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. 1981 Jun;32(3):1216–1226. doi: 10.1128/iai.32.3.1216-1226.1981

Psoralen inactivation of influenza and herpes simplex viruses and of virus-infected cells.

D C Redfield, D D Richman, M N Oxman, L H Kronenberg
PMCID: PMC351582  PMID: 6265375

Abstract

Psoralen compounds covalently bind to nucleic acids when irradiated with long-wavelength ultraviolet light. This treatment can destroy the infectivity of deoxyribonucleic acid and ribonucleic acid viruses. Two psoralen compounds, 4'-hydroxymethyltrioxsalen and 4'-aminomethyltrioxsalen, were used with long-wavelength ultraviolet light to inactivate cell-free herpes simplex and influenza viruses and to render virus-infected cells noninfectious. This method of inactivation was compared with germicidal (short-wavelength) ultraviolet light irradiation. The antigenicity of the treated, virus-infected, antigen-bearing cells was examined by immunofluorescence and radioimmunoassay and by measuring the capacity of the herpes simplex virus-infected cells to stimulate virus-specific lymphocyte proliferation. The infectivity of the virus-infected cells could be totally eliminated without altering their viral antigenicity. The use of psoralen plus long-wavelength ultraviolet light is well suited to the preparation of noninfectious virus antigens and virus antigen-bearing cells for immunological assays.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. COULSON A. S., CHALMERS D. G. SEPARATION OF VIABLE LYMPHOCYTES FROM HUMAN BLOOD. Lancet. 1964 Feb 29;1(7331):468–469. doi: 10.1016/s0140-6736(64)90799-8. [DOI] [PubMed] [Google Scholar]
  2. Cleveland P. H., Richman D. D., Oxman M. N., Wickham M. G., Binder P. S., Worthen D. M. Immobilization of viral antigens on filter paper for a [125I]staphylococcal protein A immunoassay: a rapid and sensitive technique for detection of herpes simplex virus antigens and antiviral antibodies. J Immunol Methods. 1979;29(4):369–386. doi: 10.1016/0022-1759(79)90008-5. [DOI] [PubMed] [Google Scholar]
  3. Cole R. S. Light-induced cross-linking of DNA in the presence of a furocoumarin (psoralen). Studies with phage lambda, Escherichia coli, and mouse leukemia cells. Biochim Biophys Acta. 1970 Sep 17;217(1):30–39. doi: 10.1016/0005-2787(70)90119-x. [DOI] [PubMed] [Google Scholar]
  4. Hallick L. M., Yokota H. A., Bartholomew J. C., Hearst J. E. Photochemical addition of the cross-linking reagent 4,5', 8-trimethylpsoralen (trioxaslen) to intracellular and viral simian virus 40 DNA-histone complexes. J Virol. 1978 Jul;27(1):127–135. doi: 10.1128/jvi.27.1.127-135.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Hanson C. V., Riggs J. L., Lennette E. H. Photochemical inactivation of DNA and RNA viruses by psoralen derivatives. J Gen Virol. 1978 Aug;40(2):345–358. doi: 10.1099/0022-1317-40-2-345. [DOI] [PubMed] [Google Scholar]
  6. Hearst J. E., Thiry L. The photoinactivation of an RNA animal virus, vesicular stomatitis virus, with the aid of newly synthesized psoralen derivatives. Nucleic Acids Res. 1977;4(5):1339–1347. doi: 10.1093/nar/4.5.1339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Hochkeppel H. K., Gordon J. Evidence for cross-linking of polyribonucleotides with 4'-aminomethyl-4,5',8-trimethylpsoralen hydrochloride. Biochemistry. 1979 Jun 26;18(13):2905–2910. doi: 10.1021/bi00580a035. [DOI] [PubMed] [Google Scholar]
  8. Hodes H. L., Lavin G. I., Webster L. T. ANTIRABIC IMMUNIZATION WITH CULTURE VIRUS RENDERED AVIRULENT BY ULTRA-VIOLET LIGHT. Science. 1937 Nov 12;86(2237):447–448. doi: 10.1126/science.86.2237.447. [DOI] [PubMed] [Google Scholar]
  9. Howard-Flanders P., Lin P. F. Genetic recombination induced by DNA cross-links in repressed phage lambda. Genetics. 1973 Apr;73(Suppl):85–90. [PubMed] [Google Scholar]
  10. Hyde J. E., Hearst J. E. Binding of psoralen derivatives to DNA and chromatin: influence of the ionic environment on dark binding and photoreactivity. Biochemistry. 1978 Apr 4;17(7):1251–1257. doi: 10.1021/bi00600a019. [DOI] [PubMed] [Google Scholar]
  11. Isaacs S. T., Shen C. K., Hearst J. E., Rapoport H. Synthesis and characterization of new psoralen derivatives with superior photoreactivity with DNA and RNA. Biochemistry. 1977 Mar 22;16(6):1058–1064. doi: 10.1021/bi00625a005. [DOI] [PubMed] [Google Scholar]
  12. MUSAJO L., RODIGHIERO G., COLOMBO G., TORLONE V., DALLACQUA F. PHOTOSENSITIZING FUROCOUMARINS: INTERACTION WITH DNA AND PHOTO-INACTIVATION OF DNA CONTAINING VIRUSES. Experientia. 1965 Jan 15;21:22–24. doi: 10.1007/BF02136362. [DOI] [PubMed] [Google Scholar]
  13. Musajo L., Bordin F., Caporale G., Marciani S., Rigatti G. Photoreactions at 3655 Angstrom between pyrimidine bases and skin-photosensitizing furocoumarins. Photochem Photobiol. 1967 Oct;6(10):711–719. doi: 10.1111/j.1751-1097.1967.tb08736.x. [DOI] [PubMed] [Google Scholar]
  14. Nakashima K., Chanda P. K., Deutsch V., Banerjee A. K., Shatkin A. J. Inactivation of influenza and vesicular stomatitis virion RNA polymerase activities by photoreaction with 4'-substituted psoralens. J Virol. 1979 Dec;32(3):838–844. doi: 10.1128/jvi.32.3.838-844.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Nakashima K., Shatkin A. J. Photochemical cross-linking of reovirus genome RNA in situ and inactivation of viral transcriptase. J Biol Chem. 1978 Dec 25;253(24):8680–8682. [PubMed] [Google Scholar]
  16. Notkins A. L. Immune mechanisms by which the spread of viral infections is stopped. Cell Immunol. 1974 Mar 30;11(1-3):478–483. doi: 10.1016/0008-8749(74)90045-8. [DOI] [PubMed] [Google Scholar]
  17. Plaeger-Marshall S., Smith J. W. Inhibition of mitogen- and antigen-induced lymphocyte blastogenesis by herpes simplex virus. J Infect Dis. 1978 Oct;138(4):506–511. doi: 10.1093/infdis/138.4.506. [DOI] [PubMed] [Google Scholar]
  18. Rosenberg G. L., Farber P. A., Notkins A. L. In vitro stimulation of sensitized lymphocytes by herpes simplex virus and vaccinia virus. Proc Natl Acad Sci U S A. 1972 Mar;69(3):756–760. doi: 10.1073/pnas.69.3.756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. Russell A. S. Cell-mediated immunity to herpes simplex virus in man. Am J Clin Pathol. 1973 Dec;60(6):826–830. doi: 10.1093/ajcp/60.6.826. [DOI] [PubMed] [Google Scholar]
  20. Scott B. R., Pathak M. A., Mohn G. R. Molecular and genetic basis of furocoumarin reactions. Mutat Res. 1976;39(1):29–74. doi: 10.1016/0165-1110(76)90012-9. [DOI] [PubMed] [Google Scholar]
  21. Shen C. K., Hearst J. E. Psoralen-crosslinked secondary structure map of single-stranded virus DNA. Proc Natl Acad Sci U S A. 1976 Aug;73(8):2649–2653. doi: 10.1073/pnas.73.8.2649. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Shen C. K., Hsieh T. S., Wang J. C., Hearst J. E. Photochemical cross-linking of DNA-RNA helices by psoralen derivatives. J Mol Biol. 1977 Nov;116(4):661–679. doi: 10.1016/0022-2836(77)90265-0. [DOI] [PubMed] [Google Scholar]
  23. Sissons J. G., Oldstone M. B. Killing of virus-infected cells by cytotoxic lymphocytes. J Infect Dis. 1980 Jul;142(1):114–119. doi: 10.1093/infdis/142.1.114. [DOI] [PubMed] [Google Scholar]
  24. Song P. S., Tapley K. J., Jr Photochemistry and photobiology of psoralens. Photochem Photobiol. 1979 Jun;29(6):1177–1197. doi: 10.1111/j.1751-1097.1979.tb07838.x. [DOI] [PubMed] [Google Scholar]
  25. Zaia J. A., Oxman M. N. Antibody to varicella-zoster virus-induced membrane antigen: immunofluorescence assay using monodisperse glutaraldehyde-fixed target cells. J Infect Dis. 1977 Oct;136(4):519–530. doi: 10.1093/infdis/136.4.519. [DOI] [PubMed] [Google Scholar]

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