Monitoring human leukocyte antigen class I molecules by micro-raman spectroscopy at single-cell level

Gobind Das*, Rosanna La Rocca, Tadepally Lakshmikanth, Francesco Gentile, Rossana Tallerico, Lia P. Zambetti, J. Devitt, Patrizio Candeloro, Francesco De Angelis, Ennio Carbone, Enzo Di Fabrizio

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

19 Scopus citations

Abstract

Human leukocyte antigen (HLA) class I molecules are formed by three immunoglobulin-like domains (α1, α2, and α3) once folded by peptide and β 2-microglobulin show the presence of two α-helix streams and one β-sheet limiting the pocket for the antigenic peptide. The loss of HLA class I expression in tumors and virus-infected cells, on one hand, prevents T cell recognition, while on the other hand, it leads to natural killer (NK) cell mediated cytotoxicity. We propose the possibility of using Raman spectroscopy to measure the relative expression of HLA class I molecules at the single-cell level. Raman spectra are recorded for three cell lines (K562, T2, and T3) and monomers (HLA class I folded, unfolded and peptide+β 2-microlobulin refolded) using 830 nm laser line. Our data are consistent with the hypothesis that in the Raman spectra, ranging from 1600 to 1800 cm -1, the intensity variation of cells associated with HLA class I molecules could be measured.

Original languageEnglish (US)
Article number027007
JournalJournal of biomedical optics
Volume15
Issue number2
DOIs
StatePublished - 2010
Externally publishedYes

Keywords

  • Biomedical optics
  • Cells
  • Laser spectroscopy
  • Raman spectroscopy
  • Statistical optics
  • Vibration analysis

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Atomic and Molecular Physics, and Optics
  • Biomedical Engineering
  • Biomaterials

Fingerprint

Dive into the research topics of 'Monitoring human leukocyte antigen class I molecules by micro-raman spectroscopy at single-cell level'. Together they form a unique fingerprint.

Cite this