Bioluminescence refers to the ability of living things to produce light and represents a fascinating and profoundly useful area of biophotonic research. Not only is it of interest to study and record the bioluminescent emission of organisms in their natural environment (~ 90% of deep sea marine life exhibits bioluminescence), but several of the individual biomolecules that give rise to bioluminescence have been identified, isolated, studied, often genetically coded, and put to use across a range of applications. These uses have penetrated a broad field of study, including intracellular physiology, pre-clinical research, microtitre and biochip-based assays, and even art!A well-known bioluminescence, and one that has been ubiquitously harnessed for research purposes, is that induced by the luciferase enzyme. For example, firefly luciferase emits light in the presence of its substrate luciferin & Adenosine TriPhosphate (ATP) and is widely used for measuring ATP concentrations. Since all living organisms contain ATP it finds principle use as a measure of bio-contamination, for example in the food industry. Importantly, luciferase has been coded and adopted as a gene reporter, routinely transfected into living organisms and cells to study, for example, expression levels and cell physiology.
Serial dilution of luminescent biomarker HRP in illuminol/peroxide showing effect of increasing EM gain factors from x1 to x500. At x1 gain setting the lower concentration wells on the right hand side of the microtiter plate are indistinguishable from the noise.By increasing the gain of the EMCCD, these wells become clearly visible above the noise floor.
BRET can offer some attractive advantages over Fluorescence Resonance Energy Transfer (FRET) based assays. An example of BRET might use a bioluminescent luciferase that is genetically fused to one candidate protein, and a Green Fluorescent Protein (GFP) (or mutant of) fused to another protein. When the two proteins bind, the luciferase excites luciferin, which transfers its excited state energy to GFP causing it to emit efficiently in the green. GFP-Aequorin is a conjugate often used for Ca2+signalling. In the jellyfish Aequorea Victoria, the chemiluminescent Ca2+ binding protein aequorin is associated with GFP. Upon binding to Ca2+, this calcium-activated protein converts the chemical energy stored in coelenterazine into an oxidized form of coelenterazine. If GFP were not present, oxidized coelenterazine would emit blue light but with low quantum yield. However when GFP is nearby (as it is in vivo), excited state energy is instead transferred to GFP, which then emits more efficiently in the green. A calcium-sensitive reporter gene has been constructed coding for aequorin fused to GFP. Such a bioluminescent genetic marker can have the advantage over Ca2+ - specific fluorescent dyes of being easily targeted to specific cells and sub-cellular compartments. With the negligible background, sub-second exposure times can be enough to record the signal in single cells expressing any of the fusion proteins, especially when using Electron Multiplying CCD (EMCCD) technology to detect.
Production of visible light by a chemical reaction is called chemiluminescence (in fact, when a reaction of this nature occurs in living organisms, it is called bioluminescence). Chemiluminescence occurs when an energetic (exothermic) reaction produces a molecule in an electronically excited state. That molecule, as it returns to the ground state, releases its energy as a photon of light. The rate of production of light and concentration of chemiluminescent molecule, often coupled to concentration also of a catalytic reagent, imposes limits on the amount of time that this luminescence can be usefully observed from a sample volume. Some samples will generate a relatively bright signal for a short period of time (until all of the chemiluminescent reagent is used up), others will yield a weaker signal over a longer period. For the latter it can be more important to use a deep cooled CCD, capable of accumulating over a long period without significant darkcurrent build-up.
As mentioned previously, luminescence can be utilized in a variety of common imaging formats and techniques:
Common to all of these approaches is the fundamental need for both a sensitive CCD detector and a light-tight imaging environment, the latter often provided by an imaging dark box (even to house a microscope).
With bioluminescence and chemiluminescence, light is emitted directly by the specimen without the need to put in excitation light first of all. In terms of signal to background, this carries a key advantage in that there are no sources of undesirable autofluorescence background emission or scatter. Photobleaching and phototoxic effects (in living cell studies) are also markedly minimized. The lack of autofluorescent background in turn puts the emphasis very much on the CCD detector to operate with minimal sources of detector noise, since it is the CCD noise floor that is most likely to represent the true detection limit (as opposed to background photon noise). This means that:1. Read noise has to minimized relative to the amount of photons collected over a given exposure time.2. Darkcurrent must also be fundamentally low, especially if long exposures are used and/or if EMCCD technology is being utilized. Furthermore, since luminescence is typically a relatively weak phenomenon, a high Quantum Efficiency (QE) is desirable in order to generate a high signal-to-noise (S/N) within a relatively short exposure time, assisting both dynamic intracellular processes and/or sample throughput.
There are several back illuminated Andor CCD formats suited to ultrasensitive imaging of bio/chemiluminescence, depending on the type of experiments you are conducting. Figure 2 shows a QE curve representative of Andor's recommended back illuminated CCD and EMCCD cameras for luminescence.
Quantum Efficiency and Fluorescent Dyes relevant to Bioluminescent & Chemiluminescent Imaging.
iXonEM+ EMCCD Camera
Features & Benefits of the iXonEM+
Bioluminescence images taken with iXon DV887 front-illuminated: (a) and (b) Plan view and surface intensity plot (respectively) of an agar plate streaked with an Escherichia Coli strain containing bioluminescence genes; (c) Surfaceintensity plot showing bioluminescence output at the leading edge of a motile bioluminescent bacterial strain. The bacterial strain was point inoculated at the centre of a low concentration agar plate and allowed to swim radially outward. Courtesy of Dr Mike Winson, Institute of Biological Sciences, University of Aberystwyth, UK
iKon-L CCD Camera
Features & Benefits of the iKon-L
Features & Benifits of the iKon-M
Representative spots from an optimized biochip array recorded with an iXon DV865 EMCCD camera demonstrating the effect of EM gain for detecting extremely weak levels of gene expression.
The choice whether or not to opt for EMCCD for bio/chemiluminescence depends very much on your ability to employ longer exposure times to collect enough signal. The rule of thumb is that if long exposures can routinely be employed, such that enough photons can be collected to significantly overcome the read noise floor, then a low-noise, deep-cooled, back-illuminated iKon slow-scan camera platform is recommended. In some experiments, as in some assays, the decision to adopt long exposures can come about through the desire to exceed a certain Signal to Shot Noise threshold, which in turn is linked to the Coefficient of Variation (CV) of the assay. In such scenarios, there can be no alternative but to simply collect enough photons in order to reach this S/N level, which may be well above the noise floor of a deep-cooled, slow-scan iKon camera. At these signal levels, EMCCD (i.e. the ability to render the read noise floor negligible) may make little difference to the overall S/N.
On the other hand, if it is deemed that if either kinetic measurements (such as monitoring of intracellular calcium flux using aequorin-GFP) or sample throughput is more important, then one wants to limit the exposure time accordingly. Under such circumstances, the read noise floor of the detector may become significant with respect to the signal intensity, and EMCCD should be considered to improve the overall S/N. Finally, it should be remembered that EMCCDs can essentially be made single photon sensitive, and can even be used to count individual bio/chemiluminescent photons!
Courtesy of Dr Mike Hepher, School of Built and Natural Environment, Glasgow Caledonian University, UK
Description of Dr Hepher's images:Selected images from rapid kinetic series, recorded with the iXon DV860 camera (30ms exposure). It shows a sono-chemiluminescence effect where light is emitted form an ultrasonic reaction chamber containing a solution of luminol. During sonocation of an acqueous fluid, OH radicals are produced from the breakdown of water molecules. The luminol glows as it reacts with OH radicals. The camera sensitivilty is such that no peroxide is required for the reaction to proceed, even at short exposure times.Top - a cross section of the sound field and the maximum areas of emitted light in the reactor.Side - a reactor being optimized for maximum OH radical production. Initially, the starting fluid level shows no luminescence activity. As fluid level is increased, conditions for OH radical production improve during the kinetic series, indicating constructive interference of sound waves.
HeLa cells transiently-transfected with NFkB-luciferase were stimulated with TNFa and imaged for 16 hours. Exposure time per frame was 5 minutes using 1MHz conventional mode readout of the Andor iXonEMDV887 back-illuminated. Images courtesy of Prof Mike White, Centre for Cell Imaging, University of Liverpool, UK.
Please call an Andor sales representative or application specialist for further advice as to the ideal camera choice for your experiment(s).
Schematic overview of Andor iQ - showing the core and interfaces to Windows hardware and software components.iQ hosts provide API’s (shown in light blue) to support 3rdparty hardware and software extensions. The interface to Windows API is at many levels, but pre-emptive swapping is encapsulated in the M-DMM.
Features & Benefits of Andor iQ
Features & Benefits of Solis(i)
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