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FS Chen PE Di Cesare AA Kale JF Lee VH Frankel SA Stuchin JD Zuckerman 《Canadian Metallurgical Quarterly》1998,13(8):867-873
We have developed a computer program for the rapid assessment of the primary structure differences between a protein of unknown sequence and a homologous known protein. Both proteins are reduced, alkylated, and digested with the same hydrolytic agent. The unfractionated peptide mixtures are submitted to automatic sequence analysis. Based on the knowledge of the reference sequence, the program utilizes the analysis data to identify all the potential peptides present in the two mixtures, determining their primary structure, homology degree, and molecular weight calculated both as integer MH+ and average mass variables. These fingerprints allow the user to easily identify the structural differences between the two proteins and clarify possible doubts by a mass spectrometric analysis of the two mixtures. In order to verify the utility of the program, we provide an application example using the already reported data of two homologous proteins. 相似文献
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JM Ding GF Buchanan SA Tischkau D Chen L Kuriashkina LE Faiman JM Alster PS McPherson KP Campbell MU Gillette 《Canadian Metallurgical Quarterly》1998,394(6691):381-384
Circadian clocks are complex biochemical systems that cycle with a period of approximately 24 hours. They integrate temporal information regarding phasing of the solar cycle, and adjust their phase so as to synchronize an organism's internal state to the local environmental day and night. Nocturnal light is the dominant regulator of this entrainment. In mammals, information about nocturnal light is transmitted by glutamate released from retinal projections to the circadian clock in the suprachiasmatic nucleus of the hypothalamus. Clock resetting requires the activation of ionotropic glutamate receptors, which mediate Ca2+ influx. The response induced by such activation depends on the clock's temporal state: during early night it delays the clock phase, whereas in late night the clock phase is advanced. To investigate this differential response, we sought signalling elements that contribute solely to phase delay. We analysed intracellular calcium-channel ryanodine receptors, which mediate coupled Ca2+ signalling. Depletion of intracellular Ca2+ stores during early night blocked the effects of glutamate. Activators of ryanodine receptors induced phase resetting only in early night; inhibitors selectively blocked delays induced by light and glutamate. These findings implicate the release of intracellular Ca2+ through ryanodine receptors in the light-induced phase delay of the circadian clock restricted to the early night. 相似文献
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一、前言在中子活化分析中通常采用密封石英瓶汞标准。然而,它并不是一种理想的辐照汞标准,还存在一些问题有待解决。据文献[1]报道首次将流基联在棉花的大分子链上,制成了用来吸附宫集有机汞、无机汞的巯基纤维。据此,我们制备了一种新的用于反应堆中子 相似文献
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