Durmaz Merve Gorkem, Tulluk Neval, Aksoy Recep Deniz, Yilmaz Huseyin Birkan, Yang Bill, Wipat Anil, Pusane Ali Emre, Mısırlı Göksel, Tugcu Tuna
Department of Computer Engineering, NETLAB, Bogazici University, Bebek, Istanbul 34342, Turkiye.
School of Computing, Newcastle University, Newcastle upon Tyne NE4 5TG, United Kingdom.
Synth Biol (Oxf). 2024 Nov 7;9(1):ysae015. doi: 10.1093/synbio/ysae015. eCollection 2024.
Developments in bioengineering and nanotechnology have ignited the research on biological and molecular communication systems. Despite potential benefits, engineering communication systems to carry data signals using biological messenger molecules and engineered cells is challenging. Diffusing molecules may fall behind their schedule to arrive at the receiver, interfering with symbols of subsequent time slots and distorting the signal. Existing theoretical molecular communication models often focus solely on the characteristics of a communication channel and fail to provide an end-to-end system response since they assume a simple thresholding process for a receiver cell and overlook how the receiver can detect the incoming distorted molecular signal. In this paper, we present a model-based and computational framework called BioRxToolbox for designing diffusion-based and end-to-end molecular communication systems coupled with synthetic genetic circuits. We describe a novel framework to encode information as a sequence of bits, each transmitted from the sender as a burst of molecules, control cellular behavior at the receiver, and minimize cellular signal interference by employing equalization techniques from communication theory. This approach allows the encoding and decoding of data bits efficiently using two different types of molecules that act as the data carrier and the antagonist to cancel out the heavy tail of the former. Here, BioRxToolbox is demonstrated using a biological design and computational simulations for various communication scenarios. This toolbox facilitates automating the choice of communication parameters and identifying the best communication scenarios that can produce efficient cellular signals.
生物工程和纳米技术的发展引发了对生物和分子通信系统的研究。尽管有潜在的好处,但利用生物信使分子和工程细胞设计用于传输数据信号的通信系统具有挑战性。扩散的分子可能会延误到达接收器的时间,干扰后续时隙的符号并使信号失真。现有的理论分子通信模型通常只关注通信信道的特性,无法提供端到端的系统响应,因为它们假设接收器细胞采用简单的阈值处理过程,而忽略了接收器如何检测接收到的失真分子信号。在本文中,我们提出了一个基于模型的计算框架BioRxToolbox,用于设计与合成遗传电路相结合的基于扩散的端到端分子通信系统。我们描述了一种新颖的框架,将信息编码为比特序列,每个比特从发送方作为分子脉冲发送,控制接收器处的细胞行为,并通过采用通信理论中的均衡技术将细胞信号干扰降至最低。这种方法允许使用两种不同类型的分子有效地对数据比特进行编码和解码,这两种分子分别充当数据载体和拮抗剂,以抵消前者的重尾现象。在此,通过针对各种通信场景的生物设计和计算模拟展示了BioRxToolbox。该工具箱有助于自动选择通信参数,并识别能够产生高效细胞信号的最佳通信场景。