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与人类中性粒细胞NADPH氧化酶相关的47 kDa磷蛋白的纯化

Purification of the 47 kDa phosphoprotein associated with the NADPH oxidase of human neutrophils.

作者信息

Teahan C G, Totty N, Casimir C M, Segal A W

机构信息

Department of Medicine, University College London, U.K.

出版信息

Biochem J. 1990 Apr 15;267(2):485-9. doi: 10.1042/bj2670485.

Abstract

A 47 kDa protein in the cytosol of phagocytic cells becomes heavily phosphorylated and translocates to the cell membrane upon stimulation. This protein was isolated from the cytosol of human neutrophils by chromatography on ion-exchange and hydroxyapatite resins. Polyclonal antibodies to this protein demonstrated that it was present in the neutrophils of two patients with X-linked chronic granulomatous disease (CGD) but not in those of three patients with the autosomal recessive pattern of inheritance. A sequence of amino acids was determined from a tryptic peptide of this protein: Glu-Met-Phe-Pro-Ile-Glu-Ala-Gly-Ala-Ile-Asn-Xaa-Glu. This served to establish that the phosphoprotein isolated here is the same as a protein of a similar molecular mass identified by other workers. These studies confirm the involvement of this 47 kDa phosphoprotein in the molecular pathology of autosomal recessive CGD and describe a method for the purification of the native protein.

摘要

吞噬细胞胞质溶胶中的一种47 kDa蛋白在受到刺激后会发生大量磷酸化并转位至细胞膜。该蛋白通过离子交换和羟基磷灰石树脂层析从人中性粒细胞的胞质溶胶中分离出来。针对该蛋白的多克隆抗体表明,它存在于两名X连锁慢性肉芽肿病(CGD)患者的中性粒细胞中,但不存在于三名具有常染色体隐性遗传模式患者的中性粒细胞中。从该蛋白的胰蛋白酶肽段中确定了一段氨基酸序列:Glu-Met-Phe-Pro-Ile-Glu-Ala-Gly-Ala-Ile-Asn-Xaa-Glu。这有助于确定此处分离的磷蛋白与其他研究人员鉴定的分子量相似的蛋白相同。这些研究证实了这种47 kDa磷蛋白参与常染色体隐性CGD的分子病理学,并描述了一种纯化天然蛋白的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3ebd/1131315/ac245de51d39/biochemj00185-0202-a.jpg

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