Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane

Hirose, Masanori; Sugisaki, Shigenori; Suga, Keishi; Umakoshi, Hiroshi

doi:https://doi.org/10.1155/2019/4926435

Journal of Chemistry

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Abstract Introduction Materials and Methods Results and Discussion Conclusions Abbreviations Data Availability Conflicts of Interest Acknowledgments References Copyright Related Articles

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Nanotechnology for Food Engineering: Biomembrane and Nanocarriers

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Research Article | Open Access

Volume 2019 | Article ID 4926435 | https://doi.org/10.1155/2019/4926435

Detection of L-Proline-Catalyzed Michael Addition Reaction in Model Biomembrane

Masanori Hirose,¹Shigenori Sugisaki,¹Keishi Suga,¹and Hiroshi Umakoshi¹

Academic Editor: Josefina Pons

Received03 Oct 2018

Revised26 Dec 2018

Accepted10 Jan 2019

Published26 Feb 2019

Abstract

A method to detect the L-proline- (L-Pro-) catalyzed Michael addition reaction in model biomembranes has been established, using N-[p(2-benzimidazolyl)phenyl]maleimide and acetone as reactants. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy. The kinetics of the reaction were different from those of the constituent lipids of the liposomes. Zwitterionic 1,2-dipalmitoyl-sn-glycero-3-phosphocholine liposome, which is in the solid-ordered phase, had a better value of reaction rate, suggesting that the reaction rate constants of this reaction in liposome membrane systems could be regulated by the characteristics of the liposome membrane (i.e., the phase state and surface charge). Based on the results obtained, a plausible model of the L-Pro-catalyzed Michael addition reaction was discussed. The obtained results provide us with an easily detectable method to assess the reactivity of L-Pro in biological systems.

1. Introduction

L-Proline (L-Pro) is one of the principle amino acids that are the building blocks of proteins. L-Pro is known to elucidate various kinds of physiological activities though its interference in the metabolic pathway, such as in the enhancement of growth of epidermal cells, activation of collagen biosynthesis, repair of damaged collagen, and moisture of the stratum corneum [1]. Considering these physiological activities, the use of L-Pro as a possible key material in food engineering has become significant.

As another significant aspect of L-Pro, it is gaining attention as an organocatalyst [2, 3]. With respect to safety and high efficiency, the use of L-Pro will prove beneficial in industrial processes, such as in the manufacture of medicine and food. Barbas and coworkers have reported many examples of L-Pro-catalyzed reactions, especially focusing on enantioselectivity [4–6]. The L-Pro-catalyzed reaction is usually achieved through the formation of the “enamine” intermediate, between L-Pro and the ketone substrate. It is known that most of reported reactions have been carried out in the polar solvent, e.g., dimethyl sulfoxide (DMSO), but not in the high-polar solvent such as water, owing to the stability of the enamine intermediate. Considering the use of L-Pro in food engineering, it is thought that there could be some risks of the side reaction induced by L-Pro, as a less polar (hydrophobic) environment would exist in a biological system (e.g., in the interior of a biomembrane).

Recent studies have also focused on the use of self-assembly systems in organic synthesis because self-assemblies enable insoluble materials dispersed in aqueous media [7]. The liposome, a vesicular envelope composed of a phospholipid bilayer membrane, is known as a model of biomembranes. It can also be utilized as a platform of organic synthesis in aqueous media [8–11]. The liposome surface properties can be customized by modifying the lipid composition [12]. The combined use of small molecules with liposomes would lead to a cooperative alteration in the membrane properties, which can contribute to providing improved functions such as chiral recognition [13]. While the liposome structure has to be disrupted to recover the reaction product for its analysis, the use of the fluorescent reactant, for example, N-[p(2-benzimidazolyl)phenyl]maleimide (BIPM) [14], enables us to directly determine the reaction rate constant.

Previously, we have observed that L-amino acids, including L-Pro, can bind onto liposomal membranes [13]. Thereby, the L-Pro-catalyzed reactions can proceed on liposome membranes in aqueous media [9, 11]. However, some challenges are still encountered in directly monitoring the kinetics of L-Pro-catalyzed reactions in the aqueous medium because the product is basically analyzed after extraction and purification. In this study, the L-Pro-catalyzed Michael addition reaction of BIPM and acetone was employed because BIPM is reported to be a good substrate to monitor L-Pro-catalyzed reactions through the fluorescence of the product [14]. The effect of liposome membranes on this reaction was kinetically analyzed using fluorescence spectroscopy. Based on the results obtained with previous findings, finally, a plausible model of the L-Pro-catalyzed Michael addition reaction was discussed. The obtained results provide an easily detectable method to assess the risk of L-Pro in biological systems.

2. Materials and Methods

2.1. Materials

1,2-Dipalmitoyl-sn-glycero-3-phosphocholine (DPPC: C16 : 0, zwitterionic), 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC: C18 : 1, zwitterionic), and 1,2-dipalmitoyl-3-trimethylammonium-propane (DPTAP: C16 : 0, cationic) were purchased from Avanti Polar Lipids, Inc. (Alabaster, AL, USA). L-Proline (L-Pro) and D-Proline were purchased from Peptide Institute (Osaka, Japan). N-[p(2-benzimidazolyl)phenyl]maleimide (BIPM) was purchased from Tokyo Chemical Industry co., Ltd. (Tokyo, Japan). Other chemicals were purchased from Wako Pure Chemical Industry Ltd. (Osaka, Japan) and were used as received.

2.2. Liposome Preparation

Liposomes were prepared based on literature [9]. In brief, a chloroform solution of lipids was dried in a round-bottom flask by using a rotary evaporator. The lipid film was dissolved in chloroform, and then the solvent was removed. The obtained lipid thin film was kept in a vacuum chamber for at least three hours, to remove the solvent completely. The dried lipid film was hydrated with ultrapure water at 60°C. The liposome suspension was frozen at −80°C for 15 min and was thawed at 60°C for 15 min. This freeze-thaw cycle was repeated for five times. The liposome suspension was finally treated by using the extrusion device (Lipofast; Avestin Inc., Ottawa, Canada), with two layers of polycarbonate membranes with a mean pore diameter of 100 nm. The size distributions of liposomes were determined by dynamic light scattering (DLS, Zetasizer Nano ZS, Malvern Panalytical, Grovewood Rd, UK). The average size of DPPC liposome just after preparation was 172.9 nm (PDI: 0.224). The average sizes of acetone added liposomes after 0 and 2 h were 143.3 and 247.3 nm, respectively, revealing that the addition of acetone resulted in only small influences on the liposome structures.

2.3. Kinetics of L-Pro-Catalyzed Reaction in DMSO/Water System

L-Pro-catalyzed Michael addition of BIPM (BIPM: 28.9 µg (0.1 µmol)) with acetone (0.2 mL (2.7 mmol)) was conducted in DMSO or aqueous solution. L-Pro-catalyzed reaction was initiated by adding 10 µl of stock solution of BIPM (10 mM) in acetonitrile (CH₃CN)/DMSO (1/1 v/v) mixture and 10 µl of stock solution of L-Pro in water (0–8 mM) and acetone (200 µl) to 780 µl of DMSO or aqueous solution. The reaction was carried out in a quartz cell for measurement without stirring. The background fluorescence (before the reaction) was weak enough, and the increased fluorescence intensities were measured by the fluorescence spectrophotometer FP-8500 (JASCO, Tokyo, Japan) at 25°C. The samples were excited with 315 nm and measured at 362 nm. The reaction kinetic was considered by first-order kinetics, and the reaction rate constant, k, was determined by following equation:where and represent the fluorescence at arbitral time () and the final fluorescence intensity, respectively. The products were analyzed by HPLC (Waters 1500 HPLC System (Waters, Milford, MA, USA) equipped with the ODS2 column (25 cm) (GL Science Inc., Tokyo, Japan)). Mobile phase was prepared with CH₃CN/0.1% aqueous trifluoroacetic acid (15 : 85) at a flow rate of 1.0 mL/min, with detection at 310 nm. The retention times of BIPM and product are 30.1 and 28.9 min, respectively.

2.4. L-Pro-Catalyzed Reaction in Liposome Membrane

L-Pro-catalyzed reaction in the liposome membrane was initiated by adding 10 µl of stock solution of BIPM (5 mM) in CH₃CN/DMSO (1/1 v/v) mixture and acetone (200 µl) to a 790 µl of mixture of liposome and L-Pro. A mixture of liposome and L-Pro was preincubated by mixing 780 μl of the liposome membrane (5 mM) and 10 μl of L-Pro stock solution of water (100 mM). The reaction was carried out in 5 ml of the screw vial with stirring and light shielding. A sample for fluorescence measurement was prepared by diluting the reaction solution 50-fold with water. HPLC analyses were carried out as described above.

3. Results and Discussion

3.1. L-Pro-Catalyzed Reaction in DMSO and Water

BIPM is reported to be a good molecular probe to monitor the L-Pro-catalyzed reaction because its product shows fluorescence [14]. First, the L-Pro-catalyzed Michael addition reaction of BIPM and acetone (Scheme 1) was performed in DMSO. In the available literature, the reaction rate of the Michael addition reaction of BIPM and acetone, catalyzed by L-Pro, has been reported as 0.005 μM/min [14]. The 24-hour incubation period could be long enough to reach saturation in these reaction media. Figure 1 shows the fluorescence spectra of the products obtained in DMSO and water with an incubation period of 24 hours. The emission peak wavelength of the product could be dependent on the solvent; the wavelengths in DMSO and water were 360 nm and 368 nm, respectively. In the 1,2-dioleoyl-sn-glycero-3-phosphocholine (DOPC) liposome system, the emission peak was observed at 372 nm and the fluorescence intensity was slightly higher than that obtained in water. The fluorescent properties of the products are further discussed in Section 3.4. These results revealed that the product can emit strong fluorescence in these media.

In general, the L-Pro-catalyzed Michael reaction is faster in DMSO [3, 9]. The dependence of amount of the catalyst in this reaction was then investigated by varying the amount of L-Pro. Figure 2(a) shows the time course of the fluorescence intensity at different concentrations of L-Pro in DMSO. The reaction rate constants (k) were calculated based on first-order kinetics (equation (1)) (Figure 2(b)), suggesting that the reaction could proceed by following first-order kinetics, because the reaction rate and amount of L-Pro (catalyst) were almost in a linear relationship at L-Pro concentrations below 40 μM.

(a)

(b)

To investigate the effect of solvent polarity, the reaction was further conducted in the system of DMSO/water mixture. Figure 3 shows the time course of the fluorescence intensities, wherein the fluorescence intensities were monitored at 362 nm. The presence of water significantly decreased the reaction rate. In general, the enamine formation can be inhibited by the solvent water [4]. It is suggested that water molecules also play an inhibitory role in this reaction. Common to the reaction mechanisms of the L-Pro-catalyzed reactions, the formation of the enamine intermediate is the key to achieve efficiency and enantioselectivity [2, 3, 15], whereby the water molecules could decrease the stability of the enamine intermediate. During the formation of the enamine of L-Pro and acetone, unstable intermediates can be formed [16]. When the reaction is carried out in liposome membranes, such intermediates could be stabilized by interaction with phospholipid molecules [11]. These results clearly indicate that the efficiency of the L-Pro-catalyzed reaction of BIPM and acetone can be inhibited in an aqueous solution, owing to the lack of hydrophobic (dehydrated) environment. The reactions catalyzed by D-Proline (D-Pro) were also investigated, but the catalytic activity of D-Pro might be lower than that of L-Pro (Figure 3). In most cases, L-Pro and D-Pro show similar catalytic performances except for the enantioselectivity of the product [17]. However, in some examples, the yield of the product differed depending on the proline structure [18]. In the case of direct asymmetric aldol reaction between p-nitrobenzaldehyde (pNBA) and acetone, the D-Pro derivative drastically decreased the reaction yield [2]. The carboxyl group of L-Pro also produced a good yield [2]. It is assumed that L-Pro can improve the reactivity of the enamine intermediate, suggesting that the enamine composed by L-Pro (or its derivatives) shows higher reactivity as compared to D-Pro derivatives, but further determinations are needed to investigate their differences. In addition, as D-Pro is hardly adsorbed onto liposomes [13], it was difficult to perform the D-Pro-catalyzed reactions at the liposome membrane. In this study, the L-Pro-catalyzed Michael addition reactions of BIPM and acetone are further investigated in the following sections.

3.2. Coexistence Effect of Liposome Membrane L-Pro-Catalyzed Reaction in an Aqueous Solution

The coexistence effect of the liposome membrane on the L-Pro-catalyzed reaction of BIPM and acetone was investigated in water. Although L-Pro is a water-soluble molecule, it has been reported that L-Pro can be adsorbed onto the liposome surface by incubation for 48 hours [13]. After L-Pro was preincubated with the DPPC liposome for 24 or 48 hours, the Michael addition reaction was initiated by adding BIPM and acetone. Figure 4(a) shows the fluorescence spectra of the products at different incubation times. In the case of 24-hour preincubation, the spectra were not changed significantly, indicating that the reaction did not proceed. On the contrary, after 48-hour preincubation, the fluorescence intensities were drastically increased, showing that the L-Pro-catalyzed reaction of BIPM and acetone was achieved in the aqueous medium when the liposome was coexisting. The adsorption amounts of L-Pro onto liposomes were approximately 10% of the total L-Pro—8.3% for the DOPC liposome, 10.8% for the DPPC liposome, and 11.4% for the DPPC/DPTAP liposome, at 48-hour incubation. We assume that only the adsorbed L-Pro possesses high catalytic activity, whereas the unadsorbed L-Pro can behave as free L-Pro. Although we have not estimated the L-Pro adsorption amount at 24 hours, in almost all cases, the adsorption amount at 24 hours is less than 20% of the maximum adsorption amount (at 48 hours). Considering these results and findings, the adsorption amounts of L-Pro could be estimated as <100 μM for 48 hour preincubation and <20 μM for 24-hour preincubation. This could be the reason why the reaction rate constants in liposome systems turn out to be lower than those in the DMSO solvent.

(a)

(b)

Figure 4(b) shows the time course of the fluorescence intensity, showing that the k value at 48-hour preincubation was five times higher than that of 24 hour preincubation. It has been reported that the L-amino acid adsorption did not proceed until 24 hours and then dramatically proceeded within 24- to 48 hour preincubation [13], in which the liposome surface properties could be varied by the adsorption of L-amino acids and then concerted binding could be initiated. The obtained results show that the Michael addition reaction of BIPM and acetone was promoted by the L-Pro that was adsorbed onto the membrane surface. Considering the facts that (1) water molecules principally inhibit the L-Pro-catalyzed reaction and (2) the liposome membrane provides a hydrophobic environment in the aqueous medium, the L-Pro-catalyzed reactions can be carried out in an aqueous medium, owing to the presence of the liposome membranes. The potential roles of the liposome membrane are to carry the hydrophobic reactant (BIPM) in the interior region of the membrane and to accumulate reactants and a catalyst in the dehydrated environment.

3.3. Effect of Type of Liposome Membrane on the L-Pro-Catalyzed Reaction

Biological membranes consist of various kinds of lipids and proteins. Among the naturally occurring zwitterionic phospholipids, DOPC and 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) were selected to investigate the effect of membrane properties on this reaction. At room temperature, DOPC and DPPC liposomes are in the fluid state (liquid-disordered, L_d, phase) and rigid state (solid-ordered, s_o, phase), respectively. It is also reported that the cationic liposome DPPC/DPTAP (1,2-dipalmitoyl-3-trimethylammonium-propane) can improve the L-Pro-catalyzed Michael addition reaction [9]. After L-Pro preincubation for 48 hours, the reaction of BIPM and acetone was carried out in the presence of the abovementioned liposomes (Figure 5). The initial reaction rate was herein analyzed by the slope of the approximately straight line of the plot of fluorescence intensity at 372 nm against time, as the fluorescence intensity increased proportionally with time. The initial reaction rate in DPPC (s_o phase) was 2.5 times higher than that in DOPC (L_d phase). Furthermore, the addition of cationic DPTAP decreased the initial reaction rate, although both the DPPC and DPPC/DPTAP liposomes are in rigid membrane states (s_o phases) [9].

The membrane surface of the DPPC liposome is known to be in a dehydrated state as compared to that of the DOPC membrane [9], which could be favorable to stabilize the enamine intermediate of L-Pro and acetone. In addition, the “ordered” state of the DPPC membrane could contribute to promote the adsorption of the L-amino acid (including L-Pro), whereas L-amino acid adsorption can decrease when the membrane is in disordered states [13]. The adsorption of L-Pro was slightly increased by the positively charged liposomes [9], whereas the membrane property differences between DPPC and DPPC/DPTAP could be negligible. Thus, the inhibitory effect of the DPTAP on the reaction could be because of the positive charge of the membrane. Furthermore, only the positively charged molecules (e.g., propranolol) adsorbed onto the negatively charged liposomes [19]. It is assumed that L-Pro could preferentially adsorb onto the membrane in the s_o phase, in which the less hydrophobic environment contributes both to the adsorption of L-Pro and to the promotion of the Michael addition reaction.

3.4. Plausible Model of L-Pro-Catalyzed Michael Addition Reaction of BIPM and Acetone in Liposome Membrane

Based on the abovementioned results, a plausible model of the L-Pro-catalyzed Michael addition reaction is discussed. To assess the location of the product in the liposome membrane, the peak shift of the emission fluorescence of the reaction product was analyzed in various kinds of solvents with different polarities. In the existing literature, it has been reported that the fluorescence intensity of the product in DMSO was slightly higher (∼1.6 times) than that in water [14]. To verify the solvatochromism of the product, the product recovered in DMSO solvents after 24 hour incubation was transferred into DMSO/water mixtures for further analysis of its fluorescence. Figure 6(a) shows the emission peak wavelength of the reaction product in both 1,4-dioxane/water systems and DMSO/water systems. The emission peaks gradually red-shifted as the water ratio increased. In the liposome systems, the emission peaks were observed at 368.5 nm (we confirmed the emission peaks with three isolated data from DOPC and DPPC). This suggests that the products generated in the liposome tend to locate at the hydrophilic part (near the lipid head groups) although the emission peaks were broader in the liposome systems. The emission peak intensities were decreased in proportion to the water ratio (Figure 6(b)). The fluorescence intensity of the product in water decreased to 40%. In contrast, the presence of water in the reaction mixture drastically inhibited the reaction (Figure 3), suggesting that the formation of the enamine intermediate of L-Pro and acetone could be the key to promote this reaction. The DMSO environment is suitable to stabilize enamine [2, 3], and a similar effect can be obtained by utilizing the liposome membrane [9, 11].

(a)

(b)

The possible locations of the molecules related to this reaction are summarized in Figure 7. L-Pro, the enamine intermediate, and acetone could be basically localized at the interface region, near the phosphate and glycerol groups; therefore, the enamine intermediate could be stably trapped there. The reaction could be completed by the attack of the enamine intermediate to BIPM, which could be located in a more hydrophobic region—near the hydrocarbon chains of lipids. Similarly, the reactants trans-β-nitrostyrene (tβNS) and pNBA can be estimated to be located at the hydrophobic site [9, 11]. The obtained results and previous findings suggest that the enamine intermediate, composed of L-Pro and acetone, could preferentially locate in the hydrophobic region of the liposome membrane, which successfully promotes the L-Pro-catalyzed reactions. The efficiency and enantioselectivity can be varied, preferably depending on the property of the reactant—tβNS would provide high enantioselectivity; pNBA would provide high conversion but low enantioselectivity. For BIPM, although the conversion was lower, the reaction kinetics was directly analyzed in the aqueous medium, revealing that the L-Pro-catalyzed Michael addition of BIPM and acetone was surely performed in the liposomal membrane.

4. Conclusions

The kinetics of the L-Pro-catalyzed Michael addition reaction of BIPM and acetone were analyzed by using fluorescence spectroscopy. The composition of liposomes could be a controlling factor in this reaction—the zwitterionic DPPC liposome displayed the highest reaction rate constant among the liposomes tested in this work. From the point of view of green chemistry, organic synthesis in aqueous media provides various benefits. On the contrary, in food science and engineering fields, our findings provide a warning that the L-Pro distributed into biomembranes (hydrophobic environment) can react with ketones, which might lead to unexpected and inconvenient chemical reactions in the human body. The ketones can be produced by lipid oxidation in biomembranes; thus, ketones in biomembranes would be reactive in the presence of L-Pro, which might result in unexpected products. Thus, in situ detection of the L-Pro-catalyzed reactions is necessary. The obtained results provide us with an easily detectable method to assess the risk of L-Pro in biological systems, which can be detected using BIPM as a donor reactant in the L-Pro-catalyzed Michael addition reaction.

Abbreviations

L-Pro:	L-Proline
DMSO:	Dimethyl sulfoxide
BIPM:	N-[p(2-Benzimidazolyl)phenyl]maleimide
DPPC:	1,2-Dipalmitoyl-sn-glycero-3-phosphocholine
DOPC:	1,2-Dioleoyl-sn-glycero-3-phosphocholine
DPTAP:	1,2-Dipalmitoyl-3-trimethylammonium-propane
T_m:	Phase transition temperature
MLV:	Multilamellar vesicle
LUV:	Large unilamellar vesicle
CH₃CN:	Acetonitrile
D-Pro:	D-Proline
pNBA:	p-Nitrobenzaldehyde
L_d:	Liquid disordered
s_o:	Solid ordered
tβNS:	trans-β-Nitrostyrene.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Acknowledgments

This work was supported by the JSPS Grant-in-Aid for Scientific Research A (26249116), Challenging Exploratory Research (T15K142040), and Sasakawa Scientific Research Grant from the Japan Science Society (29-336). We thank Dr. Takaaki Ishigami and Dr. Yukihiro Okamoto (Graduate School of Engineering Science, Osaka University) for their constructive comments and technical support.

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Copyright © 2019 Masanori Hirose et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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