This study presents a rapid, ultrasound-assisted solid-liquid extraction protocol for recovering peptides from the tooth surface, while preserving the macroscopically visible integrity of the dental morphology. The methodology described herein enables the concurrent use of a single peptide extraction for multiple analytical objectives, encompassing: (i) biological sex determination via detection of sex-dimorphic amelogenin isoforms; (ii) dietary reconstruction based on the identification of food-derived protein residues; (iii) oral microbiome profiling to infer historical health status and disease burden; and (iv) an assessment of age-at-death (AAD) estimation through quantification of asparagine and glutamine deamidation kinetics. Peptide extraction is achieved through an ultrasound-assisted solid–liquid interface, facilitating the release of biomolecules embedded within the dental tissues' matrix without producing macroscopically detectable damage to the sample. The resulting peptide fraction undergoes purification using hydrophilic-lipophilic balanced (HLB) cartridges and is subsequently analysed via high-resolution mass spectrometry. The protocol offers notable advantages, including speed, reproducibility, high throughput, and alignment with the principles of analytical minimalism. Collectively, this strategy represents a substantial advancement in non-invasive dental peptidomics, providing a robust and minimally destructive analytical framework for forensic and bioarchaeological investigations.
Andre, C.A.P., Fonseca, R., Figueiredo, A.Q., Lodeiro, C., Benazzi, S., Belcastro, M.G., et al. (2026). Fast ultrasonic-based extraction of peptides from teeth for forensics and archaeological purposes. MICROCHEMICAL JOURNAL, 221, 1-8 [10.1016/j.microc.2026.116915].
Fast ultrasonic-based extraction of peptides from teeth for forensics and archaeological purposes
Benazzi S.;Belcastro M. G.;
2026
Abstract
This study presents a rapid, ultrasound-assisted solid-liquid extraction protocol for recovering peptides from the tooth surface, while preserving the macroscopically visible integrity of the dental morphology. The methodology described herein enables the concurrent use of a single peptide extraction for multiple analytical objectives, encompassing: (i) biological sex determination via detection of sex-dimorphic amelogenin isoforms; (ii) dietary reconstruction based on the identification of food-derived protein residues; (iii) oral microbiome profiling to infer historical health status and disease burden; and (iv) an assessment of age-at-death (AAD) estimation through quantification of asparagine and glutamine deamidation kinetics. Peptide extraction is achieved through an ultrasound-assisted solid–liquid interface, facilitating the release of biomolecules embedded within the dental tissues' matrix without producing macroscopically detectable damage to the sample. The resulting peptide fraction undergoes purification using hydrophilic-lipophilic balanced (HLB) cartridges and is subsequently analysed via high-resolution mass spectrometry. The protocol offers notable advantages, including speed, reproducibility, high throughput, and alignment with the principles of analytical minimalism. Collectively, this strategy represents a substantial advancement in non-invasive dental peptidomics, providing a robust and minimally destructive analytical framework for forensic and bioarchaeological investigations.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.


