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Angled Dispenser Tips for Reagent Addition to Live CellsDownload
Related Products: Cytation 1, Synergy H1, Synergy Neo2
June 16, 2014
Live cell-based assays have become ever more popular in microplates. While calcium flux assays have been the hallmark of G-protein coupled receptor assays for quite some time, recently high content phenotypic analysis of live cells is being used in drug discovery. As with homogeneous assays, a subset of cell-based assays requires the use of reagent dispensers that have been integrated into the microplate reader. There are numerous reasons to use automated reader dispensers in conjunction with a cell-based microplate read.
The rapidity of response in some kinetic assays requires precise timing between the addition of a critical reagent and the determination of the results. Only with appropriate reader control of the reagent addition can the timing be evaluated at a high enough tolerance to insure that all wells are treated the same. For example, calcium flux reactions often take place over the course of a several seconds, which would preclude the addition of reagents manually.
Convenience is another reason to use automated reagent dispensers. The addition of reagent periodically over long time periods, laborious if added manually, can be automated with integrated reagent dispensers. This saves time and energy, while providing more consistent results.
Many microplate readers have temperature and CO2 and/or O2 gas control, and removing the plate from the reader would expose the cells to ambient temperature and atmospheric gas concentrations. The use of integrated dispensers can also avoid the exposure of the cells to environmental changes such as temperature or gas concentrations. Figure 1.
Figure 1. Schematic Depiction of Fluid Flow with Straight Dispenser Tips. Straight tips provide the best reagent mixing at the expense of potentially displacing adhered cells.
To get the most consistent results when using reagent dispensers, it is critical to rapidly mix the added reagent to the existing liquids within the microplate well. Volume, rate, and tip position are three important parameters in regard to mixing. The volume of reagent being dispensed relative to the amount of fluid already in the well is probably the most influential parameter. More efficient mixing will occur when a greater percentage of reagents being added to the total volume (existing + fluid added). For example adding 100 μL of (3 mM) solution to an existing 200 μL will mix more efficiently than if 5 μL of a 60 mM solution was added to 295 μL, even when the final concentration of reagent is the same (1 mM). Not surprisingly the rate at which fluid is added can also affect the mixing efficiency, with faster fluid rates being more effective at mixing than slower rates. Reagent tip positioning can also play a role. The fluid entry angle into the well and the tip position relative to the well-center are both important parameters. Centering the dispense tip on the well and vertically oriented provides the best mixing profile.
Unfortunately, the high efficiency mixing provided by straight tips can be deleterious for cell-based assays. The force and volume of fluid being injected into the well may be sufficient to displace cells adhered to tissue culture-treated microplates. This is of particular concern for microscopy applications as the cells will no longer reside in the focal plane and will thus not be imaged. A good example of this phenomenon is demonstrated in Figure 2, where NIH3T3 fibroblast monolayer was significantly impacted by a reagent dispense.
Figure 2. Affect of Straight Dispenser Tip Design on Cell Monolayer. GFP expressing NIH3T3 cell monolayers in 384-well plates were subjected to a fluid dispense (25 μL PBS) using a straight dispense tips. Wells were imaged at 4X before and after dispense using a Cytation 3.
In this example the force of the dispensed fluid flow was enough to overcome the dampening affects of the fluid already present in the well and scour away the cells from the microplate bottom, much like a fast flowing stream will move rocks on a streambed. The liquid already present in the well normally serves as a buffer to slow the dispense fluid, but too little well fluid or too much reagent can overcome the shock absorbing capacity of the well. While one might be able to alter the volume or dispense-rate of fluid being added to avoid monolayer damage, the easiest solution is to use angled tips with live cell based assays that require reagent addition within the reader.
By directing the flow sideways, fluid is no longer directed straight downward towards the cell monolayer, but rather through the fluid on top (Figure 3). This provides efficient reagent mixing without displacing adhered cells.
Figure 3. Schematic Depiction of Fluid Flow with Angled Dispenser Tips. Angled tips allow the dispensing of fluid against the side of the well dissipating some of the fluid force and allowing cells to remain adhered.
BioTek has developed a new dispenser tip option for the Synergy H1, Synergy Neo and the Cytation 3 to dispense reagents to live cells (Figure 4). The standard dispenser head uses stainless steel tubing fitted into an assembly allowing for easy “tool free” installation and removal from the reader. The new optional dispenser head (P/N 1320514) uses stainless tubes that have been angled 20° in the same quick change assembly. In addition, the dispenser head is offset such that the ends of the angled tips are positioned at the same spot above the well as the standard dispenser head tips. This feature enables the end user to use either dispense head interchangeably without having to worry about positioning or changing plate data files.
Figure 4. Angled tip design. Dispenser tips with a 20° angle allow fluid dispense without displacing adhered cells. Changeable design allows switching between angled and straight tips, which work best with homogeneous assays.
Figure 5. Affect of Angled Dispenser Tip Design on Cell Monolayer. GFP expressing NIH3T3 cell monolayers in 384-well plates were subjected to a fluid dispense (25 μL PBS) using 20° angled dispense tips. Wells were imaged at 4X before and after dispense using a Cytation 3.
The effectiveness of the new design is demonstrated in Figure 5. NIH3T3 cells expressing GFP where grown to confluency in 384-well plates and subjected to a 25 μL fluid dispense. Representative images taken of the same well before and after reagent addition show virtually no damage to the cell monolayer. An example of the utility of the angled dispenser tips is their use in monitoring calcium flux with GPCR activation. CHO cells loaded with FluoForté dye (Enzo Biochem) demonstrate a rapid increase in fluorescence due to calcium flux upon stimulation with histamine (Figure 6). Ligand induced G-protein coupled receptor (GPCR) activation is known to result in increased intracellular calcium ion levels. As free calcium ion levels increase their interaction with the calcium sensitive dye results in fluorescence intensity increases. The rapidity of the calcium change requires that the reader dispenser tips be use to add the stimuli.
Figure 6. GPCR activation induced Calcium Flux. 20x images of CHO cells loaded with FluoForté before and after stimulation with 1 μM histamine and the fluorescence imaged. Time in seconds after stimulation is indicated in each image.
As stated previously, not all assays are the same when it comes to reagent addition. There are always compromises in regards to reagent volume, concentration, and dispense rate with optimization. With homogeneous assays, the key element is typically adequate mixing without spilling or overflow of liquids inside the reader. Live cell-based assays have an added layer of complexity in that the adhered cells need to be maintained within the context of adequate fluid mixing. The angled dispense tip is another tool that can be used for assay optimization.