Source abstract
Abstract
Abstract A Physical Unclonable Function (PUF) is a security primitive that exploits inherent variations in manufacturing protocols to generate unique, random‐like identifiers. These identifiers are used for authentication and encryption purposes in hardware security applications in the semiconductor industry. Inspired by the success of silicon PUFs, herein it is leverage Terminal deoxynucleotidyl Transferase (TdT), a template‐independent polymerase belonging to the X‐family of DNA polymerases, to augment the intrinsic entropy generated during DNA lesion repair and rapidly produce genetic PUFs that satisfy the following properties: robustness (i.e., they repeatedly produce the same output), uniqueness (i.e., they do not coincide with any other identically produced PUF), and unclonability (i.e., they are virtually impossible to replicate). Furthermore, a post‐sequencing feature selection methodology based on logistic regression to facilitate PUF classification is developed. This experimental and computational pipeline drastically reduces production time and cost compared to conventional genetic barcoding without compromising the stringent PUF criteria of uniqueness and unclonability. This results provide novel insights into the function of TdT and represent a major step toward utilization of PUFs as a biosecurity primitive for cell line authentication and provenance attestation.
Source: crossref · Quality: baseline
Research context
OpenAlex topics: CRISPR and Genetic Engineering · Law, AI, and Intellectual Property · Physical Unclonable Functions (PUFs) and Hardware Security
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Bioengineering Department The University of Texas at Dallas Richardson Texas 75080 USA
Center for Systems Biology The University of Texas at Dallas Richardson Texas 75080 USA
Department of Electrical and Computer Engineering University of Texas at Dallas Richardson Texas 75080 USA
Department of Pediatrics The University of Texas Health Science Center at San Antonio San Antonio Texas 78229 USA
Department of Cell Systems & Anatomy The University of Texas Health Science Center at San Antonio San Antonio Texas 78229 USA
Greehey Children's Cancer Research Institute The University of Texas Health Science Center at San Antonio San Antonio Texas 78229 USA
Department of Biological Sciences The University of Texas at Dallas Richardson Texas 75080 USA
Funding
National Science Foundation
References (39)
Show source-provided references
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