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ISSN: 2161-0444
Medicinal Chemistry
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Detection and Quantification of Protein Post-Translational Modifications Using Novel Microchannel Plate Autoradiographic Imagers

Wayne Grant Carter*

School of Graduate Entry Medicine & Health, University of Nottingham Medical School, Royal Derby Hospital Centre, Derby DE22 3DT, UK

*Corresponding Author:
Wayne Grant Carter
School of Graduate Entry Medicine & Health,
University of Nottingham Medical School
Royal Derby Hospital Centre Derby DE22 3DT, UK,
Tel: +44 (0)1332 724738
Fax: +44 (0)1332 724626
E-mail: [email protected]

Received date: November 17, 2012; Accepted date: November 23, 2012; Published November 26, 2012

Citation: Carter WG (2012) Detection and Quantification of Protein Post-Translational Modifications Using Novel Microchannel Plate Autoradiographic Imagers. Med chem S11:001. doi:10.4172/2161-0444.S11-001

Copyright: © 2012 Carter WG. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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Abstract

It is likely that all proteins are modified post-translationally, either enzymatically or non-enzymatically. Scientists have continued to develop suitable methodologies in order to study the ever burgeoning list of protein post-translational modifications (PTMs). For the study of PTMs, one must consider suitable assays by which the target protein can be detected, the site(s) of PTM determined, the stoichiometry and stability of the PTM evaluated, and the biological outcome of the modification assessed. Historically, one of the methods of choice for identifying which protein is modified, and the site and stoichiometry of modification, has been the utilisation of commercial radiochemicals. Of these, tritium (3H) has excellent potential to facilitate analyses of biochemical reactions, but has the weakest signal strength of the commonly employed biological β-emitters. Hence development of imaging devices that are superior to conventional film autoradiography will enable a better exploitation of the universal application of 3H for measuring PTMs. Herein, we discuss the current application of film autoradiography and the advantages of using microchannel plate (MCP) autoradiographic imagers.

Keywords

β-emitter; Microchannel plate; Post-translational modifications

Introduction

The most commonly employed laboratory radiochemicals for studying biological systems are β-emitters; including tritium (3H), 14C, 35S, 33P, and 32P. These β-emitters differ in their energetic strength, with 3H being the weakest β-emitter, rising to 32P, the strongest (Table 1). By using a β-emitter of relatively high strength there will likely be a corresponding reduction in autoradiographic exposure time. However, the relatively stronger (more penetrative) β-emission from 32P is potentially hazardous to the experimenter, and therefore laboratory work is confined to behind 1 cm of perspex shielding. Radioactivity safety practices are still required for 3H use, but user-shielding is not required. For laboratory studies, one will also need to consider the timeframe of experimentation: 32P has a half-life of 14.3 days, so optimal radiolabel usage is restricted. By comparison 3H has a half-life of 12.4 years, so although both of these radiochemicals may be susceptible to hydrolysis and decomposition, there is much less restriction on laboratory shelf-life with 3H. Additionally, although 32P has proved an invaluable asset for the study of phosphate transfer in the dynamic activity of kinases and phosphatases, it has less universal application to the study of other biomolecules. By contrast, organic molecules that contain a hydrogen atom may in theory be labeled to form a tritiated derivative. Thus 3H can be more extensively utilized in biomolecular studies than 32P.

β-emitter Signal strength Maximal energy (MeV)
3H Weak 0.019
14C Weak 0.156
35S Weak 0.167
33P Medium 0.249
32P Strong 1.709

Table 1: Commonly employed laboratory β-emitters.

Methodology

One major drawback of 3H use is that its weak signal strength may require signal amplification for detection. The weak β-emitter energy of 3H can be harnessed as photons in liquid scintillation counting (LSC), or fluorometric autoradiography. To determine which protein is modified within a protein mixture, protein resolution by sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) is commonly employed, but direct 3H escape for autoradiography is limited. Several steps can be undertaken to improve the weak emission of 3H β-emitters to provide suitable autoradiography. After 3H-radiolabelled protein resolution by SDS-PAGE, the gel can be impregnated with a fluorophore, such as sodium salicylate and then the gel dryed. To improve linearity and sensitivity of a film signal, the film may also be preflashed and then autoradiography performed at a low temperature, typically -80°C. However, even with these additional measures to facilitate 3H signal acquisition, exposure times of days to weeks may still be required to provide sufficient cumulative autoradiographic signal [1].

Contrary to these additional manipulations, the relatively strong β-emitter 32P may only require short-term and direct auto radiographic exposure. Direct autoradiography of 32P will afford sensitivity and resolution, but signal capture may also be enhanced using intensifying screens, although this will reduce signal resolution. By either direct autoradiography or from the use of intensifying screens, the superior signal strength of 32P facilitates typical film autoradiography exposures of only hours to days, and as with 3H, this is usually accomplished from autoradiography at low temperatures (-80°C). These major differences in the properties of 3H and 32P are summarized in Table 2. Hence, ultimately an improvement in the sensitivity of 3H autoradiography will facilitate the broader exploitation of 3H as a radiolabel used for the study of biological systems [1].

β-emitter Relative Signal
strength
Half-life Signal Containment Biological analyses Signal
amplification
Film autoradiography
3H 1 12.4 years Bench work & monitoring Organic molecules. PTMs e.g.
alkylation, methylation
Fluorometry Days-weeks
32P 90 14.3 days User shielding behind 1 cm of perspex Phosphate transfer. PTM as phosphorylation Intensifying screens Hours-days

Table 2: Comparison of the physical properties and biological application of 3H and 32P.

The current commercial market availability of instruments for sensitive 3H imaging is not extensive. Commercial phosphor-imagers with plates suitable for 3H are available, and alternatively, microchannel plates can provide the proximity sensor for 3H β-particles. Microchannel plate (MCP) autoradiographic imaging was developed independently at a number of sites, including the University of Leicester Space Research Centre [2-4]. In contrast to film autoradiography, MCP imagers have a lower radiolabel signal threshold (higher sensitivity) of 6 dpm/ mm2, and are able to detect radiolabel signal linearly over six orders of signal magnitude. Additionally, MCP radiolabel signal detection is in real-time, with an on-screen display, and this is operational at room temperature. Other useful properties of MCP imagers include low intrinsic background noise of 5×10-6 counts/sec per autoradiographic signal (pixel measurements), a spatial resolution of ~70 μM, and an imaging window of 9.3 cm × 9.3 cm; suitable for 1D and 2D PAGE mini-gel visualisations, or the analysis of several standard microscopy slides in a single autoradiograph. Finally, the MCP imager has internal software which allows direct quantitation of pixel measurements without the need for further densitometric analysis.

Results and Discussion

The superior sensitivity and reduced exposure time of MCP imagers has enabled us to track protein post-translational modifications (PTMs) that would normally be difficult to detect, as they lie at or below the sensitivity threshold provided by conventional film autoradiography. For example, we have studied PTM (adduction) of proteins by commonly encountered commercial organophosphorus (OP) pesticides. Undesired exposure to environmental pesticides is a global health concern. The toxic effects of acute, substantive exposure may usually be attributed to frank cholinergic poisoning as a consequence of adduction to and inhibition of acetylcholinesterase (AChE) within nerve synapses. However, inadvertent protein adduction (covalent binding) or direct binding to other secondary proteins remains a health concern, and moreover, cumulative low-level exposure may result in ill-health without triggering detectable signs of cholinergic inhibition [1,5-7].

To track OP pesticide adduction of proteins in vitro, one would use individual radiolabelled pesticides, but they are not available commercially. A commercial OP, 3H-diisopropylfluorophosphonate (3H-DFP) can be purchased, and we utilized this broad-binding OP to track pesticide adduction targets. Our strategy to detect pesticide PTM of proteins, under conditions of relatively low levels of AChE inhibition was to either dose animals with pesticide in vivo or preincubate animal tissue in vitro with pesticide, and then radiolabel any free OP adduction sites using 3H-DFP. Adduction of a protein target by a pesticide resulted in a reduction in subsequent 3H-DFP radiolabelling and this was quantified using MCP autoradiographic imaging. The imaging window of 9.3 cm×9.3 cm allowed us to autoradiograph 3H-DFP proteins that had been resolved by either 1D or 2D mini-gel PAGE.

The level of pesticide adduction (fall in 3H-DFP radiolabelling) was quantified in protein bands using the intrinsic MCP β-acquisition software. This software provides a direct quantitation of the pixel density (radiolabelling) across the length of a gel lane. Hence a direct comparison (and quantitation) of radiolabelling at each 3H-DFP protein band can be made between controls and test pesticide preincubations [1,5-7].

There is the potential to utilize this preincubation strategy to enable detection of other PTMs, but if radiolabels are available to monitor the PTMs directly this may not be required. As an example of this, we have followed PTM as carboxyl methylation, and after 2D-PAGE of radiolabelled methylation targets, we were able to identify novel targets of protein PTM [8]. If the targets of PTM lay below the threshold of protein visualization methods such as Coomassie or silver staining (~0.1 ng) then column chromatography may facilitate protein enrichment, with MCP autoradiography utilized to track the proteins of interest [1,5-7].

Finally, the imaging window is also of suitable size to enable simultaneous autoradiography of 3 glass microscopy slides. For a standard microscopy slide (75 mm×25 mm) we typically apply 3 tissue sections; hence 9 simultaneous images can be acquired in a single autoradiograph. We have utilized this rapid and sensitive imaging to examine brain microlocalisation of radiolabelled ligands in the mice brain [7]. From H & E staining of brain tissue sections visual landmarks provided an anatomical guide onto which the autoradiogram was superimposed to enable radiolabel localization [7].

In summary, 3H has excellent potential for the study of PTMs of biological molecules, but there is a need for sufficiently sensitive equipment, such as MCP digital autoradiographic imagers to match and respond to the study of an ever expanding list of protein PTMs.

Acknowledgements

The author would like to thank the Medical Research Council and Syngenta for financial support for some of the research studies described in this manuscript.

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