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一种可中和I型人T细胞白血病/淋巴瘤病毒的人单克隆抗体表位的鉴定与合成

Identification and synthesis of the epitope for a human monoclonal antibody which can neutralize human T-cell leukemia/lymphotropic virus type I.

作者信息

Ralston S, Hoeprich P, Akita R

机构信息

Triton Biosciences, Inc., Alameda, California 94501.

出版信息

J Biol Chem. 1989 Oct 5;264(28):16343-6.

PMID:2476442
Abstract

A monoclonal antibody (mAb), designated 0.5 alpha, derived from a patient with adult T-cell leukemia was found previously to neutralize the human T-cell leukemia/lymphotropic type I (HTLV-I) virus in in vitro assays and bind to the major envelope glycoprotein (gp46) of HTLV-I (Matsushita, S., Guroff, M.R., Trepel, J., Crossman, J., Mitsuya, H., and Broder, S. (1986) Proc. Natl. Acad. Sci. U.S.A. 83, 2671-2676). We have designed experiments to determine the epitope for this mAb. Using simultaneous multiple peptide synthesis, we synthesized 481 overlapping octapeptides which corresponded to the sequence of gp46. We mapped the epitope for mAb 0.5 alpha to lie between residues 186 and 195 of gp46. This result was confirmed by independently synthesizing a peptide containing this epitope which bound specifically to mAb 0.5 alpha with an approximate Ka = 4 x 10(7) M-1. In addition, the peptide inhibited mAb 0.5 alpha binding to gp46 derived from T-cells infected with HTLV-I. This epitope containing peptide may facilitate understanding HTLV-1 infection of T-cells.

摘要

先前发现,从一名成人T细胞白血病患者体内获得的一种名为0.5α的单克隆抗体(mAb),在体外试验中可中和人T细胞白血病/淋巴瘤病毒I型(HTLV-I),并与HTLV-I的主要包膜糖蛋白(gp46)结合(松下,S.,古罗夫,M.R.,特雷佩尔,J.,克罗斯曼,J.,三津谷,H.,和布罗德,S.(1986年)《美国国家科学院院刊》83,2671 - 2676)。我们设计了实验来确定这种单克隆抗体的表位。利用同步多肽合成技术,我们合成了481个与gp46序列相对应的重叠八肽。我们将单克隆抗体0.5α的表位定位在gp46的第186位和第195位残基之间。通过独立合成包含该表位的肽段,以大约Ka = 4×10⁷ M⁻¹的亲和力特异性结合单克隆抗体0.5α,这一结果得到了证实。此外,该肽段抑制了单克隆抗体0.5α与感染HTLV-I的T细胞来源的gp46的结合。这种包含表位的肽段可能有助于理解HTLV-1对T细胞的感染。

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