Team:Dundee/Forensic Toolkit/FluID
Blood
Click here to jump to our blood lab report where we purify the human proteins haptoglobin and haemoglobin B
Semen
In order to gain a deeper insight into the field of forensics, we liaised with a diverse mix of professionals, from criminal lawyers to crime writers, who kindly shared with us their advice and expertise.
Blood
Introduction
There is a lot of potential information contained in a blood stain, which is why forensic investigators are so keen to seek it out. Most importantly, DNA can be extracted from blood samples and can be linked to a suspect or can eliminate a suspect from suspicion. The blood spatter pattern can reveal information about the type of weapon used and the position of the victim and culprit for example. Finally, blood typing can be used as an initial test to exclude some suspects however, blood type alone is not enough to identify a suspect because lots of people will also share the same blood type.
There are currently several different methods for detecting blood at a crime scene, each with its own advantages and disadvantages. The main methods used are Luminol or ALS (alternate light source) ‘crime-lite’. These crime-lite’s are essentially a box of different coloured torches. Different biological fluids will absorb light at different wavelengths and are thus more visible to the naked eye using this technique. However, a positive reaction using this technique is not really confirmation for the presence of body fluid since other substrates may also fluoresce. It can also be a very slow process at the crime scene, with different crime lights, being used one at a time on all surfaces to try and identify any body fluid present.
Luminol (which you might have seen on TV programmes such as CSI) is a compound used to detect blood at a crime scene. The investigator prepares a solution of luminol and sprays it on the area under investigation. The lights are then turned off and any traces of blood show up as a bright blue glow. This is because the luminol reacts with iron in blood to produce chemiluminescence (which is the emission of light during a chemical reaction). The main advantage of Luminol is that it glows in the presence of very small quantities of iron so even trace amounts of blood can be detected. However, the disadvantages of this technique are that the chemiluminescence can also be triggered by a number of substances such as copper and bleach. This means that if a crime scene has been cleaned with bleach, the bleach residue will cause the entire crime scene to glow blue and this camouflages any traces of blood that might be present. In addition, the reaction tends to be very fast, only around 30 seconds before it stops glowing. Our spray will hopefully fluoresce for much longer, giving plenty of time for the scene to be analysed and photographed without the need for constant reapplication of the spray.
For the blood detection we have decided to exploit the interaction between haptoglobin and haemoglobin.
Figure 1 - Structure of the human haptoglobin-haemoglobin complex.
Haemoglobin is the tetrameric protein molecule in red blood cells that carries oxygen. It is composed of four polypeptide chains, which in adults consist of two alpha (a) globin chains and two beta (b) globin chains. In blood plasma, haptoglobin binds free haemoglobin released from red blood cells, inhibiting its oxidative activity. The haptoglobin-haemoglobin complex can then be removed by the reticuloendothelial system which is a part of the immune system. Despite this, haemoglobin is still found free in the blood plasma at a concentration of up to 0.1g/l and this is what we hope to detect.
In order to detect blood using FluID, haptoglobin will be attached to carboxylate-modified fluorescent microspheres and in theory when our FluID is applied to a blood sample the haptoglobin will bind haemoglobin and allow for easy visual detection of the fluorescence given off. Our aim was to overexpress this protein in E. coli, purify it and attach it to carboxylate-modfied fluorescence micorspheres.
Results
The first step of this process was optimising the genes encoding human haptoglobin and the haemoglobin alpha and beta subunits for E. coli and modifying them to ensure they were compatible with BioBrick specifications and standards. These genes were then ordered from IDT (Integrated DNA Technologies) and cloned into pSB1C3 to give the following BioBricks; BBa_K1590000, BBa_K1590001, and BBa_K1590002. These were then sub-cloned into the pQE80-L vector which allows for inducible expression of our target proteins along with an N-terminal polyhistidine-tag. Using the pQE80-L we aimed to overexpress each component and attempted to purify them using nickel affinity chromatography.
To characterise the interaction between haptoglobin and haemoglobin we wanted to use both in vivo and in vitro techniques. To do this, the idea was to carry out crosslinking experiments as well as a bacterial two hybrid screen with haptoglobin and haemoglobin alpha or haemoglobin beta. Crosslinking is the process of chemically joining two or more molecules by a covalent bond. This attachment between groups on two different proteins results in intermolecular crosslinks that allow a protein-protein interaction to be stabilised, captured, and analysed using a western blot.
The bacterial two hybrid screen, based off of the original yeast two hybrid system which uses a reconstituted transcription factor, uses enzymatic activities to detect physical interactions between proteins. You can read more about the theory behind the bacterial two hybrid system, linked below.
We have successfully purified both haptoglobin and haemoglobin beta using a polyhistidine-tag and nickel affinity purification. In the case of haemoglobin beta this was followed up with size exclusion chromatography to further purify our protein. Unfortunately haemoglobin alpha subunit proved more difficult to overexpress.
Overexpression and Purification of Haemoglobin Beta
Overexpression of haemoglobin beta.
We subcultured 50µl of an overnight culture into fresh LB containing the appropriate antibiotics (ampicillin and kanamycin) and grew the cells at 37°C until an OD600 of ~0.6 was reached. The expression of protein was then induced by adding 1mM of IPTG then the cells were grown for a further 3 hours at 37°C. 1ml of this culture was then taken for analysis by western blot which showed that haemoglobin beta was successfully overexpressed. The results from this are illustrated below in figure 2.
Figure 1 - Overexpression of haemoglobin beta. Single colonies of M15[pREP4] E. coli containing pQE80-L encoding hHBB were used to inoculate 5ml of fresh LB growth medium supplemented with ampicillin and kanamycin. These overnight cultures were then subcultured and grown at 37°C. Once cultures reached an OD600 of 0.6, they were induced with a range of IPTG concentrations. They were left to grow for a further three hours at 37°C, after which 1ml aliquots were pelleted, re-suspended in 100µl of Laemmli buffer and 20µl of these samples were separated by SDS-PAGE (12% acrylamide). This was transferred to a nitrocellulose membrane and probed with an anti-his antibody.
Purification of haemoglobin beta.
This was then scaled up and 4 litres of E. coli containing pQE80-L hHBB was grown for purification of haemoglobin beta by nickel affinity FPLC (fast liquid chromatography). The optimum conditions for this were as follows: 4 x 1L of fresh LB growth medium containing ampicillin and kanamycin was inoculated with 50ml of haemoglobin beta overnight culture and left to grow until an OD600 of between 0.6-1 at 37°C. The expression of protein was then induced by adding 1mM of IPTG then the cells were grown for a further 6 hours at 20°C. Using FPLC, the supernatant was loaded onto a nickel column and the protein was eluted using an increasing concentration of imidazole. The results from this can be seen in figure 3.
Figure 3 - Purification of haemoglobin beta by nickel affinity FPLC (fast protein liquid chromatography). Our sample was loaded onto a nickel column and the protein was eluted. This peak corresponds to haemoglobin beta and the corresponding fractions were collected for further analysis by SDS-age, western blotting and SEC.
The fractions corresponding to the peak were retained and concentrated down to 500μl for further purification by size exclusion chromatography (SEC). You can see the results from the SEC purification and further characterisation below in figure 4.
Figure 4 - Characterisation of haemoglobin beta following SEC (size exclusion chromatography). A) The sample of concentrated fractions containing haemoglobin beta from nickel affinity purification was loaded onto an SEC column and the protein was eluted. B) 10µl of each fraction corresponding to the two observed peaks was mixed with 10µl of laemmli buffer and loaded onto an SDS gel. The bands observable on the gel are in line with the expected size of haemoglobin beta - 16kDa. C) Western Blotting was then carried out against an anti-his antibody to confirm the presence of haemoglobin beta.
Overexpression and purification of Human Haptoglobin
Purification of haptoglobin
Like haemoglobin beta, haptoglobin was overexpressed and purified by nickel affinity FPLC. The fractions corresponding to the peak observed on the chromatogram (not shown) were ran on an SDS gel shown below in figure 5.
Figure 5 - Purification of human haptoglobin by nickel affinity FPLC (fast protein liquid chromatography). Our sample was loaded onto a nickel column and the protein was eluted. The fractions corresponding to a peak were collected. A) 10µl of each fraction was mixed with 10µl of laemmli buffer and loaded onto an SDS gel. The bold bands observable in fractions A9-A11 are in line with the expected size of haptoglobin - ~45kDa. B) Samples separated by SDS-PAGE were transferred to a nitrocellulose membrane and probed with an anti-his antibody to confirm the presence of haptoglobin.
The fractions obtained from nickel affinity chromatography were concentrated down to 500 µl and loaded onto the Superdex 75 10/300 to carry out size exclusion chromatography. Results from this can be seen in figure 6.
Figure 6 - Further characterization of human haptoglobin following SEC. A) Chromatogram showing the purification profile of the His-tagged human haptoglobin. The fractions corresponding to the two peaks observed on the chromatograph were further analysed by SDS page gel and western blotted. B) 10µl of the fractions A8-A9 and A9-A10 corresponding to peaks 1 + 2, respectively were mixed with 10µl of laemmli buffer and loaded onto a 12.5% SDS-PAGE gel. Band A observed on the gel corresponds to the expected size of haptoglobin – 45kDa. However, it is not clear what the bands present at ~37kDa may be. C) Samples separated by SDS-PAGE were transferred to a nitrocellulose membrane and probed with an anti-his antibody. This Western blot analysis confirmed the presence of human haptoglobin.
To further identify the expressed protein at ~45kDa, the band was cut and sent off for analysis by mass spectrometry. This technique uses the proteolytic enzyme trypsin which cleaves at the carbolic side of arginine and lysing residues. The sizes of the peptide fragments obtained after trypsin digestion, represent the peptide mass fingerprint and are characteristic of each protein. The peptide mass fingerprint spectrum of fragments derived through trypsin digest indicated that haptoglobin was indeed purified with good coverage of the amino acid sequence to the expected sequence (figure 7). This shows that we have purified two forms of our protein, once containing the histidine tag and the other which has lost the tag. An attempt will be made to attach both of these to the fluorescence micorspheres.
Figure 7 - Mass spectrometry analysis of haptoglobin.The expected sequence of haptoglobin is shown here with the matched peptides from the mass spectrometry analysis shown in bold red.
Conclusion and Future Work
Further work is needed to optimize the conditions for the expression of haemoglobin A. This has proved difficult and has been one of the biggest challenges in the lab for the blood detector aspect of FluID. To do this we could alter growth conditions such as temperature to decrease the rate of protein synthesis and hopefully lead to a more soluble protein being expressed. We could also alter the concentration of IPTG added to induce protein over expression or add sucrose to help stabilize the protein structure, this works by increasing the osmotic pressure within the E. coli cells leading to the expression of osmoprotectants which stabilise native proteins.
We would also hope to thoroughly test the interaction of haptoglobin with haemoglobin both in vivo and in vivo as well as both attached to and separate from a flourosphere to see whether fusion of haptoglobin to a fluorescent particle might alter the protein-protein interaction in any way. This would involve competing our crosslinking experiments of haptoglobin to haemoglobin alpha and beta using two different fixing agents - DSS (disuccinimidyl suberate) and formaldehyde.
DSS reacts with primary amines which are generally found on lysine side chains and the N-terminal of the peptide chain to form amide bonds. While, formaldehyde, a classic fixative, also reacts with primary amines to form Schiff bases, and with amides to form hydroxymethyl compounds which can condense with another amide moiety to form methyl diamides.
To fully test the interaction in vivo our bacterial two hybrid screen would need to be completed. So far we have managed to test haemoglobin alpha with haemoglobin beta together and haptoglobin together with haemoglobin alpha. However, this has only been carried out in one configuration meaning we would need to repeat these experiments with our proteins fused to the opposite T18 or T25 fragment. Because the plasmids encoding these fragments have different copy numbers, the results from our assay could be affected by this. Steric hindrance may also occur in only one configuration so both need to be tested to avoid a false negative result due to this. We would also need to test haptoglobin against haemoglobin alpha to complete the bacterial two hybrid screen.
Finally, it would be great to be able to test our devices sensitivity. To do this our haptoglobin fused flourospheres would need to be let loose on real blood samples of different concentrations and the binding affinity measured.
↑Semen
Introduction
For semen detection our main target ligand is the polyamine spermidine which is found in relatively high concentrations in seminal fluid (5-15 mM). Spermidine is made from another polyamine called putrescine and is the precursor of spermine. Regulation of polyamine synthesis, degradation and transport is tightly controlled in bacteria. In E. coli, two of three identified transport systems are ABC transporters composed of a periplasmic binding protein, a pair of transmembrane proteins and a membrane protein possessing ATPase catalytic activity. Out of these three components, we were interested in investigating the periplasmic binding protein PotD which specifically binds spermidine. The fact that this protein is responsible for transportation of spermidine and lacking in enzymatic activity meant that it was an ideal candidate for use in FluID for semen detection.
Figure 1 - Crystal structure of PotD in complex with its ligand spermidine. PotD (blue) is a binding protein specific to spermidine (red) which is a polyamine found in semen.
As with the other binding proteins, our aim was to overexpress this protein in E. coli, purify it and attach to it carboxylate-modified fluorescent microspheres.
Results
The gene encoding PotD was amplified from E. coli MG1655 and cloned into both the biobrick vector (BBa_K1590009) pSB1C3 and the high expression vector pQE80-L. The pQE80-L vector allows for inducible expression of our target proteins along with an N-terminal poly histidine tag.
Figure 2 -
Characterisation of PotD. Single colonies of MC1061 E. coli containing pQE80-L encoding PotD were used to inoculate 5ml of fresh LB growth medium supplemented with ampicillin. Once cultures reached an OD600 of 0.6, one was induced with 1mM IPTG and one was left uninduced as a control. They were left to grow for a further three hours, after which a 1ml sample was taken and the cells pelleted. The cells were resuspended in 100µl of Laemmli buffer, 20µl of which was separated by SDS-PAGE and transferred to a nitrocellulose membrane and probed with an anti-His antibody.
Upon successful expression of PotD-His 3 L cultures were grown up for protein purification purposes, under the same conditions. However, instead of allowing a further 3 hours growth after induction, the cultures were left for 12 hours at 37°C. This was to ensure that plenty of protein was being produced and since PotD is native to E. coli, leaving them to grow this long did not have a significantly detrimental impact upon the cells. We used His tag affinity and size exclusion chromatography to purify PotD. The fractions taken from affinity purification were concentrated to a volume of 500 µl and further purified using SEC.
Figure 3 - Characterization of PotD. A) Chromatogram showing the purification profile of the his-tagged human HBN protein. The fractions corresponding to the two peaks observed on the chromatograph were further analysed on SDS page gel. B) Coomassie Stain of the purified fractions (A12 + B12). 10 µl of each fraction was mixed with 10 µl of 2x Laemmli buffer and loaded onto an SDS gel which was ran for 1 hour at 100V and then stained. These were then western blotted to confirm the presence of our target protein PotD-His.
Figure 4 - Samples from the SEC were ran on a 12.5% SDS-PAGE gel and then transferred to a nitrocellulose membrane and probed with an anti-His antibody. The band detected in the blot corresponds to the expected size of PotD of 37kDa.
The next step was to characterize binding interactions between PotD and its ligand spermidine. This was carried out via tryptophan fluorescence; a technique which detects conformational changes of proteins by measuring changes in the emission spectra of tryptophan residues. Essentially, if there is an interaction occurring between PotD and spermidine, the spectra would shift indicating so.
Figure 5 -
Conclusion and Future Work
In terms of future work, the interaction between PotD and spermidine would need to be characterized more robustly perhaps using other methods such as ITC or SPR. This would help establish binding parameters which would be critical in informing how much protein we would need to put in our device to allow for reliable detection. Once this is achieved, attachment of the fluorescent microspheres would be performed. It would also be ensured that this modification would not interfere with the PotD/spermidine interaction.
↑Saliva
Introduction
A major component which is detectable in saliva is the free iron sequestering compound known as lactoferrin, a protein involved in the innate immune system. Neisseria meningitidis is a gram-negative bacterium with an iron-binding outer membrane protein called lactoferrin binding protein A (LbpA). N. meningitidis uses this LbpA to extract iron from the host lactoferrin under pathogenic conditions to allow for the bacterium to perform essential cellular metabolism such as energy generation and DNA replication.
We predict that purified LbpA would be able to bind to the lacteroferrin present in saliva in vitro. Building on this, we hope it attach a fluorescent molecular probe to LbpA to allow for signal output of bound LbpA (with unbound LbpA washed away from saliva). Here, we aim to overexpress LbpA with a HIS6 tag in E. coli and purify by FPLC and SEC. From here we seek to characterise binding of LbpA to lactoferrin by tryptophan fluorescence and ultimately attach carboxylate fluorescent microspheres to LbpA.
Results
In order to do this chromosomal DNA from Neisseria meningitidis MC58 strain was kindly gifted to us by Dr James Moir from The University of York. This was used as a template for the amplification of the lbpA gene into the pSB1C3 plasmid (BBa_K1590008) and then subcloned into the high expression plasmid pQE80-L.
The pQE80-L – lbpA plasmid was then transformed into M15 pREP4 to allow for more tightly controlled protein expression. E. coli cultures harbouring pQE80-L encoding LbpA were subcultured and grown to an OD600 = 0.6 before being induced with 1mM IPTG. Following 6 hours induction the cells appeared to die as shown in Figure 1.
Figure 1 - LbpA Culture Samples.Lane 1: Sample from uninduced culture. Lane 2: Sample from culture induced with 1 mM IPTG. On comparison of the two cultures, it seems that inducing expression of LbpA causes the cells to die given the significant reduction of protein levels visible on the gel.
In order to investigate this further, we performed plate reader experiments where different concentrations of IPTG were used to induce LbpA expression. The cells were also given a longer period of time to grow. Although cells started to grow again ~7 hours after induction, this was determined to be due to the emergence of mutants.
Figure 2 - Growth Curve of Uninduced and Induced Cultures (0.5 mM, 1 mM and 2 mM IPTG)The graph shows that on comparison with the uninduced control, the induced cultures stop growing when LbpA expression is induced. After ~7 hours, it is possible that the emergence of mutants causes the the OD to rise again or the cells have adapted to the production of the foreign protein.
Despite this, we did try to grow large cultures of M15 E. coli containing pQE80-L-LbpA¬, to see if we could detect any expression. We attempted this under a number of different growing conditions, however, none of these were successful. It is suspected that LbpA forms inclusion bodies and therefore insoluble which makes it difficult to purify.
Future Work
We would continue to try to find the the optimum conditions required to express LbpA and prevent them from forming inclusion bodies. However, we could also prepare and extract the inclusion bodies from E. coli and therefore purify LbpA.
If we were able to successfully purify LbpA we would, as in the case for the other binding proteins, attempt to attach the carboxylate modified fluorescent microspheres to LbpA and characterize its interaction with lactoferrin.
↑Nasal Mucus
Introduction
On the detection of nasal mucus our main protein of focus was the human odorant binding protein 2A (OBP2A). It is a 155 amino acid (excluding the signal peptide) lipocalin of relatively low molecular weight (19318 Daltons). Structurally it is an 8 sheet beta barrel flanked by a c-terminal alpha helix that that together forms an internal hydrophobic pore known as a calix. It is secreted by the olfactory epithelial cells of the nose where it lies in high abundance within nasal mucus. Its primary function in the human body is believed to be in the transport of hydrophobic odorant proteins across the otherwise impenetrable aqueous mucus layer to the olfactory receptors of the nose. Due to its high specificity and abundance within nasal mucus, OBP2A was selected as the protein for use in nasal mucus detection.
Figure 1 - Illustrations of the proposed crystal structure of OBP2A at 2.60 Angstroms. Image: Left shows the 8 strand antiparallel beta barrel in blue. Alpha helix are show in green. Interacting cysteine residues are colored red. Image: Right shows the two different areas of OBP2A that were separated to better understand their interaction, the larger beta barrel is shown in blue and the small c-terminal tail show in red.
In all other aspects of our FluID detector we have targeted a naturally occurring ligand interaction as the basis for subsequent nanobead attachment. In the case of nasal mucus however we were unable to utilize such a pathway as our research suggested that there were no known interactions of high enough specificity for use in the strict detection of nasal mucus. What was our solution? We aimed to separate the alpha helix c-terminal tail of OBP2A and use that as the substrate for fluorescent nanobead attachment. How would that detect the presence of nasal mucus? Through the use of PCR mutagenesis we aimed to improve the binding affinity that the separated c-terminal alpha helix would have for the rest of the OBP2A protein. This in turn we hoped would displace the natively conformed c-terminal tail of OBP2A in exchange for our tighter binding synthetic tail. This synthetic tail could then be attached to a florescent nanoparticle and used in the detection of nasal mucus.
Results
The gene that encodes for OBP2A was first successfuly placed into the pSB1C3 biobrick vector and transformed into E. coli JM110. It is from there that OBP2A was separated into two parts. This was done so that we could first characterize the interaction of the two separated parts and prove that under normal conditions the two constituents would coalesce back into a completed OBP2A protein in vivo. This was done through the use of primers designed to amplify the different sections of the protein that were to be separated. It was decided through observation of the amino acid sequence and through OBP2A crystal structure that a proline at position 118 in the amino acid sequence would be the position of separation for the two parts of OBP2A.
To characterize the interaction between the two separate parts of OBP2A the bacterial two hybrid system (BTH) was implemented and β-galactosidase assays were done. This meant that these separated gene fragments had to be cloned into BTH vectors: pUT18 and pT25. These vectors contain gene fragments for the production of adenylate cyclase (an enzyme that is required for the production of active cyclic-AMP) that becomes active when the integrated gene fragment’s products interact with each other in vivo. This allows us to quantify the interaction through the use of the β-galactosidase assay. Once the gene fragments of OBP2A were successfully cloned into the BTH vectors, both vectors were transformed into MG1655 (Δcya) E. coli strain – a strain that lacks the necessary genes for the production of adenylate cyclase. It was from here that multiple β-galactosidase assays were performed and the miller’s activity( a measure of the level of interaction) was calculated for each control and sample.
Figure 1 - Calculation used to determine the level of interaction between two proteins in vivo.
As of yet these assay have indicated that the two subunits of OBP2A aren’t interacting in vivo. One suggestion as to why this may be the case is that the proteins when separated have exposed hydrophobic residues that cause an alteration of the protein structure of the two parts making them incompatible with each other. It is important to point out however that of the β-galactosidase assays that were done all of them have had controls that have failed to function, so it is impossible at this stage to definitively tell that the two separated parts of OBP2A aren’t interacting in vivo.
Figure 1 - Above, illustrates the calculated miller’s activity of each control/sample and suggest that the OBP2A subunits aren’t interacting. As can be gauged from the sample on the far right of each graph. They suggest that OBP2A has a lower interaction than the negative and regulatory controls.
Conclusion and Future Work
The next stage of experimentation we aim to do is to have repeated the beta-galactosidase assay, using more and better controls to eliminate the current issues that the assay are having with failed controls. Along with this we also aim to clone the two parts of OBP2A into the BTH vectors but in the opposite vectors to see if that has any effect on the interaction of the two parts of OBP2A. If this had shown considerable change in the level of interaction between the two parts of OBP2A then we would have to reconsider the use of bacterial two hybrid as the method for determining protein interaction.
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