BME103:T130 Group 1

BME 103 Fall 2012	Home People Lab Write-Up 1 Lab Write-Up 2 Lab Write-Up 3 Course Logistics For Instructors Photos Wiki Editing Help
OUR TEAM Name: Tianzhu Zhu Experimental protocol planner Name: Wyatt Hansen Open PCR machine engineer Name: Bryce Hicok Open PCR machine engineer Name: Jesus Ibarra Experimental protocol planner Name: Emma Maiorella R&D scientist LAB 1 WRITE-UP Initial Machine Testing The Original Design The OpenPCR runs from your computer and connects through your USB port. You can add and delete steps, edit temperatures, and create thermocycler protocols from your computer. Experimenting With the Connections - When the PCB board of LCD is unlplugged from the Circuit Board, the LCD goes off. - When the white wire connecting the circuit board to the heat plate, the LCD showed an incorrect reading of the temperature. Test Run Our First practice run was conducted on October 25th, 2012. Our experience with the open PCR went smoothly. The test run took approximately one hour and forty five minutes. It was easy to set up and begin a test run. The only trouble we ran into was when adjusting the heat lid it was hard to tell when the lid was tightened down enough and it if very easy to tighten it too much and squish the test tubes in the PCR. Protocols Polymerase Chain Reaction Polymerase Chain Reaction is the process of rapid duplication of a strand of DNA. The process first requires a DNA template, which contains the strand of DNA that is intended to be copied multiple times. The template strand is then been heated in order to separate the double stranded DNA and DNA Polymerase is added in order to create a strand of DNA that is complimentary to the original intended DNA strand, which creates a primer. Then the temperature is lowered so that the nucleotides will bind together in complementary to the primers in order to create a copy of the targeted DNA strand. The heating and cooling process will be repeated over a period of approximately 2 hours in order to create a large amount of DNA strand copies. Steps to amplify DNA 1.) Collect a blood sample from the patient. 2.) Use chemicals and centrifuge to separate the DNA materials from the rest of the blood components. 3.) Apply heat (95 degree Celsius) for 3 minutes to the DNA strand to separate the double stranded DNA into 2 single strands. 4.) In stage two, there are 35 cycles which consists of 95 degree Celsius for 30 seconds. 5.) Add primers and cool (57 degree Celsius, then 72 degree Celsius) the sample to allow the primers to bind to the separated original DNA strands. 6.) Then reheat the samples again to separated the resulting replicated strands. 7.) Add primers and cool the samples again. 8.) Repeat the process of heating and cooling in order for the primers to bind to all the separated DNA strands. 9.) Over the course of 2 hours or so, there will be a large amount of duplicated DNA strands. For a 25μL reaction volume components volume Final conc GoTaq® Colorless Master Mix, 2X 12.5µl 1X upstream primer,10µM 0.25–2.5µl 0.1–1.0µM downstream primer, 10µM 0.25–2.5µl 0.1–1.0µM DNA template 1–5µl <250ng Nuclease-Free Water to 25µl N.A For a 50μL reaction volume components volume Final conc GoTaq® Colorless Master Mix, 2X 25.0µl 1X upstream primer,10µM 0.50-5.0µl 0.1–1.0µM downstream primer, 10µM 0.50–5.0µl 0.1–1.0µM DNA template 1–5µl <250ng Nuclease-Free Water to 50µl N.A For a 100μL reaction volume components volume Final conc GoTaq® Colorless Master Mix, 2X 50.0µl 1X upstream primer,10µM 1.00–10.0µl 0.1–1.0µM downstream primer, 10µM 1.00–10.0µl 0.1–1.0µM DNA template 1–5µl <250ng Nuclease-Free Water to 100µl N.A all credit goes to: http://www.promega.com/resources/protocols/product-information-sheets/g/gotaq-colorless-master-mix-m714-protocol/ Flourimeter Measurements Procedures for Fluorimeter Assembly: 1.)Place glass slide down on fluorimeter. 2.)Place a drop of water on the slide then another close by to form one large drop. 3.)Turn on light so that it may pass through water drop. 4.)Move the system into the black box. 5.)Place smart phone in stand. 6.)Take picture and record image. Research and Development Specific Cancer Marker Detection - The Underlying Technology There are many factors that contribute to a PCR reaction. First, a sample of DNA from a patient must be extracted. This sample is called template DNA. During the reaction, primers, or artifically synthesized bits of DNA, bind to the target sequence if it is present in the DNA. The enzyme taq polymerase's job is to regenerate the DNA strand that was melted away. Magnesium chloride (MgCl2) binds to the taq polymerase protein as a cofactor to help it function properly. In addition, there are dNTP's floating around in the solution of DNA. These deoxynucleotidetriphosphates are the bases (A,T,C,G) ready to be bound by the taq polymerase enzyme. During a PCR reaction, the solution of DNA is first heated to a temperature of 95 degrees Celsius to essentially melt the hydrogen bonds between the bases on the double strand of DNA. Next, the solution is cooled down to 57 degrees Celsius so the primers can bind to the target sequence of the DNA if it is present. Finally, the solution is heated up to 72 degrees Celsius, where polymerization occurs. This process of heating and cooling is repeated for a total of 34 cycles. This will ensure that the DNA has been amplified enough so it is able to be seen when a flourescent solution is added. Since the primers will not bind to the DNA if the target sequence is not present, a non-cancer patient will produce a negative result. This is because instead of having millions of double stranded DNA in the solution, the solution will only contain single strands. The specific cancer-associated gene sequence being analyzed is the r17879961 SNP. The mutation is present at position number 29,121,087 in the DNA. The "ATT" sequence in a non-cancer human is replaced by the "ACT" sequence. Therefore, during a PCR reaction, primers will bind to the sequence, "ACT", since it is the cancer gene. This image shows what happens to the DNA strand each time it replicates. First, the bonds are melted and separated. Then, primers attach themselves to each end of the DNA strand. Next, taq polymerase adds the appropriate bases to create a new piece of double-stranded DNA. Finally, this process is repeated for approximately 30 cycles. Image borrowed from: [1] Results ImageJ Software Processing Sample Image or Background Area INTDEN RAWINTDEN Negative Image 101 78380 45.989 3604632 Negative Background 101 78380 1.215 95224 Patient 2 Image 102 82228 44.098 3626088 Patient 2 Background 102 82228 .896 73708 Patient 2 Image 103 80244 65.783 5278725 Patient 2 Background 103 80244 .777 62338 Patient 2 Image 104 90368 37.274 3368381 Patient 2 Background 104 90368 2.346 211974 DNA Calf Thymus & Sybrgreen Image 105 99512 181.282 18039714 DNA Calf Thymus & Sybrgreen Background 105 99512 1.786 177715 Positive Image 106 111476 191.028 21295059 Positive Background 106 111476 .912 101693 Patient 1 Image 107 88468 224.745 19882762 Patient 1 Background 107 88468 2.026 179269 Patient 1 Image 108 68088 .953 64894 Patient 1 Background 108 68088 .953 64894 Patient 1 Image 109 109904 195.414 21476774 Patient 1 Background 109 109904 1.335 146762 Water Image 110 69680 95.314 6641513 Water Background 110 69680 1.981 138023 Sample Integrated Density DNA μg/mL Conclusion PCR: Negative Control E6 F6 G6 PCR: Positive Control E7 F7 G7 PCR: Patient 1 ID 48199, rep 1 E8 F8 G8 PCR: Patient 1 ID 48199, rep 2 E9 F9 G9 PCR: Patient 1 ID 48199, rep 3 E10 F10 G10 PCR: Patient 2 ID 15130, rep 1 E11 F11 G11 PCR: Patient 2 ID 15130, rep 2 E12 F12 G12 PCR: Patient 2 ID 15130, rep 3 E13 F13 G13 KEY Sample = The sample is the substance tested using the flourimeter, in the case of this lab the substances used are a positive control, negative control, 3 trials for patient one, and 3 trials for patient 2. Integrated Density = Integrated density is the sum of the pixels in a given are, this is found by finding the product of the are and mean gray value then subtracting the background. DNA μg/mL = This is the concentration of DNA in the respective sample, this is calculated by multiplying the integrated density by 2 and dividing by the integrated density value of calf thymus. Conclusion = A positive signal represents a sample that exhibited the same reaction to sybr green in the lab as our positive control; a negative signal represents a sample that exhibited the same reaction to sybr green as the negative control.