Difference between revisions of "20.109(F21):M1D4"

From Course Wiki
Jump to: navigation, search
(Navigation links)
(Part 3: Perform CometChip experiment)
Line 54: Line 54:
#For each As treatment concentration, harvest and pellet 2 M cells by centrifuging at 200 g for 5 min at room temperature.
#For each As treatment concentration, harvest and pellet 2 M cells by centrifuging at 200 g for 5 min at room temperature.
#Prepare 2 μM and 10 μM As treatment concentrations in media.
#Prepare 2 μM As treatment concentrations in media.
#Resuspend each cell pellet in 6 mL of the As-containing media.
#Resuspend each cell pellet in 6 mL of the As-containing media.
#Transfer cell suspensions to fresh T25 flasks and incubate at 37 °C for 24 hrs.
#Transfer cell suspensions to fresh T25 flasks and incubate at 37 °C for 24 hrs.

Revision as of 19:59, 17 September 2021

20.109(F21): Laboratory Fundamentals of Biological Engineering
Drawing provided by Marissa A., 20.109 student in Sp21 term.  Schematic generated using BioRender.

Fall 2021 schedule        FYI        Assignments        Homework        Class data        Communication        Accessibility

       Module 1: Genomic instability                          Module 2: Drug discovery       


For the next experiment in this module you will use the CometChip assay developed in the Engelward Laboratory. The CometChip assay is used to assess various types of DNA lesions, including base excisions, abasic sites, strand breaks, and crosslinks.

Microscopy images showing results from CometChip assay. A. In the CometChip assay DNA damage is measured by determining the amount of DNA in the head versus the tail of the comet. B. Cells not treated with DNA damaging agent (left) have visibly less DNA damage that cells treated with DNA damaging agent (right) as evidenced by the amount of DNA in the tail.
To measure DNA damage, the CometChip assay relies on gel electrophoresis. Electrophoresis is a technique used to separate molecules by size using an applied electrical field and a sieving matrix. DNA, RNA and proteins are often studied with this technique; agarose and acrylamide gels are the two most common sieves. The molecules to be separated enter the matrix through a well at one end and are pulled through the matrix when a current is applied. Because DNA and RNA are negatively charged molecules due to their phosphate backbone, they naturally travel toward the positive charge at the far end of the gel. Larger molecules are entwined in the matrix and are stalled; smaller molecules wind through the matrix more easily and travel further from the well. Over time fragments of similar length accumulate into 'bands' in the gel. The CometChip assay is based upon the principle that damaged DNA travels more readily compared to undamaged DNA.

In the CometChip assay, cells are loaded into microwells that are 'stamped' onto an agarose gel sieving matrix. Specific treatments can then be applied to the cells within these microwells that induce DNA damage. The cells are then lysed to release the DNA into the microwell. Following cell lysis, the CometChip is incubated in an alkaline buffer that unwinds the DNA. This step allows for all types of DNA damage to be detected. Lastly, gel electrophoresis is used to separate the DNA fragments. DNA fragments migrate away from the microwell and generate a comet tail as shown in the image to the right (panel A). The distance that the DNA migrates (i.e. the length of the comet tail) is proportional to the amount of damage. For example, with cells not treated with a DNA damaging agent, there are no evident comet tails to the right of the microwell or 'head' (panel B, image on the left); however, in cells treated with a DNA damaging agent there are comet tails apparent (panel B, image on the right). Comet tail lengths can be compared across experimental treatments to determine the deleterious effects of chemicals and toxins on DNA stability. In addition, the CometChip assay can be used to study the rate and efficiency of repair in response to specific treatments.


Part 1: Learn about the CometChip

As discussed in the prelab lecture, you will use two methods to assess DNA damage: the γH2AX assay and the CometChip. Before we review the CometChip experimental details, it is best to familiarize yourself with the procedure and assay.

Read the Abstract and Introduction in the following publication:

CometChip: A high-throughput 96-well platform for measuring DNA damage in microarrayed human cells. Journal of Visualized Experiments. (2014) 92: 1-11.

In your laboratory notebook, answer the following questions:

  • Why is it important to study DNA damage?
    • You can consider the information provided in lecture / prelab to answer this question.
  • How does the CometChip estimate the level of DNA damage within cells?
  • List two issues / problems with the comet assay?
  • List two improvements provided by the CometChip assay?

Part 2: Prepare CometChip

Image of CometChip showing distinction between (A) 'macrowell' and (B) 'microwell'.
The CometChip is simply a thin layer of agarose with microwells. It is important to differentiate between the terms 'macrowell' and 'microwell' for your experiments. A bottomless 96-well plate is placed on top of the agarose CometChip to create the macrowells for the CometChip assay (panel A). This enables researchers to control which cells are exposed to which treatment. The microwells were stamped into the agarose when you made your CometChip (panel B). Within each well are ~ 300 microwells, which are ~40 μm in diameter and 40 μm in depth.

To ensure the steps required for preparing a CometChip are clear, the Instructor will provide a live demonstration of this process. You should provide a written description of the procedure in your laboratory notebook!

In your laboratory notebook, complete the following:

  • Provide a written overview / description of the the procedure used to prepare a CometChip (from the live demonstration).
  • Onto which side of the GelBond is the agarose poured to make a CometChip?
  • How are the microwells generated in the agarose of the CometChip?

In addition, a video demonstrating the finishing procedure to make a CometChip is linked here: Making the CometChip

Part 3: Perform CometChip experiment

As with the γH2AX experiment, the MCL-5 cells with be treated with H2O2 +/- As exposure. The treatments will be applied in two parts. First, cells will be incubated in As for 24 hrs to mimic exposure to the toxic metal. Second, the cells will be incubated in H2O2 for 20 min to induce DNA damage. Following treatment with H2O2 the cells will be visualized to assess DNA repair.

To ensure the steps included below are clear, please watch the video tutorial (linked here). The steps are detailed below so you can follow along! Please note that the video shows the general steps for completing an experiment using the CometChip assay. The specific procedure used to generate the data you will analyze are written below. Furthermore, the video shows two version of the CometChip assay: the alkaline and the neutral. In this module, the alkaline CometChip assay was used.

Expose cells to As
Due to the timing of the As treatment, the Instructors completed the below steps using the cells that you seeded in the T75 flasks during the previous laboratory session. Using the As treated cells you will complete the steps starting at Load cells into CometChip.

  1. For each As treatment concentration, harvest and pellet 2 M cells by centrifuging at 200 g for 5 min at room temperature.
  2. Prepare 2 μM As treatment concentrations in media.
  3. Resuspend each cell pellet in 6 mL of the As-containing media.
  4. Transfer cell suspensions to fresh T25 flasks and incubate at 37 °C for 24 hrs.

Load cells into CometChip

  1. Remove your CometChip from the 1x PBS and place it, gelbond side down, on the glass plate.
    Binder clip placement for CometChip sandwich.
  2. Press the 96-well bottomless plate upside-down onto the CometChip.
    • Be sure to press the top of the 96-well bottomless plate onto the CometChip.
    • Do not move the 96-well bottomless plate while it is on the CometChip as you will damage the agarose and the microwells.
  3. Use the binder clips to secure the 96-well bottomless plate to the glass plate, thus creating a 'sandwich' with your CometChip in the center.
    • Fasten the binder clips to the very edge of 96-well bottomless plate as shown in the image to the right.
  4. Calculate the volume of cell suspension that contains 25,000 cells given the density of the cell suspension is 500,000 cells / mL.
  5. Add the volume of cells suspension calculate in the previous step into each of the macrowells that correspond to the grey color-coding in the plate map below.
    Fa21 M1D4 cell loading map.png
  6. Cover the top of your CometChip with plastic wrap then incubate in the 37 °C incubator in the main laboratory for 15 min.
  7. After the incubation, complete a wash step to remove excess cells that are not within the microwells of your CometChip. Read all the bullets below before proceeding!
    • Carefully remove the binder clips and the 96-well bottomless plate.
    • With the CometChip on the glass plate, 'waterfall' ~5 mL of 1x PBS over the wells.
      • Hold the glass plate at a 45° angle over the dish that you used to store your CometChip.
      • Pipet up ~5 mL of 1x PBS.
      • Press the pipet tip onto the glass plate above your CometChip.
      • As you expel the 1x PBS, move the pipet tip from left-to-right.
      • The 1x PBS should pass over the top of the CometChip and fall into the dish.
    • Use a P200 tip attached to the pasteur pipet to aspirate the excess liquid from your CometChip wells.
      • Lightly touch the tip to the bottom of each imprinted well on the CometChip and immediately lift the tip from the agarose.
  8. Use the molten 1% low melting point (LMP) agarose is located in the 42 °C waterbath on the front laboratory bench to 'trap' the cells in your CometChip.
    • You will need to work quickly from this point as the LMP agarose will solidify as it cools.
  9. Using the P1000, pipet up 1000 μL of molten agarose from the bottle.
  10. Hold the pipet tip over the top left well of your CometChip and as you expel the agarose move the pipet tip from left to right. Ensure that each row of your CometChip gets covered.
    • The goal is to lightly cover the wells that contain cells, which will 'trap' the cells into the microwells.
    • If the LMP agar 'fell' off the CometChip in any areas during this process, it is important to 'fill in' those portions of the CometChip.
  11. Leave your CometChip undisturbed on the benchtop for 3 min then carefully move it to the 4 °C cooler for 5 min to ensure the LMP agarose solidifies.
  12. Use a microscope to ensure you have cells loaded into your CometChip (see image below).
Microscopy image of loaded CometChip. (A) Bottom of macrowell showing evenly spaced microwells. (B) Close-up of empty microwell. (C) Close-up of microwell loaded with cells.

In your laboratory notebook, complete the following:

  • Include the calculations completed to determine the volume of cell suspension added to each macrowell for the CometChip assay.
    • The cell suspension is 500K cells / mL and 25,000 cells were added into each well.
  • Given the number of cells that were loaded into each macrowell, estimate the number of cells per microwell.
    • Consider the likelihood that every cell you add to the well will fall into a microwell.
    • Perhaps calculate the surface area of the bottom of a well (of diameter 6.35 mm) and compare this to the size of the cells (~10 μm).
    • Also, remember that within each macrowell there are ~ 300 microwells, which are ~40 μm in diameter and 40 μm in depth.

Treat cells with H2O2

  1. While the LMP agar is solidifying at 4 °C, prepare the 20 μM treatment concentration of H2O2 in DPBS.
    • Be sure to prepare with DPBS as the diluent because the serum in media will inactivate H2O2.
    • For the H2O2 treatment conditions, As should also be included at the concentrations previously used for the exposure step.
  2. Retrieve your CometChip from the 4 °C and carefully attach a fresh bottomless 96-well plate to recreate the wells that you used for cell loading.
    • Secure the bottomless 96-well plate with binder clips as before.
  3. Add 50 μL of either DPBS or DPBS + 20 μM H2O2 to the appropriate wells according to the plate map below.
    Fa21 M1D4 H2O2 treatment map v2.png
  4. Carefully transport your CometChip to the 4 °C cooler and incubate for 20 min.
  5. Retrieve the CometChip from the cooler.
  6. Remove the bottomless 96-well plate and quickly rinse the CometChip.
  7. Immediately transfer the CometChip to alkaline lysis buffer to stop the cellular response.
  8. To ensure cell lysis is complete, incubate the CometChip macrowells in the 4 °C cooler for 24 hrs.

Electrophorese CometChip macrowells

Due to the timing of cell lysis, the Instructors will complete the below steps.

To ensure the steps required for preparing a CometChip are clear, the Instructor will provide a live demonstration of this process. The steps are detailed below so you can follow along!

  1. Remove your CometChip from the alkaline lysis buffer and wash in 1X PBS.
  2. Use a kimwipe to dry the GelBond side.
  3. Carefully move your CometChip to the gel electrophoresis station in the 4 °C cold room.
  4. Place your CometChip on the raised center region of an electrophoresis box.
    • Double-sided tape was applied to the gel electrophoresis box. Be sure you lay your CometChip on the tape strips and lightly press down with a pipet tip to ensure it is secure.
  5. Add enough of the alkaline electrophoresis buffer to the gel electrophoresis box to cover your CometChip.
  6. Leave the CometChip in the alkaline electrophoresis buffer (aka unwinding buffer) for 45 minutes.
  7. To separate the damaged DNA into 'comets', electrophorese for 40 min (at 16 V, or 1 V/cm).
    • It is important that the electrophoresis occur at 300 mA. To maintain the appropriate current, the volume of electrophoresis buffer may need to be adjusted. The teaching faculty will assist you in adding/removing electrophoresis buffer such that this value is reached.
  8. Carefully remove your CometChip from the electrophoresis box and place it in a dish.
  9. Obtain an aliquot of neutralization buffer from the front laboratory bench.
  10. Wash your CometChip by adding enough neutralization buffer to cover (~10-12 mL) and incubate for 5 min at room temperature.
    • Repeat this step for a total of 3 washes.
  11. Add the SYBR gold DNA stain to your CometChip and carefully move it to the 4 °C cooler.
    • Stain CometChip overnight.

Reagents list

  • agar, normal melting point (from Invitrogen)
  • GelBond film (from Lonza)
  • agar, low melting point (from Invitrogen)
  • phosphate buffered saline (PBS) (from VWR)
  • Dulbecco's phosphate buffered saline (DPBS) (from Sigma)
  • alkaline lysis solution: 2.5 M NaCl, 100 mM Na2EDTA, 10 mM Tris, 1% Trition-X
  • alkaline electrophoresis solution: 0.3 M NaOH, 1 mM Na2EDTA, pH 13.5 (from Sigma)
  • neutralization buffer: 0.4 M Tris, pH 7.5 (from Sigma)
  • SYBR gold DNA stain (from ThermoFisher)

Navigation links

Next day: Draft data slide for major assignment

Previous day: Use immunoflourescence staining to assess repair foci experiment