Investigation of Interaction of Vaccinia Virus Complement Control Protein and Curcumin with Complement Components C3 and C3b Using Quartz Crystal Microbalance with Dissipation Monitoring Technology

INTRODUCTION

Complement regulatory molecules might prove beneficial in the prevention of damage to the central nervous system (CNS) from up-regulated complement components in chronic as well as acute neurodegenerative disorders. With the objective of investigating small molecules with an ability to regulate the complement system, VCP was compared to phenolic hydroxy compounds of herbal origin, rosmarinic acid (RA), quercetin (Qur), and curcumin (Cur) by using in vitro techniques [1]. In the past two decades, VCP has been thoroughly investigated for its effect on components of the complement system. VCP was reported to inhibit both the classical pathway (CP) and the alternative pathway (AP) two decades ago [2-4]. It was found to inhibit these pathways by binding to the third and fourth components of the complement [3, 4]. VCP is known to be structurally similar to C4B binding protein (C4Bbp), but functionally to CR1, a human complement regulatory molecule known to bind C3b. VCP has previously been shown to bind to C3b using surface plasmon resonance (SPR) [5]. Similar to VCP, Cur was found to inhibit both the CP and AP of complement activation [5]. It is possible that it may also inhibit these pathways through its ability to interact with C3b. Previously, Cur was shown to inhibit the AP activation. It was proposed to show this activity through its ability to prevent the cleavage of factor B to Bb [1]. It was hypothesized that it might have done so either through binding to Mg⁺⁺, or through binding to factor D which cleaves factor B to generate Bb fragments. It was also proposed that it might be able to inhibit the formation of C3 convertases. It may inhibit stabilization of C3 convertase by properdin or it may have more than one site of action on the complement components. The complement components that Cur might bind could be the one central to the activation of CP and AP. Properdin can bind to C3 (H₂O) and C3b for the assembly of the C3 convertase. Complement factor B and Bb bind to C3 (H₂O) for the formation of C3 convertase [6].

Based on our previous results [1] it can be proposed that Cur may bind to C3 (H₂O) and/or C3b. By doing so, it may prevent binding of properdin or Bb to C3 and C3b, and thereby inhibit the formation of the AP convertase. C3 in the form of C3 (H₂O) also acts as a central component of complement activation, which circulates in the body in its inactive form. Upon activation, it is converted into its active fragments such as C3b, C3a, C3c and C3d as discussed in several reviews [7, 8]. C3b and C3a are reported to play a damaging role in inflammatory disorders. HIV and its proteins are known to increase the expression of C3 in the neurons and astrocytes [9]. Recently, it was also proposed that HIV uses complement opsonin iC3b, a C3b or C3 fragment, and this opsonized HIV infects T cells [10]. Highly active anti-retroviral therapy (HAART) which is commonly used to treat HIV infections is associated with peripheral neuropathy and elevation of complement components C3 and C4 [8, 11]. C3 is also implicated in several neuroinflammatory disorders. C3 and C4 are expressed in C1q sufficient and deficient mice [12]. The levels of C3 and C4 are also elevated in Alzheimer’s disease with mild to severe clinical symptoms with a low level of expression of complement regulatory molecules [13]. Therefore, there is little doubt that the activated complement components need to be regulated and compounds inhibiting C3 and C3b need to be discovered to prevent the detrimental effects of these complement components. VCP is known to inhibit both C3b and C4b. However, VCP’s ability to bind to C3 has not been reported. Similarly, Cur’s ability to bind C3 and C3b has also not been reported. It was therefore considered important to investigate and compare the effect of these components central to the activation of complement by use of specialized techniques.

There are many techniques available for protein adsorption or interaction as cited by Ramsden [14] and Höök [15]. In order to carry out the protein binding study, it was decided to use QCM-D based Q-sense (D-300), a Swedish based technology thoroughly studied and developed for the protein adsorption studies at Chalmers University of Technology, Goetborg, Sweden. The information provided and cited in Hööks thesis and investigations by some other authors are briefly discussed here [15].

COMPARISON OF Q-SENSE WITH OTHER TECHNIQUES

In order to study protein-protein (P-P) or protein-surface (P-S) interaction / adsorption, many techniques based on various working principles are available. The most extensively used techniques being Optical Wave guided Laser Spectroscopy (OWLS), Ellipsometry (ELM), Surface Plasmon Resonance (SPR), Enzyme Linked Immunosorbent Assay (ELISA), Circular Dichroism (CD), Fourier Transform-Attenuated Total Reflection-Infrared Spectroscopy (FT-ATR-IR), and Quartz Crystal Microbalance (QCM). The first three techniques are based on the principle of optometry; ELISA is a labeling technique; CD is based on the spectroscopic measurement of the differential adsorption of the polarized light; FT-ATR-IR is based on infrared spectroscopy, and QCMD is based on electrical measurements. In Q-sense D-300, which is based on the QCM-D principle, the change in frequency (dF) of a quartz based sensor crystal (i.e.,coated either with a very thin layer of gold or other metals; the gold coated quartz crystals were used for the current investigation) resonating at its resonant frequency (f) upon adsorption of an adsorbing moiety (AM) is correlated with the change in mass of AM. The energy dissipated during this adsorption is also recorded and measured in terms of dissipation factor (D). The changes in dissipation (dD) and dF are specific for a particular system comprising an AM. The ratio dD/dF gives information regarding the viscoelastic property and adsorption kinetics of a system [15].

The comparison of QCM-D and the most extensively used techniques for the P-P and P-S interactions such as SPR, ELM, and OLWS [16] as well as a summary of other available techniques for these studies is thoroughly reviewed by F Hook of the Götenberg University [15]. The information regarding other techniques used for P-P and P-S studies is also readily available in the literature. Each technique has certain advantages and disadvantages and selection of a technique depends upon the information required. Recently QCM-D (Q-sense D300) and SPR (BIACORE) were explored to study the interactions between a peptide antigen (IA-2) and a polyclonal antibody raised against this peptide [17]. The combined data from both these techniques was shown to be effective in reducing the nonspecific binding of the antibodies in sera and detect the antigen at about 0.2 nM. Both these non-labeling techniques were found to be comparable to other labeling techniques and offered an advantage of real time monitoring [17]. SPR and QCM-D were also compared in the study of whole blood and plasma coagulation [18]. Both the techniques concluded that blood coagulation is a bulk process and not a surface phenomenon. These techniques were also found to sense the changes in the coagulation process after the addition of activators and inhibitors of blood coagulation. QCM-D has also been compared with the OWLS and ELM for a P-S interaction study [16]. All these techniques were found to be suitable for the kinetics of protein adsorption. The OWLS and ELM directly gave the information regarding mass (dry) of the adsorbed protein, whereas QCM-D gave information regarding the mass of the protein as well as water hydrodynamically coupled to the protein adlayer or bound to the protein. QCM-D also gave additional information regarding the viscoelastic property through the energy of dissipation (D) of the adsorbed layer of protein. This information can be used to obtain detailed information regarding the conformational changes associated with the protein adsorption. QCM-D is based on the principle of QCM with an advantage over QCM and the optical techniques as it gives additional information regarding the rigidity of the binding and possible conformational changes associated with the binding. When QCM was compared with a licensed HIV-ELISA, a labeling technique, its sensitivity was found be comparable to that of ELISA system [19]. The real time monitoring and short duration for detection (10 min vs minimum of 2 h for ELISA) are the advantages of QCM over ELISA. QCM-D was combined with ELISA to study interaction of fibrinogen with an antifibrinogen monoclonal antibody [20]. The absorbance ratios for pH dependent denaturation of fibrinogen obtained using ELISA were comparable to the pH dependent changes in mass of the adsorbed protein or changes in thickness of fibrinogen layer under various pH conditions measured by QCM-D. This combination was also found to reveal information regarding the changes in conformation of fibrinogen adlayers upon interaction with the anti-fibrinogen monoclonal antibody.

From this discussion, it can be concluded that QCM-D is comparable to the other extensively used techniques to study the P-P and/or P-S interactions. It however offers advantages of real-time monitoring, rapidity, sensitivity, simultaneous detection of viscoelastic properties and mass of the protein layer, and gives additional information regarding the structural and/or conformational changes associated with the protein adsorption.

Under in-vivo conditions, the biological systems such as protein molecules or small sized molecules would interact with each other in their hydrated state. Therefore for appropriate simulation of the in-vivo interactions of the biomolecules such as VCP, tVCP, and Cur with that of the complement system, the information regarding the in-vitro interaction studies of these compounds with the complement components under hydrated conditions would give additional information. For the aforementioned reasons, and the advantages of QCM-D over the other techniques mentioned previously, QCM-D was thought to be the most appropriate method for the current investigation which involves comparison of the P-P, P-S interactions as well as interactions of proteins and small sized molecules.

PREVIOUS STUDIES WHERE QCM-D WAS USED FOR STUDIES RELATED TO THE COMPLEMENT SYSTEM

QCM-D has previously been employed to study the interaction of the complement system with biomaterials. J. Andersson from the University of Uppsala, Sweden studied the interaction of complement components with that of biomaterial surfaces [21]. Using QCM-D, it was shown that the polystyrene surface activates the AP of complement activation. C3 deposited on the polystyrene surface can form C3 convertase and activates the AP of complement activation [21]. QCM-D was also compared to ELISA technique to show that biomaterial surfaces activate the complement system and this activation can be inhibited by complement regulatory molecules such as factor H [22]. Thus Q-sense based on QCM-D may be employed to investigate the complement regulatory molecules of therapeutic importance. In order to confirm binding characteristics, more than one surface should be used to ensure proper comparison.

In the current study the gold and polystyrene sensor (PS) crystals were used to study the interaction with the complement system in hydrophilic and relatively hydrophobic environments, respectively. PS crystals are prepared by applying thin coatings of polystyrene onto the gold coated quartz crystals. PS surface is known to activate the complement system via C3 offering a special advantage in the study. Cur is known to interact with bovine serum albumin (BSA) [23, 24] and therefore BSA was used as a positive control for the interaction of Cur with C3 and C3b.

Q-sense: Practical Considerations [15 and Q sense manual]

The equipment used for the current investigation Q-sense (model D-300) makes use of QCM-D technology as discussed above. It consists of four basic components viz. the electronic unit (A), measurement chamber (B), sample holder (C), and the UV chamber for activating the sensor crystal surface (D); (Fig. 1).

In most of the Q-sense based experiments, temperature needs to be controlled appropriately by use of the controller knob of the electronic unit. The experiments are carried out at room temperature (+25 ˚C) as extremes of temperature may induce aberrant changes in frequency. The temperature inside the chamber for all the experiments was maintained at 24.7 ˚C. Inside this chamber (Fig. 2), the AT-cut crystals (gold or polystyrene coated; Fig. 3) operated in thickness shear mode at 5 MHz were mounted as per the instructions in the manual.

The smooth surface of the crystal is used for the measurements, and the opposite side of the crystal is connected to A/C supply of the electrical unit and operated in a shear thickness mode. The measurement chamber also consists of a sample holder, the position of which can be adjusted to optimize the flow rate. The solution of the AM is kept in this sample holder and it can either be added to the “temperature loop” or to the “sensor crystal” using a controller knob on the measurement chamber. About 2 ml of solution is passed onto the sensor crystal for an accurate measurement.

The chamber is connected to a PC and the change in f and D is monitored online at different overtones using q-soft software. The q-tools software provided with the equipment is used for the analysis of the data captured using q-soft. Using q-tools, it is first confirmed whether the adsorption of AM follows the Sauerbrey law using fit analysis. If the adsorption doesn’t follow the Sauerbrey equation, a method called Z-match and/or viscoelastic modeling is recommended. As discussed earlier, the change in frequency upon adsorption is correlated with the mass adsorbed on the sensor crystal to study the adsorption of AMs used in the study.

Terminology Used in the Results and Discussion

As discussed in the above section, there were two to three AMs used for the study. AMI = AM bound to the surface of the sensor crystal (gold or PS). Therefore, AMI is indicated by putting the first letter of the surface (g = gold; ps = polystyrene) in lower case, next to AMI. The abbreviations used in the results and discussion are as mentioned below:

1. Where AM is bound to the surface of the sensor crystal (AMI), where it is either gold or PS, the abbreviations are VCPg, VCPps, tVCPg, tVCPps, C3g, C3ps, C3bg, C3bps, BSAg, and BSAps.
2. Where AMII is bound to AMI bound to the surface of the sensor crystal (g or ps) as shown in the table 3.1, the abbreviations are C3-VCPg, C3-VCPps, Cur-C3g, Cur-C3bps, etc.
3. Where AMIII is bound to the AMII adsorbed onto AMI as described above and shown in the table 3.1, the abbreviations are Cur-C3VCPg, Cur-C3VCPps, Cur-C3tVCPg, etc.

Most of the experiments were carried out for 30 min, therefore, dF₃₀ and dD₃₀ refers to dF and dD values after 30 min, respectively. dF₃₀ and dD₃₀ values for AMs were calculated as follows:

1. dF₃₀ = dF at 30 min – dF_initial, where dF_initial refers to the baseline or initial f or D values prior to the adsorption of AMs.
2. In some of the experiments, the adsorption was continued for more than 30 min (and rarely less than 30 min). In those cases, in addition to dF₃₀ or dD₃₀ values, dF_fin or dD_fin values were also calculated. These values were recorded after washing the surface with PBS after the adsorption was over and were calculated as: dF_fin (or dD_fin) = Final dF (or dD) values after washing with PBS – dF_initial (or dD_initial).
3. Using these dD and dF values, dD/dF ratios were calculated to get the information regarding the rigidity (affinity) or viscoelasticity of binding.
4. No. of molecules of AM adsorbed onto the crystal surface or onto the other AM = 6.022 X 10²³ X mass adsorbed (ng/cm²) / molecular weight of the AM.
5. Molecular weights of C3, C3b, Cur, BSA, and tVCP in nanograms (ng) were 1900 X 10¹¹, 1800 X 10¹¹, 3.6839 X 10¹¹, 680 X 10¹¹, 188 X 10¹¹, and 288 X 10¹¹, respectively. These values were taken either from Calbiochem catalogue (C3 and C3b), Sigma-Aldrich (Cur) or from the literature (VCP and tVCP).

Guide to the Interpretation of the Figs. (4 to 7)

These figures comprise both the primary and secondary axes. The primary X and Y axes are shown by solid black lines, whereas the secondary X and Y axes are shown by ultrafine hatched black lines. The primary X axis represents AMs (Please refer to the terminology section above for the meaning of the abbreviations used for AMs). The primary Y axis shows dD/dF ratios for AMs shown on the primary X axis. Two different sets of dD/dF values for the AMs are shown by solid black bars and hatched bars. The solid black coloured bars indicate the average values after 30 min (dD_30avg/dF_30avg) and the hatched bars indicate the average final values after washing the sensor surfaces once the experiments have been completed (dD_Finavg/dF_finavg). The secondary Y axis represents dF values for the AMs shown on the primary X axis. The gradient black bars plotted on the secondary X and Y axes represent dF₃₀ values. The dF₃₀ values are also displayed on the secondary axis for a quick reference. The gradient black dots connected by a hatched black line are used to show the dFfin values of AMs on the primary X axis. It should be noted that for some of the AMs, dF₃₀ or dFfin values plotted on the secondary X axis of these graphs were high and the bars for these values were overlapping with the dD/dF bars plotted on the primary axis, when ‘zero’ was used as the point of origin. In order to avoid this overlapping, the point of origin of the graphs is a negative value although such negative values do not have any physical reality VCPhc refers to VCP used at a higher concentration.

Guide to the Interpretation of the Figs. (8 to 10)

In order to discuss the results of the kinetics of binding of AMs, dD values (Y-axis) at five different time points were plotted against dF values (X-axis) at the same time points. dD vs dF graphs are plotted to avoid time dependency and to understand the shapes of the graph in order to study the phases and kinetics of adsorption. Therefore the zero values used in the current graphs indicate neither time points nor do these values indicate data points. The zero values are however used to get information regarding the slope of the graph during the first phase of adsorption (zero to 1 min). The adsorption during this period in some of the cases is rapid whereas it is relatively slower in some other cases. In order to get a comparative account of kinetics of adsorption of different AMs during this first phase of adsorption, it was considered necessary to use ‘zero’ as the point of origin for these graphs.

RESULTS

DISCUSSION

QCM studies correlate dF values with that of the mass of a moiety adsorbed based on the Sauerbrey relation as discussed in the principle of QCM. The adsorption of a protein layer on the crystal surfaces may violate the Sauerbrey relationship [15, 28, 29]. The mass adsorbed cannot be estimated using the dF values in those cases [15, 30]. However, the frequency shift can reliably be interpreted using another factor called dissipation or D factor [15, 25]. Therefore in QCM-D, in addition to dF values, the most important factor that can be studied is the factor D which provides information regarding the rigidity of protein binding. dD/dF ratios have been used previously to investigate the rigidity of protein binding [15, 26, 27]. These ratios were also defined as K values (K = dD/dF) by Ayela C. et al. [17]. All these studies show inverse correlation between the ratio and rigidity of the binding, i.e, the lower the ratio for the P-P or P-S binding, the stronger is the binding. The dD/dF ratios for the adsorption of VCP on C3ps in the current investigation were found to be very low; consequently a very strong binding of VCP with that of C3ps is indicated. Using SPR, it is established that VCP inhibits the complement system through its ability to bind to C3b [5]. The current findings have added a new dimension to the mode of action of VCP. VCP and tVCP were used at two concentrations in the current study. At lower concentration (2 nm), the amount of VCP adsorbed on C3 was about 670 ng/cm² with dD_fin/dF_fin ratio corresponding to about 0.0099, whereas the amount of C3 adsorbed on tVCP was about 587.46 ng/cm² with dD/dF ratio of 0.0110 suggesting that VCP binds more strongly to C3 than that of tVCP. When the concentration of VCP was increased by 1.25 times (VCPhc), the amount of VCPhc adsorbed on PS was significantly higher than that of VCP at a low concentration (not shown here). Also, VCPhcps shows adsorption kinetics and the pattern of adsorption different from that of VCPps (not shown), suggesting that both the adsorption kinetics and pattern of adsorption are concentration dependent for VCP. This might be due the ability of VCP to form a dimer as shown by the others [31].

When the binding of VCP and tVCP to C3 was compared on the PS surface, dD/dF values for C3-VCPps were less by as much as twice then that for tVCP. However, the amount of C3 adsorbed on them were found to be the nearly the same (Fig. 4).

The dD/dF ratios for the adsorption of Cur on C3 were greater than that for the adsorption of C3 on VCP and tVCP, but about 2.8 times smaller than that of Cur-BSAps (Fig. 4). Similar results were observed on the gold surface (Fig. 5). dD₃₀/dF₃₀ ratio for Cur-C3g binding was three times less than that of Cur-BSAg. Cur showed greater affinity for C3g than that of C3ps. However, a greater amount of Cur was adsorbed on C3g than that of C3ps. Also, on both the gold and PS surfaces, the amount of Cur adsorbed on C3 was more than that on BSA. Previous studies have shown that BSA binds to Cur [20, 21], and therefore BSA was included as a positive control in the current study. The dD/dF ratios were more for Cur-BSA that that of Cur-C3, and the amount of Cur adsorbed onto C3 was also more than that onto BSA. Therefore, from the outcome of the current investigation, it is concluded that Cur shows stronger binding affinity for C3 than for BSA.

The dD/dF ratios for VCPps-C3b and tVCPps-C3b did not differ significantly from each other (Fig. 6). This suggested that both VCPps and tVCPps have an equal affinity for C3b at the concentration used in the study. Previous studies using SPR revealed that tVCP does not bind to C3b [4]. This could be attributed to the difference in the concentration used, and variation in their methodology. They used amine coupling, as opposed to the adsorption onto PS. The dD/dF ratios for C3b-VCPps and C3b-tVCPps were significantly higher than that of C3-VCPps and C3-tVCPps (Fig. 6). This suggested that both VCP and tVCP show greater affinity for C3 than that for C3b on PS. On the gold surface, the amount of C3 adsorbed onto VCPg is three times more than that for tVCPg (Fig. 5).

The dD/dF ratio for C3b-VCPg was found to be approximately 2.8 times less than that of C3b-tVCPg, and the amount adsorbed in ng / cm² was found to be about three times more for C3b-VCPg than that for C3b-tVCPg. These results suggested that VCP binds to C3b to a greater extent than that of tVCP. These results, as opposed to the study on PS, compare with the findings by Smith et al. [4] where they have shown binding of VCP to C3b using SPR. The dD/dF ratios for the adsorption of C3b onto VCP and tVCP bound to the gold and PS surfaces were found to be more than that for C3 on both the surfaces. This suggests that both VCP and tVCP bind to C3 more strongly than that of C3b. VCP binds to C3 and C3b to a greater extent than that of tVCP.

When Cur was tested for its ability to bind to C3bps, dD/dF ratios for Cur-C3bps was found to be less than that for Cur-BSAps, which suggested stronger binding of Cur to C3bps. However, dF values as well as the amount of Cur adsorbed onto C3bps was less than that of BSAps (Fig. 6). The results were similar for the adsorption of Cur on C3bg and BSAg, where the dD/dF ratio was found to be less for Cur-C3bg and the amount in ng/cm² of Cur adsorbed on C3bg was less than that on BSAg (Fig. 7). The results indicate that Cur binds to C3b with more affinity, but the binding is weaker than that of Cur-C3. These findings suggest that inhibition of the CP and AP shown by Cur using the haemolysis assay and the Quidel kit [5] could therefore be attributed to the ability of Cur to bind to both C3 and C3b, but it binds to C3 with greater affinity than to C3b.

In previous studies [26, 27], dD and dF values at different time points were plotted on a X-Y scatter plot to give information regarding the binding kinetics of AMs. These X-Y scatter plots gave information regarding the phases of adsorption, which in turn provides insight into the nature of adsorption, molecular arrangement or change in conformation during adsorption which might have an impact on the adsorption of the second AM. Therefore, in the current investigation, dD vs dF graphs were plotted to get information regarding binding kinetics of the AMs.

The adsorption kinetics for the interaction of VCP and tVCP with that of C3 and C3b adsorbed onto the gold and PS surfaces is shown in Figs. (8 and 9), respectively. As shown in Fig. (9), C3 adsorbs in two phases, with the exception of C3-VCPhcps. In all the cases for the adsorption of C3 on VCP and tVCP on both the PS and gold surfaces, the dF values for the last data points are more than -140 Hz (except for VCPhcps; Fig. 8), and that for the adsorption of C3b on tVCP and VCP, on PS and gold surfaces, being less than -40 Hz, except for C3b-VCPps (Fig. 9). The adsorption kinetics also suggests that dD values per unit change in dF values are quite high for the adsorption of C3b on both VCP and tVCP (Fig. 9).

The adsorption kinetics for the adsorption of C3 and C3b on VCP and tVCP suggest that both VCP and tVCP have better affinity for C3 than that of C3b (Figs. 8 and 9). C3b shows better adsorption kinetics for VCP than that of tVCP. The lack of module one in tVCP as well as structural difference between C3 and C3b may be attributed to the differences in the adsorption kinetics of these AMs.

The adsorption kinetics for the adsorption of Cur on C3 and C3b adsorbed onto PS and gold surfaces, is shown in Fig. (10A). As shown in the results section as well as Fig. (10A), the dD values per unit change in dF values are higher for Cur-C3 and Cur-C3b adsorption than that for VCP and tVCP (Figs. 8 and 9).

When Cur was adsorbed onto C3 (Fig. 10B) and C3b (Fig. 10C) bound to VCP or tVCP, there was a sharp increase in dD values, and the values were on the higher side for Cur-C3tVCPps/g (or Cur-C3btVCPps/g) than that of Cur-C3VCPps/g (or Cur-C3bVCPps/g). For Cur-C3bVCPps the final dD values were the same as that of Cur-C3bps with a greater decline in dF values. Similarly, the adsorption kinetics pattern and the final dD values for Cur-C3VCPg were quite close to Cur-C3g. This could be attributed either to an enhanced binding ability of Cur to C3 and C3b bound to VCP, or both VCP and Cur share different binding sites on C3 and C3b which might have resulted in similar dD values in the respective cases. In the case of adsorption of Cur on C3 and C3b bound to tVCP, there was a sharp rise in dD values suggesting a very loose binding of Cur. This could be due to sharing of common binding sites by tVCP and Cur.

The mass of AMs adsorbed onto the other AM or onto the gold or PS surface in the QCM-D, could be used to estimate the number of molecules of the binding moieties interacting with each other. In the current investigation, using the Avogadro’s formula, the number of molecules interacting with each other is not reported as these estimated values are not accurate as the exact mass of water trapped within the AMs used in the study is unknown. Generally about 30 % of water is trapped within the proteins [26, 32]. Consequently, this 30 % value was deducted from the final mass of AMs adsorbed onto various surfaces and the other AMs obtained in the current studies. However, water trapped within Cur molecules as well as VCP, and tVCP is not known. Further research is required in this direction. QCM-D could be coupled with the other techniques such as ELM or OWLS to get information regarding the dry mass of the adsorbed compounds, and thereby the information regarding the water bound to protein or protein adlayer could be abtained [16].

In the case of Cur, dD values were very high in some of the experiments which violate the Sauerbrey law, and therefore the exact amount of these compounds interacting with each other could not be determined.

However, the dD/dF ratios and other information reported in this investigation certainly have implications in the development of complement based pharmacotherapeutic agents in the treatment of neuroinflammatory disorders. The binding of VCP and Cur to C3 and C3b found in the current investigation can be correlated with the complement inhibition by them shown previously [1]. VCP was found to be thousand times better than that of Cur in inhibiting the complement mediated haemolysis, and this could be attributed to a better ability of VCP to bind both to C3 and C3b than that of Cur as observed in the current investigation. tVCP, which inhibited the CP to a lesser extent could be attributed to the fact that although it adsorbs onto C3 and C3b, the binding is variable, and it does not bind to C3 and C3b as strongly as VCP.

As discussed in the introduction, a polystyrene surface activates C3. VCP, tVCP as well as Cur were able to inhibit the same. These compounds inhibited C3 to a greater extent than that of C3b.

In conclusion, in the current study, QCM-D was successfully employed to obtain information regarding the interaction of VCP, tVCP, and Cur with C3 and C3b. VCP showed greater binding affinity for both the C3 and C3b than Cur and tVCP. The binding of VCP and tVCP to C3 and C3b was orientation dependent. In addition, it was shown that Cur binds to both C3 and C3b. However, all these compounds show greater affinity for C3 than C3b. VCP is a thousand fold stronger inhibitor of complement than Cur, and is known to inhibit amyloid mediated complement activation [33]. Cur is a weak inhibitor of complement, but dissolves plaques [34]. The current investigation suggests that both VCP and Cur probably share different binding sites on C3 and C3b, and thus may not interfere with each others actions on the complement system. Due to their broad spectrum anti-inflammatory activities covering different aspects of inflammation, and possibility of sharing different binding sites by them as discussed above, further research is recommended in the direction of developing a combination therapy or “synergistic cocktail” by mixing Cur and VCP to prevent the complement mediated neurodegeneration in amyloidopathies. Just like curcumin, many other small sized complement regulatory molecules could be exploited to study the mode of complement inhibition by them using QCM-D technology. Polyhydroxy phenolic compounds, terpenes, esters, and the compounds of natural origin belonging to different chemical classes thoroughly reviewed in a recent article [1] could also be investigated for the complement regulatory activity by them. These compounds may inhibit various stages of activation of the complement system and could be used to develop combinatorial therapy to treat disorders of the brain where the complement system is activated. The same technology could also be used study the interaction of these molecules with other receptor molecules as well. The current investigation has shown that QCM-D could be applied to develop a better understanding of complement regulatory agents with therapeutic effectiveness.

REFERENCES