A Stochastic Performance Analysis Framework for DNA-Based Authentication Protocols

IF 2.5 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC
Oriel Limor;Roy Shafir;Zohar Yakhini
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引用次数: 0

Abstract

Synthetic DNA is gaining significant attention for its potential across various fields, both in biology and as an information medium. One particular emerging field of application is product tagging, driven by the need for enhanced security, precise traceability, and reliable authenticity verification. The field of DNA-based authentication protocols is still in its early stages. In this work we propose a framework for analyzing and comparing the performance of such protocols. We introduce precise definitions and present analytical results. We evaluate two representative protocols inspired by research published in recent literature. The first protocol employs the whole genome of a cell line with mutations at $n$ specific locations and the second uses Chemical Unclonable Functions (CUFs), inducing unique patterns based on primer pair challenges. We model the interaction between three entities: the manufacturer ( $\mathcal {M}$ ), the customer ( $\mathcal {C}$ ), and an adversary ( $\mathcal {A}$ ). After receiving the product, $\mathcal {C}\ $ obtains verification challenges from $\mathcal {M}$ , applies them to the DNA embedded in the product, and sends the resulting pattern back to $\mathcal {M}\ $ for verification. Meanwhile, $\mathcal {A}\ $ attempts to counterfeit products by imitating the tagging signature based on observed results. We propose a performance indicator that quantifies $\mathcal {A}$ ’s success probability as a function of the number of observed product instances and on the signature complexity. Finally, we discuss key challenges and propose optimization approaches to strengthen protocol resilience.
基于dna认证协议的随机性能分析框架
合成DNA因其在生物学和作为信息媒介等各个领域的潜力而受到广泛关注。一个特定的新兴应用领域是产品标签,这是由增强安全性、精确的可追溯性和可靠的真实性验证的需求驱动的。基于dna的认证协议领域仍处于早期阶段。在这项工作中,我们提出了一个框架来分析和比较这些协议的性能。我们引入了精确的定义并给出了分析结果。我们评估了两个代表性的协议,灵感来自于最近发表的研究文献。第一种方案使用在特定位置突变的细胞系的全基因组,第二种方案使用化学不可克隆功能(CUFs),基于引物对挑战诱导独特的模式。我们对三个实体之间的交互进行建模:制造商($\mathcal {M}$)、客户($\mathcal {C}$)和对手($\mathcal {A}$)。在收到产品后,$\mathcal {C}\ $从$\mathcal {M}$获得验证挑战,将其应用于嵌入在产品中的DNA,并将结果模式发送回$\mathcal {M}\ $进行验证。同时,$\mathcal {A}\ $根据观察到的结果,试图通过模仿标签签名来假冒产品。我们提出了一个性能指标,将$\mathcal {a}$的成功概率量化为观察到的产品实例数量和签名复杂性的函数。最后,我们讨论了关键挑战,并提出了增强协议弹性的优化方法。
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来源期刊
CiteScore
3.90
自引率
13.60%
发文量
23
期刊介绍: As a result of recent advances in MEMS/NEMS and systems biology, as well as the emergence of synthetic bacteria and lab/process-on-a-chip techniques, it is now possible to design chemical “circuits”, custom organisms, micro/nanoscale swarms of devices, and a host of other new systems. This success opens up a new frontier for interdisciplinary communications techniques using chemistry, biology, and other principles that have not been considered in the communications literature. The IEEE Transactions on Molecular, Biological, and Multi-Scale Communications (T-MBMSC) is devoted to the principles, design, and analysis of communication systems that use physics beyond classical electromagnetism. This includes molecular, quantum, and other physical, chemical and biological techniques; as well as new communication techniques at small scales or across multiple scales (e.g., nano to micro to macro; note that strictly nanoscale systems, 1-100 nm, are outside the scope of this journal). Original research articles on one or more of the following topics are within scope: mathematical modeling, information/communication and network theoretic analysis, standardization and industrial applications, and analytical or experimental studies on communication processes or networks in biology. Contributions on related topics may also be considered for publication. Contributions from researchers outside the IEEE’s typical audience are encouraged.
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