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V Weis

Publications and source records attributed to V Weis.

5 recordsLinked to original sources

Electron-nuclear cross polarization.

We describe the coherent polarization transfer from an unpaired electron to neighboring nuclei via electron-nuclear cross polarization (eNCP) in a doubly, tilted rotating frame. Although the experiment superficially resembles the well-known Hartmann-Hahn cross polarization (CP) process introduced by Pines et al., that is widely used in solid-state nuclear magnetic resonance (SSNMR), it differs in significant respects. In particular, eNCP requires an alternative treatment due to the very different sizes of the specific terms in the spin Hamiltonian. We derive analytical expressions for the matching condition for optimal polarization transfer and verify their correctness with experimental results obtained with electron detected CP experiments performed on powder samples of BDPA radical dispersed in a protonated polystyrene matrix and with numerical simulations. We use fully protonated BDPA as an example of polarization transfer to strongly coupled nuclei. In contrast, perdeuterated BDPA serves as an example of the transfer of polarization from electrons to weakly coupled nuclei. In addition, we performed CP on a paramagnetic crystal to determine the influence of resolved hyperfine structure on the CP process. It is shown that almost no structure is observed in the corresponding electron-(1)H CP matching curve. It appears that only a restricted number of hyperfine coupled (1)H's contribute to the observed signal intensities in the CP experiment.

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Pulsed electron-nuclear double resonance (ENDOR) at 140 GHz.

We describe a spectrometer for pulsed ENDOR at 140 GHz, which is based on microwave IMPATT diode amplifiers and a probe consisting of a TE011 cavity with a high-quality resonance circuit for variable radiofrequency irradiation. For pulsed EPR we obtain an absolute sensitivity of 3x10(9) spins/Gauss at 20 K. The performance of the spectrometer is demonstrated with pulsed ENDOR spectra of a standard bis-diphenylene-phenyl-allyl (BDPA) doped into polystyrene and of the tyrosyl radical from E. coli ribonucleotide reductase (RNR). The EPR spectrum of the RNR tyrosyl radical displays substantial g-anisotropy at 5 T and is used to demonstrate orientation-selective Davies-ENDOR.

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High-field DNP and ENDOR with a novel multiple-frequency resonance structure.

We describe a new triply tuned (e(-), (1)H, and (13)C) resonance structure operating at an electron Larmor frequency of 139.5 GHz for dynamic nuclear polarization (DNP) and electron nuclear double-resonance (ENDOR) experiments. In contrast to conventional double-resonance structures, the body of the microwave cavity simultaneously acts as a NMR coil, allowing for increased efficiency of radiofrequency irradiation while maintaining a high quality factor for microwave irradiation. The resonator design is ideal for low-gamma-nuclei ENDOR, where sensitivity is limited by the fact that electron spin relaxation times are on the order of the RF pulse lengths. The performance is demonstrated with (2)H ENDOR on a standard perdeuterated bis-diphenylene-phenyl-allyl stable radical. In DNP experiments, we show that the use of this resonator, combined with a low microwave power setup (17 mW), leads to significantly higher (1)H signal enhancement (epsilon approximately 400 +/- 50) than previously achieved at 5-T fields. The results emphasize the importance of optimizing the microwave B(1) field by improving either the quality factor of the microwave resonator or the microwave power level.

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Optically detected electron spin echo envelope modulation on a photoexcited triplet state in zero magnetic field-A comparison between the zero-field and high-field limits

Electron spin echo envelope modulation (ESEEM) has been studied at zero and low magnetic fields (B </= 100 G) by means of optically detected magnetic resonance. Qualitative differences of the ESEEM effect for an electronic triplet state (S = 1) under low-field and high-field conditions are observed and discussed. They are related to the different properties of the total spin angular momentum operator S and the hyperfine interaction at zero and high magnetic field. The novel method was applied to the photoexcited triplet state of acridine-d9 in a fluorene-h10 matrix. An analysis of the observed nitrogen quadrupole splitting is done by a quantitative description of the ESEEM effect in zero field. Copyright 1998 Academic Press.

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Differential protein profiles reflect the different lifestyles of symbiotic and aposymbiotic Anthopleura elegantissima, a sea anemone from temperate waters

Mutualistic associations are prevalent in virtually all environments yet relatively little is known about their complex biochemical and molecular integration and regulation. The endosymbiosis between cnidarians such as the sea anemone Anthopleura elegantissima and the photosynthetic dinoflagellate Symbiodinium californium, in which the algal symbionts are housed in vacuoles within animal endodermal cells, is an ideal model for the study of highly integrated associations at the biochemical and molecular levels. This study describes differential protein synthesis between symbiotic A. elegantissima, collected from environments with high levels of light in the intertidal zone and A. elegantissima that naturally lack symbionts (aposymbiotic), collected from nearby deep-shade habitats. Two-dimensional gel electrophoresis profiles of both steady-state and newly synthesized proteins were compared between the two types of animals using scanning densitometry and image analysis. Symbiotic and aposymbiotic animals share a majority of proteins; however, striking differences in several abundant proteins in steady-state profiles occur. Two proteins are unique to symbiotic animals, one at 32 kDa with an isoelectric point (pI) of 7.9 and another at 31 kDa, pI 6.3. Levels of six proteins with an apparent molecular mass of 25 kDa and pI values ranging from 4.8 to 5.5 are greatly enhanced in aposymbiotic animals. Furthermore, profiles of newly synthesized proteins from symbiotic animals contain a unique cluster of proteins ranging from 25 to 30 kDa and pI 6.6 to 6.9. These marked differences in protein profiles must be a reflection either of underlying differences in the regulation of gene expression or in post-translational modification of common proteins. Identifying the symbiosis-specific products present in A. elegantissima and identifying the inter-partner signaling and cues that result in differential expression will provide an insight into the understanding of these highly integrated associations.

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