{"title":"A Stochastic Performance Analysis Framework for DNA-Based Authentication Protocols","authors":"Oriel Limor;Roy Shafir;Zohar Yakhini","doi":"10.1109/TMBMC.2026.3725619","DOIUrl":null,"url":null,"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 <inline-formula> <tex-math>$n$ </tex-math></inline-formula> 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 (<inline-formula> <tex-math>$\\mathcal {M}$ </tex-math></inline-formula>), the customer (<inline-formula> <tex-math>$\\mathcal {C}$ </tex-math></inline-formula>), and an adversary (<inline-formula> <tex-math>$\\mathcal {A}$ </tex-math></inline-formula>). After receiving the product, <inline-formula> <tex-math>$\\mathcal {C}\\ $ </tex-math></inline-formula> obtains verification challenges from <inline-formula> <tex-math>$\\mathcal {M}$ </tex-math></inline-formula>, applies them to the DNA embedded in the product, and sends the resulting pattern back to <inline-formula> <tex-math>$\\mathcal {M}\\ $ </tex-math></inline-formula> for verification. Meanwhile, <inline-formula> <tex-math>$\\mathcal {A}\\ $ </tex-math></inline-formula> attempts to counterfeit products by imitating the tagging signature based on observed results. We propose a performance indicator that quantifies <inline-formula> <tex-math>$\\mathcal {A}$ </tex-math></inline-formula>’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.","PeriodicalId":36530,"journal":{"name":"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications","volume":"12 ","pages":"937-946"},"PeriodicalIF":2.5000,"publicationDate":"2026-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ieeexplore.ieee.org/stamp/stamp.jsp?tp=&arnumber=11660756","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications","FirstCategoryId":"1085","ListUrlMain":"https://ieeexplore.ieee.org/document/11660756/","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/20 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
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.
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.