We investigate the influences of the excluded volume of molecules on biochemical reaction processes on 2-dimensional surfaces using a model of signal transduction processes on biomembranes. We perform simulations of the 2-dimensional cell-based model, which describes the reactions and diffusion of the receptors, signaling proteins, target proteins, and crowders on the cell membrane. The signaling proteins are activated by receptors, and these activated signaling proteins activate target proteins that bind autonomously from the cytoplasm to the membrane, and unbind from the membrane if activated. If the target proteins bind frequently, the volume fraction of molecules on the membrane becomes so large that the excluded volume of the molecules for the reaction and diffusion dynamics cannot be negligible. We find that such excluded volume effects of the molecules induce non-trivial variations of the signal flow, defined as the activation frequency of target proteins, as follows. With an increase in the binding rate of target proteins, the signal flow varies by monotonically increasing; increasing then decreasing in a bell-shaped curve; or increasing, decreasing, then increasing in an S-shaped curve. We further demonstrate that the excluded volume of molecules influences the hierarchical molecular distributions throughout the reaction processes. In particular, when the system exhibits a large signal flow, the signaling proteins tend to surround the receptors to form receptor-signaling protein clusters, and the target proteins tend to become distributed around such clusters. To explain these phenomena, we analyze the stochastic model of the local motions of molecules around the receptor.
Citation: Fujii M, Nishimori H, Awazu A (2013) Influences of Excluded Volume of Molecules on Signaling Processes on the Biomembrane. PLoS ONE 8(5): e62218. https://doi.org/10.1371/journal.pone.0062218
Editor: Johannes Reisert, Monell Chemical Senses Center, United States of America
Received: October 31, 2012; Accepted: March 18, 2013; Published: May 2, 2013
Copyright: © 2013 Fujii et al. 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.
Funding: This work was supported by the Research Fellowship of the Japan Society for the Promotion of Science for Young Scientists to MF (www.jsps.go.jp), by the Global Center of Excellence Program G14 (Formation and Development of Mathematical Sciences Based on Modeling and Analysis) of Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan to HN (www.jsps.go.jp), and by the Grant-in-Aid for Scientific Research on Innovative Areas (Spying minority in biological phenomena (No. 3306) (24115515)) of MEXT of Japan to AA (www.jsps.go.jp). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Several living systems can sense and respond to environmental variations by means of internal biochemical processes. The adaptation of cells and the cell fate determinations in multicellular organisms (e.g., cell proliferation, differentiation, and apoptosis) are typical behaviors regulated by intracellular signal transduction processes –. These simultaneous internal biochemical processes require the synthesis and interaction of a number of different proteins on various biomembranes and in the cytoplasm involving several macromolecules, the cytoskeleton, and organelles.
Recent studies suggest that the volume fraction of macromolecules in individual cells is much higher than that under typical in vitro conditions –. The total volume concentration of macromolecules in a typical cell is estimated to be 50–400 , whereas under typical in vitro conditions, it is estimated as 1–10 . Such a high volume fraction of molecules, commonly called “molecular crowding'', gives rise to extreme spatial restrictions. Thus, the diffusion and deformation (reaction) of molecules in the cytoplasm are highly suppressed –. Such spatial restrictions are also expected to enhance protein folding , , protein formation, stabilization of the intracellular architecture , and processive phosphorylation of ERK MAP kinase , .
The transduction of signals from the extracellular environment starts with the activation of receptors and signaling proteins on the cell membrane. Thus, the sensing and response of cells are dependent on the effective transport and reaction of signaling proteins in a 2-dimensional space. Recently, imaging measurements of macromolecules on the cell membrane have been performed extensively –. In some of these measurements, the typical motion of membrane proteins was revealed to be subdiffusive –. This observation implies the existence of intrinsic membrane domains, such as raft or nonimaged molecules, which restrict the observed molecular motions by means of their excluded volumes. Thus, to better understand the performance and mechanisms of the upstream part of the signal transduction processes, the excluded volume effects of molecules on the reaction and diffusion dynamics of 2-dimensional systems should be clarified.
In this paper, we investigated the influences of the excluded volume of molecules on biochemical processes using a simple model of typical signal transduction processes on the biomembrane. In the next section, we provide a brief introduction of G protein-coupled receptor (GPCR) signaling processes as a typical signal transduction process on the cell membrane and construct a model inspired by these processes. In the third section, we perform the simulation of the model and the analysis of a more simplified model. The summary and conclusion are presented in the final section.
Model and Simulation Method
Typical signal transduction processes on the biomembrane
In this section, we introduce a simple model of biochemical reaction processes that mimics the GPCR signaling processes on the biomembrane. GPCR signaling processes are typical signaling processes that play important roles in adaptations to environmental variations. The followings is a brief introduction to these processes.
G proteins and GPCRs constitute large protein families of guanine nucleotide-binding proteins and their receptors , . GPCRs sense extracellular signals (light-sensitive compounds, odors, pheromones, hormones, and neurotransmitters). The GPCRs activated by the extracellular signals activate G proteins by exchanging GTP in place of the GDP on G proteins. The activated G proteins usually separate into the subunit (-) and complex (). Both - and activate different second messenger or effector proteins. The second messengers of some signaling pathways are located on the membrane and unbind from the membrane following activation in order to transfer the signals downstream of the signaling pathway to genes through lower hierarchical signal transductions. The GTP binding to is hydrolyzed and becomes GDP, and then - binds to . The inactivated G protein, i.e., --binding , can rebind to the GPCR.
The abovementioned signaling processes can be summarized as the following: The signaling proteins (G protein) activated by the receptor (GPCR) activate the target proteins (second messengers) on the membrane. The activated target proteins unbind from the membrane to transfer the signal downstream of the signaling pathways. A similar reaction cascade is also involved in the EGF-RAS-RAF signaling process on the membrane –. Based on these facts, we constructed a simple model of the membrane signal transduction processes containing only typical molecular processes, as described in the next subsection.
Reaction scheme of the model
The model consisted of active and inactive receptors ( and ), active and inactive signaling proteins ( and ), bound and unbound target proteins ( and ), and nonreactive molecules (crowder, ), which diffuse and react in a 2-dimensional space. Here, each molecule, , , , , , and , possessed its own volume. These molecules moved randomly under the restriction of their excluded volumes. Specifically, the distance between the centers of 2 molecules could not be smaller than the sum of their radii of inertia.
The signal transduction process is described as a cascade that follows the activation of receptors to the unbinding of activated target proteins from the membrane through the following reactions (Figure 1).
(1) The extracellular signal is transferred via activation of the receptor (Equation [Eq.] 1). (2) Autonomous inactivation of the receptor (Eq. 2). (3) Activation of the signaling protein by the active receptor (Eq. 3). (4) Autonomous inactivation of the signaling protein (Eq. 4). (5) Stochastic binding of the target protein from the cytoplasm to the membrane (Eq. 5). (6) Activation and unbinding of target proteins by active signaling proteins (Eq. 6). (7) Autonomous unbinding of the target protein (Eq. 7).
- A receptor autonomously changes from active to inactive, and vice versa, with the reaction rates and , respectively, described by (1)and(2)
- When an inactive signaling protein makes contact with an active receptor, this signaling protein is activated with the reaction rate . The active signaling protein autonomously becomes inactive with the reaction rate . These processes are described by (3)and(4)
- If an empty space exists on the membrane, a target protein autonomously binds there with the rate . When a target protein makes contact with an active signaling protein, this target protein is activated with reaction rate . The target protein unbinds from the membrane as soon as it is activated. In the absence of activation, the target protein autonomously unbinds from the membrane with the reaction rate . These processes are described by (5)(6) and(7)
is proportional to the rate of target protein binding to lipids in the membrane when they collide with each other. This rate in termed. denotes the affinity between a target protein and the membrane. Moreover, is proportional to the number density and the diffusion rate of the target protein in the cytoplasm. Thus, indicates the effective binding rate of the target protein, which depends on the molecular species and cell species, and cell conditions. We assume that varies in the range of 0–1, where indicates that the is large enough and/or that the number density of target proteins in the cytoplasm is high enough. We have also noted that the diffusions of molecules in the cytoplasm are much faster than those on the membrane. Subsequently, the target proteins in the cytoplasm tend to distribute uniformly and collide frequently with the membrane. Thus, in this model, we assumed that is uniform in space.
We have used a 2-dimensional cell-based model ,  to describe the diffusion and reactions of active and inactive receptors ( and ), active and inactive signaling proteins ( and ), target proteins (), and crowders () on the membrane. The space was divided into 2-dimensional hexagonal cells as shown in Figure 2. We defined the boundary condition of the system as periodic. Each cell could contain only one molecule, which represented the excluded volume effect. Each molecule randomly hopped from one cell to a neighboring empty cell or reacted in the manner indicated by Equations 1, 2, 4, 5, or 7. Reactions 1, 2, 4, and 7 occurred spontaneously with the given reaction rates, whereas 2-body reactions 3 and 6 occurred when 2 corresponding molecules existd in adjacent cells. No reaction occurred by the crowders. In the empty cells, reaction 5 occurred at the rate .
To simulate the present cell-based model, we used the Monte-Carlo method. The temporal evolution of the system progressed by the iteration of the following steps.
and are distributed randomly to yield the initial condition.
One of the cells is chosen randomly.
If this cell contains molecule or , the corresponding 2-body reactions, 3 or 6, occur at a rate determined by the product of its given [reaction rates] [the number density of the corresponding catalyst on the six neighboring cells]. is removed from this cell as soon as it appears.
If this cell contains molecule , , , or , the corresponding reaction, 1, 2, 4, or 7, occurs with its respective reaction rate. Reaction 7 indicates that is removed from this cell.
If this cell contains a molecule but no reaction occurs, this molecule moves randomly to one of the 6 neighboring cells as long as the chosen cell is empty.
If this cell contains no molecule, the binding process of a target protein 5 occurs with the reaction rate . This indicates that becomes bound to this cell with the reaction rate .
In each time step, – are iterated times, where is the number of cells. We defined the time step of the system as when – were iterated times from the initial condition. In this study, we assumed the length of each cell was , and order of unit time step was (details are provided in Text S2).
We definde the signal flow, , as the average frequency of target proteins per receptor. at time is derived from [Number of activations of target proteins between and +1]/[Number of receptors]. We also defined the “occupancy'' of molecules as [Total number of molecules in the system]/, and the occupancy of molecule as . In the cell-based model, this value was used as an index of the crowding of molecules instead of the volume fraction of molecules frequently measured in experiments. It was assumed that the volume fraction of molecules in the system and their occupancy in the corresponding cell-based model were positively correlated. The rough estimations of the volume fractions of molecules from the occupancy in simple molecular systems are stated in Text S2.
Recently, there have been few experimental observations of the total volume fractions of molecules on cell membranes. However, such aspects are naturally expected to depend on the specificity of molecules around the membrane and on cellular conditions. In the present model, the effects of such specificities are described by the parameters and , and the occupancy of signaling proteins remaining on the membrane. Thus, in the present study, we systematically varied these parameters in order to consider the possible reaction behaviors on a biomembrane in several possible situations.
Results and Discussion
In this section, we consider the typical properties obtained through the simulation of the model, which did not include crowders. We focus on the steady-state signal flow , defined as the average frequency of the target proteins activations per receptor, and the total occupancy of molecules, , for several values of signaling protein occupancy, , the effective binding rate of the target protein, , and autonomous unbinding rate of the target protein, . For simplicity, some parameters were fixed: , , , , and . Here, and indicate that all receptors are always activated. The qualitative results are unaffected by these parameters if is large enough and is small enough, i.e. signals are input frequently from outside the cell. We also assumed that the occupancy of the receptor was a low value, , as recent experimental observations have reported that the volume fraction of receptors on the cell membranes is estimated as a few percent –. However, the following arguments are qualitatively independent of these details.
Here, the derivation of this form is provided in Text S1. This result indicates that is a monotonically increasing function of that takes place in the form of a Michaelis-Menten-type equation independent of the values of the reaction rates, , and . On the other hand, the simulations results of the presented model deviate considerably from those expected by mean-field analysis, as described below.
Figure 3A and 3B depict and as functions of obtained by the simulation for the parameter sets (red plus), (green cross), and (blue circle). As shown in Figure 3, unlike the result obtained by the mean-field analysis, there are 3 typical variations with the increase in , increasing monotonically, increasing then decreasing in a bell-shaped curve, and increasing, decreasing, then increasing in an S-shaped curve. Figure 4 illustrates the phase diagram of the – relationship at each and . Here, exhibits a monotonic increase for a case of large , a bell-shaped curve when both the and are small, and an S-shaped curve for the case of a large and small .
(A) Signal flow and (B) total occupancy as functions of the binding rate of the target protein for as functions of the binding rate of the target protein (red plus), (green cross), (blue circle) obtained by simulations, and that for obtained by the mean field analysis (black line).
The finding in the previous subsection implies the existence of a spatially nonuniform distribution of molecular species. Thus, to observe the characteristic spatial distributions of molecules, we measured the radial distribution function of each molecular species around each receptor. The radial distribution functions of the signaling proteins and target proteins around the receptor, , and , are defined as(9)(10) respectively. Here, indicates the local occupancy of molecule at a distance from the receptor (seef Text S3). Donates the sample and long time-averaged value. Molecule is considered dense when , and sparse when , compared to the uniform distribution.
Figure 5 depicts typical snapshots of the simulation and radial distributions of the signaling protein (green cross), and the target protein (blue circle) for the following cases: (A) at which realizes the largest value in the case that monotonically increases with , (B) at which decreases along the bell-shaped curve, and (C) at which yields a local minimum of the S-shaped curve. It should be noted that snapshots and radial distributions similar to Figure 5A can be obtained for parameter sets in which is at the peak of the bell-shaped or S-shaped curve. In these cases, the molecules tend to distribute according to the following spatial structure: the signaling proteins surround the receptor to form the receptor-signaling protein cluster (- cluster), and the target proteins become distributed around such clusters. If the molecular distribution occurs according to the abovementioned structure, around and around tends to be activated rapidly. Subsequently, the reaction process of the system progresses actively.
(A) , (B) , (C) . Each black, orange, and blue point indicates a receptor, signaling protein, and target protein, respectively.
The qualitative mechanism of the formation of - clusters is explained as follows. Around , is frequently activated to , and near is also frequently activated. The activated unbinds from the membrane. Then, empty spaces appear around , i.e., near . These empty spaces are occupied by other molecules according to the diffusion or binding of . Through these processes, the molecular flow in which molecules approach tends to be formed. At the terminal of this molecular flow, tends to unbind by the activation, but () remains near . Thus, - clusters are formed.
In the case of appropriate values of and , in which is not as large as compared to , is distributed around the - clusters. However, other types of molecular distribution often appear, in particular, in the case of a small . For example, in the case of a large and small , in which is much smaller than , tends to be surrounded not by but , as in Figure 5B. On the other hand, in the case of a large , the - cluster tends to be surrounded by , as in Figure 5C.
Now, we explain the behaviors of the present model qualitatively, based on the abovementioned molecular distributions. First, we considered the case of a small and small . If the is too small, where the total occupancy of molecules is so small that the excluded volume effects can be neglected, increases with , as considered in the mean-field analysis. Moreover, in the case of a not-so-large , appears an appropriate values compared to ; increases with because - clusters appear and the surrounding them increases. However, with the increase in , becomes so much larger than that tends to surround between instead of . Thus, increases then decreases in a bell-shaped curve with the increase in . On the other hand, if the is large enough, an - cluster can be formed even in the case of a large because around often unbinds and can approach to surround them.
Next, we considered the case of a small and large . Similar to the above case, if the is small enough, increases with . On the other hand, with the increase in the total occupancy of molecules by the increase in , - clusters surrounded by appear. Here, around the - clusters is usually inactive because it cannot be activated by . If is not so large that the total occupancy of molecules is not large either, can surround the - cluster and can exchange their positions by their diffusion. Then, can be activated and increases with . On the other hand, such diffusions and exchanges tend to be suppressed with the increase in . Then, decreases with the increase in in a range of not-small-enough . However, for a much larger , can invade the void between the - cluster and around the cluster by binding from the cytoplasm and being activated as soon as such a void appears. Here, such voids are created by the fluctuation of the reaction and diffusion of molecules on the membrane. If the is large enough, around the - cluster and can exchange positions smoothly even in the case of a large because near around the - cluster often unbinds, and can diffuse. Then, often approach - clusters and always increases with .
The above qualitative considerations are consistent with the mathematical analysis of the present model through the more simplified model, as mentioned in the next subsection. In the present argument, we assume that the signaling protein cannot unbind from the membrane. However, the qualitative results are unchanged even when the signaling proteins can autonomously unbind from the membrane if the unbinding rate of the signaling proteins is small enough compared to that of the target proteins.
Theoretical analysis by a simple stochastic model
The results of the previous subsection indicate that the structure of the molecular distribution around the receptor forms a dominant contribution to the reaction activity of the present system. In this subsection, we analyze a simple 1-dimensional stochastic model that describes the molecular motions in the radial direction around a receptor. The analysis is then compared to 3 described – relationships. For simplicity, we consider the case that only one receptor exists in the system and is always activated, i.e. .
We consider the following 3 typical states of the molecular distributions in the radial direction around a receptor as: “'', where no molecule exists beside the receptor; “'', where the target protein exists beside the receptor; and the state where the signaling protein exists beside the receptor and is activated. The third state is divided into the following 2 states: “'', where no molecule exists beside the active signaling protein, and “'', where an inactive signaling protein exists beside the active signaling protein. Here, in the states “'', “'', and “'', any reactions can not occur. On the other hand, in the “'' state, the reaction occurs if a target protein appears beside . Note that other states exist, such as “'', “'' and “''. To simplify, however, we have omitted these states from this analysis by considering the following assumptions. The target protein beside is rapidly activated and unbound. The signaling protein becomes inactive immediately if it leaves the receptor. The signaling protein is activated as soon as it approaches next to the receptor.
Moreover, we assumed that the molecular distributions around a receptor are almost uniform in terms of the angle direction as shown in Figure 6, which is roughly supported by the simulation results in the previous subsections. Then, we only considered the molecule reactions and diffusions only in the radial direction. Although these assumptions render the model too simple, the appearance of the 3 types of – relationships obtained in the previous subsection can be explained qualitatively as follows.
, the receptor; , inactive signaling protein; , active signaling protein; and , target protein; each denotes , , , , or empty.
Now, we consider the following transition dynamics among these 4 states,(11)where , , , , , and indicate the transition rates. These transition rates are approximately estimated by , , , and as follows.
: The transition from “'' to “'' indicates that diffuses away from beside . The transition rate is proportional to the probability that any molecules do not exist beside . Then,(12)where indicates the diffusivity of molecules.
: The transition from “'' to “'' indicates that diffuses from an adjacent space to occupy the empty space beside . This transition rate is proportional to the probability that no appears, but does. The probability of the appearance of is estimated as , and that of is estimated as , which is the sum of contributions by the binding from the cytoplasm and the diffusion of target proteins on the membrane. Then,(13)
: The transition from “'' to “'' indicates that leaves from beside before any molecules occupy the empty space beside . The probability that 1 molecule ( or ) appears at the empty space beside is estimated by . Then,(14)
: The transition from “'' to “'' indicates that diffuses from an adjacent space to occupy the empty space beside . The properties of this transition are almost the same as those of “'' to “''. Then,(15)
: The transition from “'' to “'' indicates that originates from the cytoplasm or adjacent spaces on the membrane to occupy the empty space beside . This transition rate is proportional to the probability that no appears but does. Then,(16)
: The transition from “'' to “'' indicates that leaves from beside . This transition rate is yielded by the sum of 2 contributions: the autonomous unbinding from the membrane and the diffusion of . The diffusion of is proportional to the probability that any molecules do not exist beside . Then,(17)
Here, it should be noted that while and and are the control parameters of the present system, should be derived from these parameters. In the following analysis, with reference to the simulation results in Figure 3B, we assume is derived as(18)with the fitting parameter .
The steady-state signal flow is estimated by [the probability of appearance of the target protein beside ]. The latter probability is that for which no appears but does, by diffusion or binding from the cytoplasm. Then, .
Figure 7 depicts (A) as a function of for some parameter sets of , and (B) the phase diagram of – relationships against , and for , obtained by analyzing the steady state solutions of the present stochastic model. These results are qualitatively independent of . As shown in these figures, we obtained results that were qualitatively similar to the simulation results in the previous subsections.
(A) Signal flow as a function of for ( (red plus), (green cross), and (blue circle); (B) phase diagram of -- relation for each and . Each symbol is plotted in the same manner as Figure 4.
Then, we considered the detailed properties of this model. It should be noted that is also described as(23)which indicates that depends on the ratios between the transition rates, , , , and . Then, the appearances of the 3 types of - dependency can be explained by considering the dependencies of , , and as follows.
Figure 8 illustrates (A) , (B) , (C) and (D) as functions of for combinations of and , where their analytic forms are obtained by
(24)(25)(26)and Equation (16). Figure 8B and 8C and Equations (25) and (26) indicate that is a monotonically decreasing function of and a monotonically increasing function of , and that is almost proportional to and a monotonically decreasing function of . This indicates that, with the increase in , tends to make contact with other molecules because the occupancy, i.e., the volume fraction, of molecules on the membrane increases. In the same manner, increases monotonically with as indicated in Figure 8D and Equation (16). However, the slope of each curve varies from steep to gradual because increases with but is saturated for a large .
On the other hand, as shown in Figure 8A, the variations of are somewhat more complicated, as follows. Equation (24) indicates that has a maximum at(27)for a large and small that satisfies. On the other hand, with an increase in , decreases monotonically for . Furthermore, it increases with the increase in . The appearance of this maximum of for a small means that with the increase in , the “'' state tends to occur for a small or intermediate value of , but the transition rate to the “'' state tends to be hindered for a large . The reason for this is considered to be as follows. With the increase in the , the occupancy of molecules becomes large. Then, the molecules tend to make more contact with each other, inducing the transition from “'' to “''. On the other hand, if becomes much larger, can approach beside more frequently (and is activated and unbinds immediately) by the binding from the cytoplasm before diffuses close to . With the increase in , then increases for a not-so-large , but decreases for a large .
According to the abovementioned dependencies of each term, the appearances of the 3 - relationships are explained as follows:
For a large , and are monotonically decreasing functions of . Even if we assume that and are constant values, is given as a monotonically increasing function of in the form of a Michaelis-Menten-type equation. According to these facts, increases monotonically with .
For a small and small , is sufficiently larger than and for a small . Then, only is the dominant term of the denominator of Equation (23). In this case, the denominator of Equation (23) is considered constant. Then, increases with for a small , since monotonically increases with . On the other hand, increases with , and finally exceeds . Then, also becomes the dominant term of the denominator of Equation (23). Here, the slope of becomes gradual with the increase in , while the slope of is unchanged and is regarded as constant for a large . Therefore, decreases with the increase in for a large . exhibits the bell-shaped curve.
For a small but large , becomes dominant as compared to and for a small . Here, is approximately constant for a small . Then, the dominator of Equation (23) is considered constant. On the other hand, increases to the same order as that of with the increase in . Then, also becomes the dominant term of the denominator of Equation (23). Thus, in a similar manner to case , increases and turns to decrease with . However, if approaches 1, exhibits a drastic decrease where the slope of the decrease in is much steeper than that of the increase in . Then, the denominator turns to decrease in the neighborhood of , and increases again with .
Furthermore, the at which exhibits a maximum peak is obtained by the intersection of and , i.e., . Thus, the that exhibits the peak shifts to the larger value with the increase in . On the other hand, the at which exhibits the local minimum of the S-shaped curve slightly decreases with the increase in . Here, the local minimum value of increases with the increase in . If increases more, the local minimum of vanishes as shown in Figure 9.
Reaction system with crowding molecules
In the previous subsections, we considered a simple model of an ideal situation that was assumed to comprise only the components of the signal transduction processes. However, in general, several reaction processes take place simultaneously on the cell membrane, using several macromolecules. The components of these other reactions often behave as obstacles for the components of other reaction processes. Thus, to elucidate the influences of the excluded volume of molecules using a more realistic model, we simulated a system containing a crowder molecule, . Here, moved randomly on the membrane without reaction, binding, or unbinding. It only hindered the random movements of other reactive molecules because of its excluded volume.
Figure 10 depict the - relation for (A) , (B) and (C) with , described in the same manner as Figure 4, (D) a typical snapshot of the simulation, and (E) the radial distributions of the signaling proteins , the target proteins , and the crowder for , , , and , described in the same manner as Figure 5. As shown in Figure 10A and 10B, the phase diagrams for not too many large values of are qualitatively the same as those obtained when (no crowders). We also observed that the signaling proteins tended to distribute around the receptor on average, as shown in Figure 10D and 10E, when the system exhibited a large , similar to the - cluster formation observed in the case of .
(D) Typical snapshot of the simulation, (E) radial distributions of signaling proteins (green cross), target proteins (blue circle), and crowder (yellow triangle) plotted as a function of the distance from a receptor for , , , and , which are plotted in the same manner as in Figure 5. Each black, orange, blue, and gray point indicates a receptor, signaling protein, target protein, and crowder, respectively.
However, in the phase diagrams, the phase boundary between the regions with bell-shaped and S-shaped – relations shifted to a large with an increase in . Moreover, in cases of a much larger , such as , the region with the S-shaped relation disappeared, as shown in Figure 10C. The reason for these facts is believed to be as follows. The appearance of the S-shaped relation was caused by the aggregation of to form the - cluster surrounded by , as mentioned in the previous subsections. However, with the increase in , such aggregations of tended to be hindered and required more to be formed. Thus, the phase boundary between the regions with bell-shaped and S-shaped - relations shifted to a large . Moreover, if became much larger, could not be so large as to form such aggregations of . Hence, the region with the S-shaped relations disappeared.
Summary and Conclusion
We investigated the influences of the excluded volume of molecules on the activity of reaction processes on 2-dimensional surfaces using a cell-based model of signal transduction processes on biomembranes. The simulation was based on the diffusion and reaction among receptors, signaling proteins, target proteins, and crowders on a 2-dimensional surface.
With the increase in the binding frequency of target proteins to the membrane, the volume fraction of molecules on the membrane increased in a similar manner to the molecular crowding in the cytoplasm. However, the reaction behaviors on such a 2-dimensional membrane were obtained differently from those in a 3-dimensional bulk system. We found that the signal flow exhibited 3 types of molecular volume fraction dependencies according to the abundance ratio and the binding/unbinding rate of the molecules constructing the system: When the autonomous unbinding of target proteins occurred frequently, the signal flow increased monotonically with the binding rate of the target proteins. When the autonomous unbinding of target proteins occurred rarely and the number of signaling proteins was small, the signal flow increased for the small values of the binding rate, and then decreased for the large value of the binding rate of the target proteins. When the autonomous unbinding of target proteins occurred rarely and the number of signaling proteins was sufficiently large, the signal flow increased and decreased as in , but then increased again for a sufficiently large value of the binding rate of the target proteins. We further demonstrated that the excluded volume of molecules influenced their hierarchical distributions throughout the reaction processes. In particular, when the system exhibited a large signal flow, the signaling proteins tended to surround the receptors and the target proteins tended to distribute around the receptor–signaling protein clusters, which accelerated the activations of the signaling proteins and target proteins.
To control the signal transduction activity on the membrane, we expect that the formation of the presented hierarchical molecular distributions makes a dominant contribution along with receptor clustering . On the other hand, a large number of reaction processes other than the signaling cascade are known to take place on the interior and exterior surfaces of several biomembranes of organelles, such as the mitochondria, Golgi body, and nucleus. The molecular distributions on the majority of such membranes are not clearly understood experimentally, except the recent reports of the aggregations of peptides related to some diseases , , . Such studies are progressing as ongoing issues or will be studied as future issues. For such problems, based on our present argument and extended arguments with more realistic models, we predict that several molecule aggregation patterns are formed by the excluded volume of molecules and influence on the function of reaction networks on several biomembranes.
Spatial-temporal scale and volume fraction of the present model.
The authors are grateful to Y. Togashi, K. Takahashi, K. Aoki, M. Nishikawa and M. Kikuchi for the fruitful discussion and useful information.
Conceived and designed the model: MF AA HN. Performed the simulation: MF. Analyzed data: MF. Contributed theoretical analysis: MF AA. Wrote the paper: MF AA.
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