Nucleotide-type chemical shift assignment of the encapsulated 40 kbp dsDNA in intact bacteriophage T7 by MAS solid-state NMR
被引:16
作者:
Abramov, Gili
论文数: 0引用数: 0
h-index: 0
机构:
Tel Aviv Univ, Sch Chem, Raymond & Beverly Sackler Fac Exact Sci, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Sch Chem, Raymond & Beverly Sackler Fac Exact Sci, IL-69978 Tel Aviv, Israel
Abramov, Gili
[1
]
Goldbourt, Amir
论文数: 0引用数: 0
h-index: 0
机构:
Tel Aviv Univ, Sch Chem, Raymond & Beverly Sackler Fac Exact Sci, IL-69978 Tel Aviv, IsraelTel Aviv Univ, Sch Chem, Raymond & Beverly Sackler Fac Exact Sci, IL-69978 Tel Aviv, Israel
Goldbourt, Amir
[1
]
机构:
[1] Tel Aviv Univ, Sch Chem, Raymond & Beverly Sackler Fac Exact Sci, IL-69978 Tel Aviv, Israel
The icosahedral bacteriophage T7 is a 50 MDa double-stranded DNA (dsDNA) virus that infects Escherichia coli. Although there is substantial information on the physical and morphological properties of T7, structural information, based mostly on Raman spectroscopy and cryo-electron microscopy, is limited. Here, we apply the magic-angle spinning (MAS) solid-state NMR (SSNMR) technique to study a uniformly C-13 and N-15 labeled wild-type T7 phage. We describe the details of the large-scale preparation and purification of an isotopically enriched phage sample under fully hydrated conditions, and show a complete C-13 and a near-complete N-15 nucleotide-type specific assignment of the sugar and base moieties in the 40 kbp dsDNA of T7 using two-dimensional C-13-C-13 and N-15-C-13 correlation experiments. The chemical shifts are interpreted as reporters of a B-form conformation of the encapsulated dsDNA. While MAS SSNMR was found to be extremely useful in determining the structures of proteins in native-like environments, its application to nucleic acids has lagged behind, leaving a missing C-13 and N-15 chemical shift database. This work therefore expands the C-13 and N-15 database of real B-form DNA systems, and opens routes to characterize more complex nucleic acid systems by SSNMR.
机构:
Univ Washington, Dept Biochem, Seattle, WA 98195 USA
Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USANIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
Vernon, Robert
Baker, David
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Dept Biochem, Seattle, WA 98195 USA
Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USANIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
机构:
Univ Washington, Dept Biochem, Seattle, WA 98195 USA
Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USANIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA
Vernon, Robert
Baker, David
论文数: 0引用数: 0
h-index: 0
机构:
Univ Washington, Dept Biochem, Seattle, WA 98195 USA
Univ Washington, Howard Hughes Med Inst, Seattle, WA 98195 USANIDDK, Chem Phys Lab, NIH, Bethesda, MD 20892 USA