==Initial Machine Testing==
==Initial Machine Testing==
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'''PCR MACHINE'''
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[[Image:OpenPCR1.jpg]]
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1.)'''HOW PCR WORKS'''
1.)'''HOW PCR WORKS'''
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The Polymerase Chain Reaction machine, PCRm for short, works by cycling DNA through different temperatures to amplify the desired strand so the sample can be compared with other DNA. First, the DNA is denatured by heating the samples to such temperature that the hydrogen bonds holding the double-stranded molecule together are broken. The sample is then cooled, which allows a primer to bind to the target DNA. In the third step, the sample is heated back up so an enzyme can replicate the DNA. In the final step, a fluorescent dye binds to the new double-stranded DNA. This process is repeated many times, amplifying the target strand to an analyzable quantity.  
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The Polymerase Chain Reaction machine, PCRm for short, works by cycling DNA through different temperatures to amplify the desired strand so the sample can be compared with other DNA. First, the DNA is denatured by heating the samples to such temperature that the hydrogen bonds holding the double-stranded molecule together are broken. The sample is then cooled, which allows a primer to bind to the target DNA. In the third step, the sample is heated back up so an enzyme, in our case Taq Polymerase, can replicate the DNA. In the final step, a fluorescent dye binds to the new double-stranded DNA. This process is repeated many times, amplifying the target strand to an analyzable quantity.  
    
    
2.)'''STEPS TO AMPLIFY DNA'''
2.)'''STEPS TO AMPLIFY DNA'''
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Step 1. The PCRm lid is heated to 100°C and the sample tubes are heated to 95°C. This temperature is held constant for 3 minutes.
Step 1. The PCRm lid is heated to 100°C and the sample tubes are heated to 95°C. This temperature is held constant for 3 minutes.
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Step 2. The PCRm is then set to run 30 consecutive temperature cycles. Each cycle consists of heating the sample to 95°C for 30 seconds, cooling to 57°C for 30 seconds, and finally, heating to 72°C for 30 seconds.  
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Step 2. The PCRm is then set to run 30 consecutivetemperature cycles. Each cycle consists of heating the sample to 95°C for 30 seconds, cooling to 57°C for 30 seconds, and finally, heating to 72°C for 30 seconds.  
Step 3. After the series of cycles is completed, the PCRm temperature is then held at 72°C for 3 minutes.
Step 3. After the series of cycles is completed, the PCRm temperature is then held at 72°C for 3 minutes.
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Step 4. The PCRm is then kept constant at 4°C
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Step 4. The PCRm is then kept constnt at 4°C
3.)'''COMPONENTS OF PCR MIX'''
3.)'''COMPONENTS OF PCR MIX'''
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The PCR mix consisted of the template DNA, a forward and reverse primer, the GoTaq master mix which is the enzyme, and finally some dH<sub>2</sub>O
4.)'''TABLE OF REAGENTS AND VOLUMES USED'''
4.)'''TABLE OF REAGENTS AND VOLUMES USED'''
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{| {{table}}
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| align="center" style="background:#f0f0f0;"|'''Reagent'''
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| align="center" style="background:#f0f0f0;"|'''Volume'''
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|-
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| Template DNA (20 ng)||0.2μL
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|-
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| 10 μM forward primer||1.0μL
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|-
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| 10 μM reverse primer||1.0μL
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|-
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| GoTaq master mix||50.0μL
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|-
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| dH<sub>2</sub>O||47.8μL
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|-
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| Total||100μL
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|}
5.)'''SAMPLE DESCRIPTIONS'''
5.)'''SAMPLE DESCRIPTIONS'''
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In this lab there were 8 samples that were tested. These samples include a positive control, which has the cancer gene; a negative control, which has no cancer gene and 3 tubes of DNA from two different subjects.
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'''''Fluorimeter Measurements'''''<br>
'''''Fluorimeter Measurements'''''<br>
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1.)'''PHOTO OF SETUP'''
1.)'''PHOTO OF SETUP'''
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[[Image:Fluorimeter.jpg|500px|thumb|]]
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2.)'''STEPS TO ASSEMBLE THE FLUORIMETER'''   
2.)'''STEPS TO ASSEMBLE THE FLUORIMETER'''   
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To assemble the Fluorimeter, there are a few easy steps that need to be followed. The first step is to unbutton the front flaps and open the lid. Take out the interior contents which include the slide that the liquid is put on and the cell phone stand. Once this is done, close the lid so that only the front is open. Place your liquid on the slide, turn on the light and place it inside the box. Then put a cell phone with a camera in the cell phone stand. Align the camera with the drop of liquid on the slide. After this step, the Fluorimeter is set up. Refer to the image above for a photo representation of the set up.
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To assemble the fluorimeter, there are a few easy steps that need to be followed. The first step is to unbutton the front flaps and open the lid. Take out the interior contents which include the slide that the sample is put on and the cell phone stand. Once this is done, close the lid so that only the front is open. Place your sample on the slide, turn on the light and place the entire ensemble inside the box. Then put a cell phone with a camera in the cell phone stand. Align the camera with the sample on the slide. After this step, the fluorimeter is set up. Refer to the image above for a photo of the set up.
3.)'''USING IMAGE J''' <br>
3.)'''USING IMAGE J''' <br>
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We used the program ImageJ to analyze our results. In ImageJ, we first opened the photograph taken using the fluorimeter setup. We then split the photograph into color channels (IMAGE -> COLOR -> SPLIT CHANNELS) in order to separate the "green" of the image from the overall photograph. The SYBRGreen's fluorescence can be analyzed with any expectation of validity only in isolation. The blue and red channel images were disgarded. Before actually measuring the image, we set the desired parameters of measurement (ANALYZE -> SET MEASUREMENTS -> AREA, INTEGRATED DENSITY, MEAN GRAY VALUE). Then, using the "oval" tool, we selected the sample solution in the image. After selecting the sample, we measured for the selected data (ANALYZE -> MEASURE) and recorded the results. Without changing the shape of the selected area, we dragged the oval to be in the background of the image and repeated the measurements. The background numbers are needed to accurately calculate how much of the sample measurements are actually attributed to the sample and not simply the image itself. We repeated this entire process for each photographed sample.
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<br><br>
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'''Primer Development'''<br>
'''Primer Development'''<br>
Normal:
Normal:
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GGAAGTGGGTCCTAAAAACTCTTACA[C/T]TGCATACATAGAAGATCACAGTGGC
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GGAAGTGGGTCCTAAAAACTCTTACA [T] TGCATACATAGAAGATCACAGTGGC
Mutation:
Mutation:
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GGAAGTGGGTCCTAAAAACTCTTACA [C/T] TGCATACATAGAAGATCACAGTGGC
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GGAAGTGGGTCCTAAAAACTCTTACA [C] TGCATACATAGAAGATCACAGTGGC
Forward Primer:
Forward Primer:
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<!--- Place two small Image J data images here. One showing the result of Water and the other showing the result of Calf Thymus DNA --->
<!--- Place two small Image J data images here. One showing the result of Water and the other showing the result of Calf Thymus DNA --->
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[[Image:BME103_Group10_Water_Green.jpg‎|300px|thumb|Green channel from photograph of water sample.]]
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[[Image:BME103_Group10_Thymus_Green.jpg|300px|thumb|Green channel from photograph of Calf Thymus DNA sample.]]
<!--- Enter the values from your group's Data Analyzer table below. E6, F6, etc. are the excel cells from which you should copy your data. --->
<!--- Enter the values from your group's Data Analyzer table below. E6, F6, etc. are the excel cells from which you should copy your data. --->
{| {{table}}
{| {{table}}
|- style="background:#f0f0f0;"
|- style="background:#f0f0f0;"
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| '''Sample''' || '''Integrated Density''' || '''DNA μg/mL''' || '''Conclusion'''
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| '''Sample''' || '''Net Integrated Density (Image-Background)''' || '''DNA μg/mL''' || '''Conclusion'''
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| PCR: Negative Control || 2700889 || 0.576 || Negative
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| PCR: Positive Control || 3481893 || 0.743 || Positive
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| PCR: Negative Control || E6 || F6 || G6
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| PCR: Calf Thymus || 9372391 || 2 || Positive
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| PCR: Positive Control || E7 || F7 || G7
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| PCR: Water || 7193042 || 0 || Negative (No Signal)
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| PCR: Patient 1 ID #####, rep 1 || E8 || F8 || G8
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| PCR: Patient 1 ID 92986, rep 1 || 6917330 || 1.476 || Negative
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| PCR: Patient 1 ID #####, rep 2 || E9 || F9 || G9
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| PCR: Patient 1 ID 92986, rep 2 || 18548291 || 3.958 || Positive
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| PCR: Patient 1 ID #####, rep 3 || E10 || F10 || G10
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| PCR: Patient 1 ID 92986, rep 3 || 9971894 || 2.128 || Positive
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| PCR: Patient 2 ID #####, rep 1 || E11 || F11 || G11
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| PCR: Patient 2 ID 81682, rep 1 || 766751 || 0.164 || Negative (No Signal)
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| PCR: Patient 2 ID #####, rep 2 || E12 || F12 || G12
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| PCR: Patient 2 ID 81682, rep 2 || 6144131 || 1.311 || Negative
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| PCR: Patient 2 ID #####, rep 3 || E13 || F13 || G13
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| PCR: Patient 2 ID 81682, rep 3 || 7734546 || 1.650 || Positive
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|}
KEY
KEY
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* '''Sample''' = <!--- explain what "sample" means --->
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* '''Sample''' = The specific genetic material used in that trial. For example, the three trials labeled Patient 1 used DNA from that patient and that patient only.<!--- explain what "sample" means --->
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* '''Integrated Density''' = <!--- explain what "integrated density" means and how you did background subtraction to get this value --->  
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* '''Integrated Density''' = The sum of the values of the pixels in the sample image area. Also equivalent to product of the Mean Gray Value and the Area. The above values represent the integrated density after removing the "background noise" of the image's background pixel values. In math terms, Net IntDen = (IntDen Sample) - (IntDen Background)<!--- explain what "integrated density" means and how you did background subtraction to get this value --->  
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* '''DNA μg/mL''' = <!--- explain how you calculated this --->  
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* '''DNA μg/mL''' = Amount of genetic material present within sample. This was calculated using a proportional equation. Given that the Calf Thymus sample contained 2μg/mL, we were able to set up this equation for estimating the amount of genetic material present in the unknown samples. <br>(Sample)μg/mL = (IntDen Sample)*[(2μg/mL)/(IntDen Calf Thymus)]<!--- explain how you calculated this --->  
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* '''Conclusion''' = <!--- explain what "Positive" and "No signal" means, relative to the control samples --->
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* '''Conclusion''' = Our conclusion as to whether or not the sample genetic material contains the polymorphism for cancer. A "Positive" conclusion indicates a likelihood of the cancerous polymorphism being present while a "Negative" or "No Signal" conclusion indicates a likelihood of the polymorphism's absence. These conclusions were mainly drawn based on the visual fluorescence of the samples and supported by the amount of genetic material present.<!--- explain what "Positive" and "No signal" means, relative to the control samples --->

Current revision

BME 103 Fall 2012 Home
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Contents

OUR TEAM

Name: Jeffery RamirezRole: Protocol Planner
Name:
Jeffery Ramirez
Role:
Protocol Planner
Name: Tyler Tamasauckas Role: R&D Specialist
Name:
Tyler Tamasauckas
Role:
R&D Specialist
Name: Alexander Baldwin Role: Open PCR Machine Engineer
Name:
Alexander Baldwin
Role:
Open PCR Machine Engineer
Name: Frances LakersRole: Data Analyzer
Name:
Frances Lakers
Role:
Data Analyzer

LAB 1 WRITE-UP

Initial Machine Testing

PCR MACHINE

Image:OpenPCR1.jpg



The Original Design
(Add image of the full OpenPCR machine here, from the Week 3 exercise. Write a paragraph description for visitors who have no idea what this is)
The OpenPCR machine is designed to isolate and replicate certain sequences of DNA through heating and cooling the samples. There are several parts to it, most of which can only be seen if one of the outside walls is taken out. The samples of DNA are placed in small tubes and are then placed in the heating area, where they are repeatedly heated and cooled during several cycles to achieve the desired result. The time for a cycle is usually a few minutes, and there are usually several cycles in a run, so it may last over an hour.

Experimenting With the Connections

When the circuit board (part 6) was unplugged from the display (part 3), the display turned off and no longer registered any signal. The display was no longer functional, but turned on again once the wire between the two parts was reconnected.

When the circuit board was unplugged from the heating element, the heating element was no longer able to control its temperature. Although it still had power, it was not being controlled by the circuit board.


Test Run

The first test run completed on the OpenPCR machine was on October 25, 2012. The test was successful, and was completed in roughly the time expected, give or take a few minutes. Once the settings were put to the correct levels, the set up was quite simple. The samples were placed inside the heating unit, then the test run started. It took over an hour, but was completed successfully with no malfunctioning pieces of equipment.




Protocols

Polymerase Chain Reaction

1.)HOW PCR WORKS

The Polymerase Chain Reaction machine, PCRm for short, works by cycling DNA through different temperatures to amplify the desired strand so the sample can be compared with other DNA. First, the DNA is denatured by heating the samples to such temperature that the hydrogen bonds holding the double-stranded molecule together are broken. The sample is then cooled, which allows a primer to bind to the target DNA. In the third step, the sample is heated back up so an enzyme, in our case Taq Polymerase, can replicate the DNA. In the final step, a fluorescent dye binds to the new double-stranded DNA. This process is repeated many times, amplifying the target strand to an analyzable quantity.

2.)STEPS TO AMPLIFY DNA

The actual steps for PCR are quite simple.

Step 1. The PCRm lid is heated to 100°C and the sample tubes are heated to 95°C. This temperature is held constant for 3 minutes.

Step 2. The PCRm is then set to run 30 consecutivetemperature cycles. Each cycle consists of heating the sample to 95°C for 30 seconds, cooling to 57°C for 30 seconds, and finally, heating to 72°C for 30 seconds.

Step 3. After the series of cycles is completed, the PCRm temperature is then held at 72°C for 3 minutes.

Step 4. The PCRm is then kept constnt at 4°C

3.)COMPONENTS OF PCR MIX

The PCR mix consisted of the template DNA, a forward and reverse primer, the GoTaq master mix which is the enzyme, and finally some dH2O

4.)TABLE OF REAGENTS AND VOLUMES USED

Reagent Volume
Template DNA (20 ng)0.2μL
10 μM forward primer1.0μL
10 μM reverse primer1.0μL
GoTaq master mix50.0μL
dH2O47.8μL
Total100μL

5.)SAMPLE DESCRIPTIONS

In this lab there were 8 samples that were tested. These samples include a positive control, which has the cancer gene; a negative control, which has no cancer gene and 3 tubes of DNA from two different subjects.


Fluorimeter Measurements


1.)PHOTO OF SETUP
















2.)STEPS TO ASSEMBLE THE FLUORIMETER

To assemble the fluorimeter, there are a few easy steps that need to be followed. The first step is to unbutton the front flaps and open the lid. Take out the interior contents which include the slide that the sample is put on and the cell phone stand. Once this is done, close the lid so that only the front is open. Place your sample on the slide, turn on the light and place the entire ensemble inside the box. Then put a cell phone with a camera in the cell phone stand. Align the camera with the sample on the slide. After this step, the fluorimeter is set up. Refer to the image above for a photo of the set up.

3.)USING IMAGE J

We used the program ImageJ to analyze our results. In ImageJ, we first opened the photograph taken using the fluorimeter setup. We then split the photograph into color channels (IMAGE -> COLOR -> SPLIT CHANNELS) in order to separate the "green" of the image from the overall photograph. The SYBRGreen's fluorescence can be analyzed with any expectation of validity only in isolation. The blue and red channel images were disgarded. Before actually measuring the image, we set the desired parameters of measurement (ANALYZE -> SET MEASUREMENTS -> AREA, INTEGRATED DENSITY, MEAN GRAY VALUE). Then, using the "oval" tool, we selected the sample solution in the image. After selecting the sample, we measured for the selected data (ANALYZE -> MEASURE) and recorded the results. Without changing the shape of the selected area, we dragged the oval to be in the background of the image and repeated the measurements. The background numbers are needed to accurately calculate how much of the sample measurements are actually attributed to the sample and not simply the image itself. We repeated this entire process for each photographed sample.



Research and Development

Specific Cancer Marker Detection - The Underlying Technology

This exercise primarily uses the Polymerase Chain Reaction (PCR) method to replicate and amplify explicit DNA sequences that could be used to identify susceptibility to cancer and other diseases. During the process, this experiment uses a combination of a sample of Template DNA, DNA Primers, Taq Polymerase and thermocycling preformed by a PCR machine. After combining the sample DNA and chemicals, the sample tubes are placed into the OpenPCR machine where they will undergo the amplification process. The PCR process begins by heating the samples to break apart the matched strands of DNA. The result is two separate DNA molecules. The PCR machine then reduces the temperature in order to allow the pre-specified primers to bind to the intended region on the strand of DNA. After reheating the sample solution, Taq Polymerase is able to take base pairs and re-synthesize the paired strands. The process is repeated a total of 30 to 35 times, but by the third heat cycle we are able to produce the specific DNA sequence without any extra sequences.

The specific rs17879961[1] used in our exercise has been related to Breast Cancer, Li-Fraumeni syndrome and other cancers [2]. The rs17879961 is a mutation specific to the CHEK2 gene, which relates to a cell's ability to fix DNA when any damage occurs. The rs17879961 mutation would allow for increased susceptibility to cancer. In the field, PCR and the use of the specific primers would allow for the rapid replication of the the gene, should the mutation be present. However, if the mutation did not exist in the patient the replication would occur on a significantly smaller scale.

Example Animation

Image:BME103_Group10_PCRbyTyler.gif

Primer Development
Normal: GGAAGTGGGTCCTAAAAACTCTTACA [T] TGCATACATAGAAGATCACAGTGGC

Mutation: GGAAGTGGGTCCTAAAAACTCTTACA [C] TGCATACATAGAAGATCACAGTGGC

Forward Primer:

CCTTCACCCAGGATTTTTGAG

Backward Primer:

ATGTATCTTCTAGTGTCACCG

Bayes Rule (A test of Reliability)

Bayes Rule allows us to calculate the probability that a positive result actually has cancer present in the patient

P(A|B) = \frac{P(B | A)\, P(A)}{P(B)} \,




Results

Green channel from photograph of water sample.
Green channel from photograph of water sample.
Green channel from photograph of Calf Thymus DNA sample.
Green channel from photograph of Calf Thymus DNA sample.
Sample Net Integrated Density (Image-Background) DNA μg/mL Conclusion
PCR: Negative Control 2700889 0.576 Negative
PCR: Positive Control 3481893 0.743 Positive
PCR: Calf Thymus 9372391 2 Positive
PCR: Water 7193042 0 Negative (No Signal)
PCR: Patient 1 ID 92986, rep 1 6917330 1.476 Negative
PCR: Patient 1 ID 92986, rep 2 18548291 3.958 Positive
PCR: Patient 1 ID 92986, rep 3 9971894 2.128 Positive
PCR: Patient 2 ID 81682, rep 1 766751 0.164 Negative (No Signal)
PCR: Patient 2 ID 81682, rep 2 6144131 1.311 Negative
PCR: Patient 2 ID 81682, rep 3 7734546 1.650 Positive


KEY

  • Sample = The specific genetic material used in that trial. For example, the three trials labeled Patient 1 used DNA from that patient and that patient only.
  • Integrated Density = The sum of the values of the pixels in the sample image area. Also equivalent to product of the Mean Gray Value and the Area. The above values represent the integrated density after removing the "background noise" of the image's background pixel values. In math terms, Net IntDen = (IntDen Sample) - (IntDen Background)
  • DNA μg/mL = Amount of genetic material present within sample. This was calculated using a proportional equation. Given that the Calf Thymus sample contained 2μg/mL, we were able to set up this equation for estimating the amount of genetic material present in the unknown samples.
    (Sample)μg/mL = (IntDen Sample)*[(2μg/mL)/(IntDen Calf Thymus)]
  • Conclusion = Our conclusion as to whether or not the sample genetic material contains the polymorphism for cancer. A "Positive" conclusion indicates a likelihood of the cancerous polymorphism being present while a "Negative" or "No Signal" conclusion indicates a likelihood of the polymorphism's absence. These conclusions were mainly drawn based on the visual fluorescence of the samples and supported by the amount of genetic material present.


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