Recent advances in the synthesis and structure determination of site specifically psoralen-modified DNA oligonucleotides

Srinivas S. Sastry; H. Peter Spielmann; Tammy J. Dwyer; David E. Wemmer; John E. Hearst

doi:10.1016/1011-1344(92)85083-7

Recent advances in the synthesis and structure determination of site specifically psoralen-modified DNA oligonucleotides

Srinivas S. Sastry
, H. Peter Spielmann
, Tammy J. Dwyer
, David E. Wemmer
, John E. Hearst

Producción científica: Article › revisión exhaustiva

12 Citas (Scopus)

Resumen

We have developed novel methods for the preparation of multimicromole quantities of extremely pure, uniquely photoadducted psoralen-DNA cross-links, furan-side monoadducts and pyrone-side monoadducts. Psoralen cross-linked and furan-side monoadducted DNA were produced by employing high intensity argon ion and krypton ion lasers as light sources. Pyrone-side monoadducts were prepared by base-catalyzed photoreversal of psoralen cross-links. The various psoralen-adducted DNA oligomers were efficiently purified by high performance liquid chromatography. These methods have permitted us to synthesize 4 μmol each of a self-complementary 8-mer d(GCGTACGC) 4′-(hydroxymethyl)-4,5′,8-trimethylpsoralen (HMT) furan-side monoadduct and HMT cross-link. Preliminary nuclear magnetic resonance (NMR) data on the HMT cross-linked 8-mer d(GCGTACGC) have been obtained which confirmed the presence of the diadducted psoralen at the unique 5′TpA3′ site. NMR data obtained from the 8-mer furan-side monoadduct revealed that the psoralen molecule is intercalated into the DNA double helix. Preliminary crystals of 8-mer cross-linked DNA molecule have been grown. Conditions for the growth of X-ray diffraction-quality crystals and the further analysis of these crystals are now in progress.

Idioma original	English
Páginas (desde-hasta)	65-79
Número de páginas	15
Publicación	Journal of Photochemistry and Photobiology, B: Biology
Volumen	14
N.º	1-2
DOI	https://doi.org/10.1016/1011-1344(92)85083-7
Estado	Published - jun 30 1992

Nota bibliográfica

Funding Information:
We are thankful to Dr. David Cook for advice and suggestionsd uring the course of the experimentsa nd the laser training course and Mr. David Koh for oligonucleotide synthesis. We thank Professor R. Mathies and Dr. J. Ames for their help with the use of the krypton laser. The various suggestions and help of the members of the Hearst Laboratory are also appreciated. This work was supported by the Director, Office of Energy Research, Office of General Life Sciences,M olecular Biology Division (J.E.H.) and Office of Energy Research, Office of Health and Environmental Research (D.E.W.) of the US Department of Energy under Contract DE-ACO3-76SF00098 and National Institute of Health Grant GM 41911t o J.E.H. S.S.S. was supported by Grant NIEHS 07075-11 from United States Public Health Service. Instrumentation was provided by US Department of Energy Grant DE FGOS-86ER75281 and National Science Foundation Grants DMB86-09035 and BBS87-20134.

Financiación

We are thankful to Dr. David Cook for advice and suggestionsd uring the course of the experimentsa nd the laser training course and Mr. David Koh for oligonucleotide synthesis. We thank Professor R. Mathies and Dr. J. Ames for their help with the use of the krypton laser. The various suggestions and help of the members of the Hearst Laboratory are also appreciated. This work was supported by the Director, Office of Energy Research, Office of General Life Sciences,M olecular Biology Division (J.E.H.) and Office of Energy Research, Office of Health and Environmental Research (D.E.W.) of the US Department of Energy under Contract DE-ACO3-76SF00098 and National Institute of Health Grant GM 41911t o J.E.H. S.S.S. was supported by Grant NIEHS 07075-11 from United States Public Health Service. Instrumentation was provided by US Department of Energy Grant DE FGOS-86ER75281 and National Science Foundation Grants DMB86-09035 and BBS87-20134.

Financiadores	Número del financiador
National Institutes of Health/National Institute of Environmental Health Sciences	GM 41911t, NIEHS 07075-11
Office of Energy Research
Office of General Life Sciences
Office of Health and Environmental Research
US Department of Energy	DE-ACO3-76SF00098
National Science Foundation Arctic Social Science Program	DMB86-09035, BBS87-20134
National Science Foundation Arctic Social Science Program
National Institute of General Medical Sciences	R01GM041911
National Institute of General Medical Sciences
U.S. Public Health Service	DE FGOS-86ER75281
U.S. Public Health Service

ASJC Scopus subject areas

Radiation
Radiological and Ultrasound Technology
Biophysics
Radiology Nuclear Medicine and imaging

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10.1016/1011-1344(92)85083-7

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title = "Recent advances in the synthesis and structure determination of site specifically psoralen-modified DNA oligonucleotides",

abstract = "We have developed novel methods for the preparation of multimicromole quantities of extremely pure, uniquely photoadducted psoralen-DNA cross-links, furan-side monoadducts and pyrone-side monoadducts. Psoralen cross-linked and furan-side monoadducted DNA were produced by employing high intensity argon ion and krypton ion lasers as light sources. Pyrone-side monoadducts were prepared by base-catalyzed photoreversal of psoralen cross-links. The various psoralen-adducted DNA oligomers were efficiently purified by high performance liquid chromatography. These methods have permitted us to synthesize 4 μmol each of a self-complementary 8-mer d(GCGTACGC) 4′-(hydroxymethyl)-4,5′,8-trimethylpsoralen (HMT) furan-side monoadduct and HMT cross-link. Preliminary nuclear magnetic resonance (NMR) data on the HMT cross-linked 8-mer d(GCGTACGC) have been obtained which confirmed the presence of the diadducted psoralen at the unique 5′TpA3′ site. NMR data obtained from the 8-mer furan-side monoadduct revealed that the psoralen molecule is intercalated into the DNA double helix. Preliminary crystals of 8-mer cross-linked DNA molecule have been grown. Conditions for the growth of X-ray diffraction-quality crystals and the further analysis of these crystals are now in progress.",

keywords = "DNA photoadducts, Lasers, high performance liquid chromatography, nuclear magnetic resonance., photochemistry, psoralen",

author = "Sastry, \{Srinivas S.\} and Spielmann, \{H. Peter\} and Dwyer, \{Tammy J.\} and Wemmer, \{David E.\} and Hearst, \{John E.\}",

note = "Funding Information: We are thankful to Dr. David Cook for advice and suggestionsd uring the course of the experimentsa nd the laser training course and Mr. David Koh for oligonucleotide synthesis. We thank Professor R. Mathies and Dr. J. Ames for their help with the use of the krypton laser. The various suggestions and help of the members of the Hearst Laboratory are also appreciated. This work was supported by the Director, Office of Energy Research, Office of General Life Sciences,M olecular Biology Division (J.E.H.) and Office of Energy Research, Office of Health and Environmental Research (D.E.W.) of the US Department of Energy under Contract DE-ACO3-76SF00098 and National Institute of Health Grant GM 41911t o J.E.H. S.S.S. was supported by Grant NIEHS 07075-11 from United States Public Health Service. Instrumentation was provided by US Department of Energy Grant DE FGOS-86ER75281 and National Science Foundation Grants DMB86-09035 and BBS87-20134.",

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doi = "10.1016/1011-1344(92)85083-7",

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AU - Sastry, Srinivas S.

AU - Spielmann, H. Peter

AU - Dwyer, Tammy J.

AU - Wemmer, David E.

AU - Hearst, John E.

N1 - Funding Information: We are thankful to Dr. David Cook for advice and suggestionsd uring the course of the experimentsa nd the laser training course and Mr. David Koh for oligonucleotide synthesis. We thank Professor R. Mathies and Dr. J. Ames for their help with the use of the krypton laser. The various suggestions and help of the members of the Hearst Laboratory are also appreciated. This work was supported by the Director, Office of Energy Research, Office of General Life Sciences,M olecular Biology Division (J.E.H.) and Office of Energy Research, Office of Health and Environmental Research (D.E.W.) of the US Department of Energy under Contract DE-ACO3-76SF00098 and National Institute of Health Grant GM 41911t o J.E.H. S.S.S. was supported by Grant NIEHS 07075-11 from United States Public Health Service. Instrumentation was provided by US Department of Energy Grant DE FGOS-86ER75281 and National Science Foundation Grants DMB86-09035 and BBS87-20134.

PY - 1992/6/30

Y1 - 1992/6/30

N2 - We have developed novel methods for the preparation of multimicromole quantities of extremely pure, uniquely photoadducted psoralen-DNA cross-links, furan-side monoadducts and pyrone-side monoadducts. Psoralen cross-linked and furan-side monoadducted DNA were produced by employing high intensity argon ion and krypton ion lasers as light sources. Pyrone-side monoadducts were prepared by base-catalyzed photoreversal of psoralen cross-links. The various psoralen-adducted DNA oligomers were efficiently purified by high performance liquid chromatography. These methods have permitted us to synthesize 4 μmol each of a self-complementary 8-mer d(GCGTACGC) 4′-(hydroxymethyl)-4,5′,8-trimethylpsoralen (HMT) furan-side monoadduct and HMT cross-link. Preliminary nuclear magnetic resonance (NMR) data on the HMT cross-linked 8-mer d(GCGTACGC) have been obtained which confirmed the presence of the diadducted psoralen at the unique 5′TpA3′ site. NMR data obtained from the 8-mer furan-side monoadduct revealed that the psoralen molecule is intercalated into the DNA double helix. Preliminary crystals of 8-mer cross-linked DNA molecule have been grown. Conditions for the growth of X-ray diffraction-quality crystals and the further analysis of these crystals are now in progress.

AB - We have developed novel methods for the preparation of multimicromole quantities of extremely pure, uniquely photoadducted psoralen-DNA cross-links, furan-side monoadducts and pyrone-side monoadducts. Psoralen cross-linked and furan-side monoadducted DNA were produced by employing high intensity argon ion and krypton ion lasers as light sources. Pyrone-side monoadducts were prepared by base-catalyzed photoreversal of psoralen cross-links. The various psoralen-adducted DNA oligomers were efficiently purified by high performance liquid chromatography. These methods have permitted us to synthesize 4 μmol each of a self-complementary 8-mer d(GCGTACGC) 4′-(hydroxymethyl)-4,5′,8-trimethylpsoralen (HMT) furan-side monoadduct and HMT cross-link. Preliminary nuclear magnetic resonance (NMR) data on the HMT cross-linked 8-mer d(GCGTACGC) have been obtained which confirmed the presence of the diadducted psoralen at the unique 5′TpA3′ site. NMR data obtained from the 8-mer furan-side monoadduct revealed that the psoralen molecule is intercalated into the DNA double helix. Preliminary crystals of 8-mer cross-linked DNA molecule have been grown. Conditions for the growth of X-ray diffraction-quality crystals and the further analysis of these crystals are now in progress.

KW - DNA photoadducts

KW - Lasers

KW - high performance liquid chromatography

KW - nuclear magnetic resonance.

KW - photochemistry

KW - psoralen

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Recent advances in the synthesis and structure determination of site specifically psoralen-modified DNA oligonucleotides

Resumen

Nota bibliográfica

Financiación

ASJC Scopus subject areas

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