小鼠组织相容性抗原H-2Kd和H-2Db上存在三种碳水化合物辅基的证据。 - Suppr

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超能文献

Evidence for three carbohydrate prosthetic groups on mouse histocompatibility antigens H-2Kd and H-2Db.

作者信息

Kimball E S, Maloy W L, Coligan J E

出版信息

Mol Immunol. 1981 Jul;18(7):677-80. doi: 10.1016/0161-5890(81)90039-0.

DOI:10.1016/0161-5890(81)90039-0

PMID:6170885

Abstract

摘要

相似文献

Evidence for three carbohydrate prosthetic groups on mouse histocompatibility antigens H-2Kd and H-2Db.小鼠组织相容性抗原H-2Kd和H-2Db上存在三种碳水化合物辅基的证据。

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Structural studies on H-2Db and H-2Kd molecules indicate that murine major histocompatibility b and d haplotype alloantigens share structural features.对H-2Db和H-2Kd分子的结构研究表明，小鼠主要组织相容性b和d单倍型同种异体抗原具有共同的结构特征。

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[Synthesis and immunochemical study of the antigenic determinant of the H-2Db molecule of the murine major histocompatibility complex].[小鼠主要组织相容性复合体H-2Db分子抗原决定簇的合成及免疫化学研究]

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Intramolecular organization of Class I H-2 MHC antigens; localization of the alloantigenic determinants and the beta 2 m binding site to different regions of the H-2 Kb glycoprotein.I类H-2 MHC抗原的分子内组织；同种异型抗原决定簇和β2m结合位点在H-2 Kb糖蛋白不同区域的定位。

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Subunit structure, cell surface orientation, and partial amino-acid sequences of murine histocompatibility antigens.小鼠组织相容性抗原的亚基结构、细胞表面定位及部分氨基酸序列

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The structural-genetic relationships of the H-2K and H-2D products of the mouse major histocompatibility complex.

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Association of mouse major histocompatibility and Rauscher murine leukaemia virus envelope glycoprotein antigens on leukaemia cells and their recognition by syngeneic virus-immune-cytotoxic T-lymphocytes.小鼠主要组织相容性复合体与劳氏鼠白血病病毒包膜糖蛋白抗原在白血病细胞上的关联以及同基因病毒免疫细胞毒性T淋巴细胞对它们的识别。

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Amino acid sequence of the cytoplasmic segment of the h-2Kd (H2.31) murine major histocompatibility antigen.h-2Kd（H2.31）小鼠主要组织相容性抗原细胞质区段的氨基酸序列。

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Variable binding affinities of listeriolysin O peptides for the H-2Kd class I molecule.李斯特菌溶血素O肽与H-2Kd I类分子的可变结合亲和力。

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引用本文的文献

Primary structure of the H-2Db alloantigen. II. Additional amino acid sequence information, localization of a third site of glycosylation and evidence for K and D region specific sequences.H-2Db同种异体抗原的一级结构。II. 额外的氨基酸序列信息、第三个糖基化位点的定位以及K和D区域特异性序列的证据。

Immunogenetics. 1982;16(1):11-22. doi: 10.1007/BF00364438.

The complete amino acid sequence of the murine transplantation antigen H-2Db as deduced by molecular cloning.通过分子克隆推导得出的小鼠移植抗原H-2Db的完整氨基酸序列。

Immunogenetics. 1982;16(1):1-9. doi: 10.1007/BF00364437.

Identification of a second class I antigen controlled by the K end of the H-2 complex and its selective cellular expression.鉴定由H-2复合体K端控制的第二类I类抗原及其选择性细胞表达。

Proc Natl Acad Sci U S A. 1983 Mar;80(5):1445-8. doi: 10.1073/pnas.80.5.1445.

Serological and immunochemical analysis of H-2 class I molecules encoded by the Db region.对由Db区域编码的H-2 I类分子进行血清学和免疫化学分析。

Immunogenetics. 1984;20(3):341-5. doi: 10.1007/BF00364215.

Expression of H-2Db on the cell surface in the absence of detectable beta 2 microglobulin.在未检测到β2微球蛋白的情况下，H-2Db在细胞表面的表达。

J Exp Med. 1984 Jul 1;160(1):317-22. doi: 10.1084/jem.160.1.317.

Analysis of human class I antigens by two-dimensional gel electrophoresis. I. Polymorphism, evidence for additional (non-HLA-A, B, C) gene products, and identification of variant HLA-A, B antigens.通过二维凝胶电泳分析人类I类抗原。I. 多态性、额外（非HLA-A、B、C）基因产物的证据以及变异HLA-A、B抗原的鉴定。

Immunogenetics. 1983;17(4):333-56. doi: 10.1007/BF00372454.

Structure of crossreactive human histocompatibility antigens HLA-A28 and HLA-A2: possible implications for the generation of HLA polymorphism.交叉反应性人类组织相容性抗原HLA - A28和HLA - A2的结构：对HLA多态性产生的可能影响

Proc Natl Acad Sci U S A. 1982 Jun;79(12):3813-7. doi: 10.1073/pnas.79.12.3813.

Molecular analysis of an EL4 cell line that expresses H-2Db but not H-2Kb or beta 2-microglobulin.对一个表达H-2Db但不表达H-2Kb或β2-微球蛋白的EL4细胞系进行分子分析。

Proc Natl Acad Sci U S A. 1985 May;82(9):2950-4. doi: 10.1073/pnas.82.9.2950.

Carbohydrate moieties of rat MHC class I antigens.大鼠主要组织相容性复合体I类抗原的碳水化合物部分

Immunogenetics. 1987;26(4-5):204-10. doi: 10.1007/BF00346513.

Comparison of rat MHC class I antigens by peptide mapping.通过肽图谱分析比较大鼠MHC I类抗原

Immunogenetics. 1987;25(1):35-46. doi: 10.1007/BF00768831.

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