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MHC class I molecules function to present peptides eight to ten residues long to the immune system. These peptides originate primarily from a cytosolic pool of proteins through the actions of proteasomes, and are transported into the endoplasmic reticulum, where they assemble with nascent class I molecules. Most peptides are generated from proteins that are apparently metabolically stable. To explain this, we previously proposed that peptides arise from proteasomal degradation of defective ribosomal products (DRiPs). DRiPs are polypeptides that never attain native structure owing to errors in translation or post-translational processes necessary for proper protein folding. Here we show, first, that DRiPs constitute upwards of 30% of newly synthesized proteins as determined in a variety of cell types; second, that at least some DRiPs represent ubiquitinated proteins; and last, that ubiquitinated DRiPs are formed from human immunodeficiency virus Gag polyprotein, a long-lived viral protein that serves as a source of antigenic peptides.  相似文献   
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Effects of multiplicatioe noise in transient laser intensity are investigated theoretically. Analytic solutions are calculated through a reduced Fokker-Planck equation and the results with different pump parameters are discussed.  相似文献   
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A C3Cl-type(bcc)-semi-infinite ferrimagnet with a single-ion uniaxial anisotropy and a magnetic impurity layer is considered through combining Green‘s function theory with the transfer-mairx method.The effect of the anisotropy term and the impurity layer on surface spin wave specirum is discussed.The influence of the impurity layer‘s distance from the surface or surface spin woves is also concerned.  相似文献   
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