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Solvation and hydration are key factors for determining the stability and folding of proteins, as well as the formation of amyloid fibrils and related polypeptide aggregates. Using attenuated total reflectance Fourier-transform infrared and solid-state NMR spectroscopy, we find that the Aβ peptide experiences a remarkable conformational switch from β to α secondary structure upon solvent removal by lyophilization of oligomers. This transition is, contrary to Aβ fibrils, independent of concentration of organic co-solvents or co-solutes and is reversible upon re-addition of the solvent. Our data illuminate a previously unnoted secondary structural plasticity of the Aβ peptide in amyloid oligomers that could bear relevance for Aβ's interactions with cellular structures of low polarity.

Heteronuclear dipolar decoupling in MAS solid state NMR studies of biological systems has been investigated at moderate spinning speeds. It is shown that the efficacy of C N n ν symmetry-based decoupling schemes with tanh/tan adiabatic pulses can be significantly improved by optimising the amplitude and frequency modulation characteristics of the inversion pulses employed. The decoupling performance of the symmetry-based schemes is compared with that of the commonly used TPPM technique.

It is shown that it is possible to carry out with only a moderate RF field strength of ⩽40 kHz, even at high magic angle spinning frequencies, broadband homonuclear double-quantum filtered 13 C chemical shift correlation and double-quantum solid state NMR studies of biological systems via the zero-quantum dipolar recoupling sequence RFDR.

The performance of symmetry-based adiabatic RF pulse schemes for 1 H decoupling at moderate magic angle spinning (MAS) frequencies has been evaluated via numerical simulations and experimentally compared with other decoupling techniques. Our studies reveal that in MAS solid state NMR studies of polycrystalline specimens, in contrast to symmetry-based RF pulse schemes involving rectangular RF pulses, adiabatic decoupling sequences can be effectively implemented to make use of all the available decoupling RF field strength and to eliminate the deleterious effects of H 1 inhomogeneity and resonance offset. Symmetry-based adiabatic decoupling sequences lead to improved decoupling performance compared to a continuous train of adiabatic inversion pulses that are phase cycled as in solution state NMR studies.

In a dipolar-coupled spin-1/2 network of the type 15 N1– 13 C– 15 N2, an assessment of the sensitivity of the N → C and C → N TEDOR sideband intensities to the Euler angles defining the orientation of the two heteronuclear dipolar vectors in the 13 C and 15 N chemical shift (CS) tensor principal axes system has been carried out via numerical calculations. The results clearly indicate the potential of TEDOR MAS NMR spectroscopy for the characterization of the CS tensor orientation in the molecular frame. The efficacy of the method has been experimentally illustrated by TEDOR studies on a polycrystalline sample of [1,3— 15 N 2 , 2— 13 C]uracil, which is one of the four bases in RNA.

The response of a spin (1/2) ensemble, at thermal equilibrium and experiencing chemical shift anisotropy (CSA), to the application of adiabatic inversion pulses has been studied under magic-angle spinning (MAS). Numerical simulations and experimental studies on such systems, carried out under slow spinning conditions, show that the response to adiabatic inversion pulses has much more favorable characteristics than the response to conventional rectangular pulses. We have also explored the possibilities of employing adiabatic 180 degrees pulses as dephasing pulses in rotational-echo double-resonance (REDOR) experiments. Our results show that it is indeed possible to employ such adiabatic inversion pulses conveniently in REDOR experiments to eliminate resonance offset and H(1) inhomogeneity effects which may arise from the usage of conventional rectangular 180 degrees pulses. Copyright 2000 Academic Press.

As part of our studies on the characterization of 15N chemical shift anisotropy (CSA) via magic angle spinning (MAS) NMR spectroscopy, we have investigated via numerical simulations the sensitivity of two different REDOR experimental protocols to the angles defining the orientation of the 15N-13C' bond vector in the principal axis system of the 15N CSA tensor of the amide nitrogen in a peptide bond. Additionally, employing polycrystalline samples of 15N and 13C', 15N-labeled acetanilide, we have obtained, in a first study of this type, the orientation of the 15N CSA tensor in the molecular frame by orienting the tensor with respect to the 15N-3C' and 15N-1H dipolar vectors via 15N-13C' REDOR and 15N-1H dipolar-shift MAS experiments, respectively.