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人λIII轻链可变区的血清学和化学分化

Serologic and chemical differentiation of human lambda III light chain variable regions.

作者信息

Eulitz M, Murphy C, Weiss D T, Solomon A

机构信息

Department of Medicine, University of Tennessee Medical Center, Knoxville 37920.

出版信息

J Immunol. 1991 May 1;146(9):3091-6.

PMID:1901892
Abstract

Human lambda L chains of a major V lambda subgroup, V lambda III, have been differentiated serologically and chemically into three V lambda III sub-subgroups designated V lambda IIIa, V lambda IIIb, and V lambda IIIc. Antisera prepared against lambda III Bence Jones proteins were obtained that recognized distinctive V lambda III-related epitopes expressed by monoclonal lambda III L chains. After appropriate absorption, these reagents were rendered specific for three distinct populations of lambda III proteins--lambda IIIa, lambda IIIb, and lambda IIIc. The antisera were used in comparative immunodiffusion analyses of 28 monoclonal lambda III L chains, 10 of which were classified as lambda IIIa, 4 as lambda IIIb, and 14 as lambda IIIc. The isotypic nature of the three lambda III sub-subgroups was demonstrated serologically through analyses of lambda-chains derived from the serum IgG molecules of normal individuals. The amino acid sequences of five serologically classified lambda III chains, which included members of the three V lambda III sub-subgroups, had been previously determined. This information, in addition to our establishment of the complete (or virtually complete) V region sequence of 15 and the partial sequence of eight other lambda IIIa, lambda IIIb, and lambda IIIc proteins, made it possible to correlate chemical data with serologic classification. Proteins within each of the three serologically-classified lambda III sub-subgroups typically possessed a high degree (approximately 83%) of intra-sub-subgroup sequence homology that included both framework and complementarity determining region residues. Furthermore, within the framework and complementarity determining regions, sub-subgroup-specific residues were identified. Taken together, these data reveal that the human V lambda III genome consists of (at least) three distinct V lambda IIIa, V lambda IIIb, and V lambda IIIc germline genes that encode for lambda IIIa, lambda IIIb, and lambda IIIc L chains, respectively.

摘要

主要Vλ亚群VλIII的人λ轻链已通过血清学和化学方法分化为三个VλIII亚亚群,分别命名为VλIIIa、VλIIIb和VλIIIc。制备了针对λIII本-周蛋白的抗血清,该抗血清可识别由单克隆λIII轻链表达的独特的VλIII相关表位。经过适当吸收后,这些试剂对三种不同的λIII蛋白群体(λIIIa、λIIIb和λIIIc)具有特异性。这些抗血清用于对28条单克隆λIII轻链进行比较免疫扩散分析,其中10条被归类为λIIIa,4条为λIIIb,14条为λIIIc。通过分析来自正常个体血清IgG分子的λ链,血清学证明了三个λIII亚亚群的同种型性质。先前已确定了五条经血清学分类的λIII链的氨基酸序列,其中包括三个VλIII亚亚群的成员。这些信息,加上我们确定的15条λIIIa、λIIIb和λIIIc蛋白的完整(或几乎完整)V区序列以及另外8条的部分序列,使得将化学数据与血清学分类相关联成为可能。在血清学分类的三个λIII亚亚群中的每一个亚亚群内的蛋白质通常具有高度(约83%)的亚亚群内序列同源性,包括框架区和互补决定区残基。此外,在框架区和互补决定区内,鉴定出了亚亚群特异性残基。综上所述,这些数据表明人类VλIII基因组由(至少)三个不同的种系基因VλIIIa、VλIIIb和VλIIIc组成,它们分别编码λIIIa、λIIIb和λIIIc轻链。

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