High‐throughput seminal fluid identification by automated immunoaffinity mass spectrometry
Abstract
The identification of semen during a criminal investigation may be a critical component in the prosecution of a sexual assault. Commonly employed enzymatic and affinity‐based methods for detection lack specificity, are time‐consuming, and only provide a presumptive indication that semen is present where microscopic visualization is unable to meet the throughput demands. Contrary to traditional approaches, protein mass spectrometry provides true confirmatory results, but multiday sample preparation and nanoflow sample separation requirements have limited the practical applicability of these approaches. Aiming at streamlining sexual assault screening by mass spectrometry, the work here coupled a 60‐minute rapid tryptic digestion, semenogelin‐II peptide affinity purification on an Agilent AssayMap Bravo automation platform, and a 3‐minute targeted LC‐MS/MS method on an Agilent 6495 triple quadrupole mass spectrometer operating in multiple reaction monitoring mode for detecting semenogelin‐II peptides in sexual assault samples. The developed assay was assessed using casework‐type samples and was successful in detecting trace levels (0.0001 μl) of semen recovered from both cotton and vaginal swabs, as well as semen recovered from vaginal swabs during menses or adulterated with personal lubricants. This work represents a promising technique for high‐throughput seminal fluid identification in sexual assault‐type samples by mass spectrometry.
Document Details
- Document Type
- Pub Defense Publication
- Publication Date
- Jan 13, 2022
- Source ID
- 10.1111/1556-4029.14975
Entities
People
- Catherine O. Brown
- Heather E. Mckiernan
- Kevin M. Legg
- Mechthild Prinz
- Phillip B. Danielson
- Rachel Davidovics
- Yih Ling Saw
Organizations
- Arcadia University
- John Jay College of Criminal Justice
- Thomas Jefferson University
- United States Army
- University of Denver