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用于生成识别人类精子并在体外抑制受精能力的特异性Fab片段的组合噬菌体展示文库。

A combinatorial phage display library for the generation of specific Fab fragments recognizing human spermatozoa and inhibiting fertilizing capacity in vitro.

作者信息

Clayton R, Cooke I D, Partridge L J, Moore H D

机构信息

Department of Molecular Biology and Biotechnology, University of Sheffield, Sheffield, United Kingdom.

出版信息

Biol Reprod. 1998 Nov;59(5):1180-6. doi: 10.1095/biolreprod59.5.1180.

Abstract

To select a source of lymphocytes for the generation of an anti-sperm-biased combinatorial phage display library, venous blood was obtained from 34 vasovasostomy (vasectomy reversal) patients approximately 3 mo after surgery. Using a variety of immunoassays, serum was analyzed for antibodies against human spermatozoa, and a patient was selected on the basis of high titer of antibodies that recognized the equatorial region of the sperm head and inhibited sperm fertilizing capacity in vitro. Total RNA isolated from the stored lymphocytes of this individual was reversed transcribed, and gamma1 (Fd) region and kappa chains were amplified by polymerase chain reaction for the successful construction of an antibody phage display library. The library was panned against human spermatozoa to isolate sperm-specific phage that recognized the equatorial region of the sperm head. Three preparations of Fab were tested via the hamster egg penetration test. Each preparation significantly (p < 0. 005) inhibited sperm-egg binding and fusion, with one preparation (designated Fab-G) causing complete inhibition. Sequence analysis of the kappa light gene encoding Fab-G revealed a 93% homology with the light chain of human anti-human immunodeficiency virus gp120 p35 variable region. This technology may have a practical application in characterization of the immune response to spermatozoa and for the design of sperm-based contraceptive vaccines.

摘要

为了选择淋巴细胞来源以构建偏向抗精子的组合噬菌体展示文库,在术后约3个月从34例输精管吻合术(输精管复通术)患者获取静脉血。使用多种免疫测定法分析血清中针对人类精子的抗体,并根据识别精子头部赤道区且能在体外抑制精子受精能力的高滴度抗体来选择患者。从该个体储存的淋巴细胞中分离出的总RNA进行逆转录,通过聚合酶链反应扩增γ1(Fd)区和κ链,成功构建了抗体噬菌体展示文库。该文库与人类精子进行淘选,以分离识别精子头部赤道区的精子特异性噬菌体。通过仓鼠卵穿透试验对三种Fab制剂进行检测。每种制剂均显著(p<0.005)抑制精卵结合和融合,其中一种制剂(命名为Fab-G)导致完全抑制。对编码Fab-G的κ轻链基因进行序列分析,发现其与人类抗人类免疫缺陷病毒gp120 p35可变区轻链具有93%的同源性。该技术在精子免疫反应特征分析及基于精子的避孕疫苗设计方面可能具有实际应用价值。

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