Solid-state NMR spectra contain a wealth of information regarding orientation of specific nuclei. The chemical shift anisotropy (CSA) can be represented as a second rank tensor with orientation dependence in its frequency distribution. The interpretation of the CSA frequency requires that the orientation of the elements of the tensor be mapped into the molecular frame of reference. The deoxyguanosine base was synthetically labeled with 15N in position N1. The tensor analysis was made by measuring the two-dimensional solid-state NMR PISEMA spectrum of the powder material. The one-dimensional 15N spectrum yields the principal elements of the CSA tensor and the two-dimensional spectrum can be simulated to determine the orientation of the 15N-1H dipolar coupling tensor relative to the CSA tensor. The orientation of the dipolar tensor is along the vector connecting the two nuclei, hence an anchor to the molecular frame of reference. The principal values of the 15N CSA tensor for the guanosine base are ?11= 54 ppm; ?22=108 ppm; and ?33=201 ppm relative to external ammonium sulfate. The simulated two-dimensional spectrum indicates that the ?33 element is colinear with the N-H bond. The principle elements ?11 and ?22 lie in the plane of the purine ring. This relation can now be used to elicit structural information from 15N chemical shift frequencies of oriented DNA.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR009793-05
Application #
6283004
Study Section
Project Start
1998-04-28
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
5
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Pennsylvania
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Valentine, Kathleen G; Mesleh, Michael F; Opella, Stanley J et al. (2003) Structure, topology, and dynamics of myristoylated recoverin bound to phospholipid bilayers. Biochemistry 42:6333-40
Montal, M; Opella, S J (2002) The structure of the M2 channel-lining segment from the nicotinic acetylcholine receptor. Biochim Biophys Acta 1565:287-93
Opella, Stanley J; DeSilva, Tara M; Veglia, Gianluigi (2002) Structural biology of metal-binding sequences. Curr Opin Chem Biol 6:217-23
Jiang, F; Gorin, A; Hu, W et al. (1999) Anchoring an extended HTLV-1 Rex peptide within an RNA major groove containing junctional base triples. Structure 7:1461-72
Marassi, F M; Ma, C; Gratkowski, H et al. (1999) Correlation of the structural and functional domains in the membrane protein Vpu from HIV-1. Proc Natl Acad Sci U S A 96:14336-41