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Note: Herpes Simplex Virus Type 2 ICP47 Inhibits Human TAP but Not Mouse TAP

机译:注意:2型单纯疱疹病毒ICP47抑制人TAP但不能抑制小鼠TAP

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摘要

Herpes simplex virus serotype 1 (HSV-1) expresses an immediate-early protein, ICP47, that effectively blocks the major histocompatibility complex class I antigen presentation pathway. HSV-1 ICP47 (ICP47-1) binds with high affinity to the human transporter associated with antigen presentation (TAP) and blocks the binding of antigenic peptides. HSV type 2 (HSV-2) ICP47 (ICP47-2) has only 42% amino acid sequence identity with ICP47-1. Here, we compared the levels of inhibition of human and murine TAP, expressed in insect cell microsomes, by ICP47-1 and ICP47-2. Both proteins inhibited human TAP at similar concentrations, and the KD for ICP47-2 binding to human TAP was 4.8 × 10−8 M, virtually identical to that measured for ICP47-1 (5.2 × 10−8 M). There was some inhibition of murine TAP by both ICP47-2 and ICP47-1, but this inhibition was incomplete and only at ICP47 concentrations 50 to 100 times that required to inhibit human TAP. Lack of inhibition of murine TAP by ICP47-1 and ICP47-2 could be explained by an inability of both proteins to bind to murine TAP.
机译:单纯疱疹病毒血清型1(HSV-1)表达一种即刻早期蛋白ICP47,该蛋白有效阻断主要的组织相容性复合体I类抗原呈递途径。 HSV-1 ICP47(ICP47-1)与与抗原呈递(TAP)相关的人类转运蛋白高亲和力结合,并阻断抗原肽的结合。 HSV 2型(HSV-2)ICP47(ICP47-2)与ICP47-1仅具有42%的氨基酸序列同一性。在这里,我们比较了ICP47-1和ICP47-2在昆虫细胞微粒体中表达的人和鼠TAP的抑制水平。两种蛋白均以相似的浓度抑制人TAP,ICP47-2与人TAP结合的KD为4.8×10 -8 M,与ICP47-1的实测值相同(5.2×10 −8 M)。 ICP47-2和ICP47-1都对鼠类TAP有一定的抑制作用,但是这种抑制作用是不完全的,仅在ICP47浓度达到抑制人TAP所需浓度的50到100倍时才发生。 ICP47-1和ICP47-2对鼠类TAP的抑制作用不足可能是由于两种蛋白质均无法与鼠类TAP结合。

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