1h87: Difference between revisions

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==Overview==
==Overview==
A neutral gadolinium complex, Gd-HPDO3A, is shown to be a good candidate, to use to obtain heavy-atom derivatives and solve macromolecular, structures using anomalous dispersion. Tetragonal crystals of a gadolinium, derivative of hen egg-white lysozyme were obtained by co-crystallization, using different concentrations of the complex. Diffraction data from three, derivative crystals (100, 50 and 10 mM) were collected to a resolution of, 1.7 A using Cu Kalpha radiation from a rotating anode. Two strong binding, sites of the gadolinium complex to the protein were located from the, gadolinium anomalous signal in both the 100 and 50 mM derivatives. A, single site is occupied in the 10 mM derivative. Phasing using the, anomalous signal at a single wavelength (SAD method) leads to an, electron-density map of high quality. The structure of the 100 mM, derivative has been refined. Two molecules of the gadolinium complex are, close together. Both molecules are located close to tryptophan residues., Four chloride ions were found. The exceptional quality of the SAD, electron-density map, only enhanced by solvent flattening, suggests that, single-wavelength anomalous scattering with the Gd-HPDO3A complex may be, sufficient to solve protein structures of high molecular weight by, synchrotron-radiation experiments, if not by laboratory experiments.
A neutral gadolinium complex, Gd-HPDO3A, is shown to be a good candidate to use to obtain heavy-atom derivatives and solve macromolecular structures using anomalous dispersion. Tetragonal crystals of a gadolinium derivative of hen egg-white lysozyme were obtained by co-crystallization using different concentrations of the complex. Diffraction data from three derivative crystals (100, 50 and 10 mM) were collected to a resolution of 1.7 A using Cu Kalpha radiation from a rotating anode. Two strong binding sites of the gadolinium complex to the protein were located from the gadolinium anomalous signal in both the 100 and 50 mM derivatives. A single site is occupied in the 10 mM derivative. Phasing using the anomalous signal at a single wavelength (SAD method) leads to an electron-density map of high quality. The structure of the 100 mM derivative has been refined. Two molecules of the gadolinium complex are close together. Both molecules are located close to tryptophan residues. Four chloride ions were found. The exceptional quality of the SAD electron-density map, only enhanced by solvent flattening, suggests that single-wavelength anomalous scattering with the Gd-HPDO3A complex may be sufficient to solve protein structures of high molecular weight by synchrotron-radiation experiments, if not by laboratory experiments.


==About this Structure==
==About this Structure==
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[[Category: o-glycosyl hydrolase]]
[[Category: o-glycosyl hydrolase]]


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