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毛细胞型抗酒石酸酸性磷酸酶的异质性

Heterogeneity of hairy cell tartrate-resistant acid phosphatase.

作者信息

Janckila A J, Latham M D, Lam K W, Chow K C, Li C Y, Yam L T

机构信息

Medical Service, Department of Veterans Affairs Medical Center, Louisville, KY 40206.

出版信息

Clin Biochem. 1992 Dec;25(6):437-43. doi: 10.1016/0009-9120(92)90075-4.

Abstract

The human nonerythrocytic acid phosphatases (AcP) are composed of seven distinct activity bands in nondenaturing polyacrylamide gel electrophoresis (PAGE) when stained using either 1-naphthyl phosphate or naphthol ASBI phosphate as substrate. They are numbered 0, 1, 2, 3, 3b, 4, and 5 according to their increasing mobility toward the cathode in acidic conditions. Of these, only the most cationic "band 5" is tartrate resistant (TRAcP). When naphthol ASBI phosphate is used as substrate, AcP activity can also be stained in situ. In the presence of tartrate, activity remains strong in the hairy cells (HC) of hairy cell leukemia (HCL). Thus, the TRAcP stain has remained a reliable marker for HC. To investigate the function of TRAcP in HC, we purified two isoforms of TRAcP from HCL spleen tissue and found them to have similar substrate specificities and inhibitor sensitivities. In this report, we describe in detail the methods for TRAcP purification and compare some of the structural properties of the two isoforms to reinforce the concept that human TRAcP is a heterogeneous group of related enzymes. Band 5 represented only 15-20% of the total TRAcP extracted from HCL spleen. The remaining 80% of TRAcP hydrolyzed p-nitrophenyl phosphate but not naphthol ASBI phosphate and was not detectable in acidic, nondenaturing PAGE gels. Band 5 was solubilized from tissue using 500 mmol/L NaCl after previous extraction with 0.5% (v/v) NP-40 removed most other AcP and TRAcP activity.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

当使用1-萘基磷酸酯或萘酚ASBI磷酸酯作为底物进行染色时,人类非红细胞酸性磷酸酶(AcP)在非变性聚丙烯酰胺凝胶电泳(PAGE)中由七条不同的活性带组成。根据它们在酸性条件下向阴极迁移率的增加,将它们编号为0、1、2、3、3b、4和5。其中,只有最具阳离子性的“带5”对酒石酸具有抗性(TRAcP)。当使用萘酚ASBI磷酸酯作为底物时,AcP活性也可以原位染色。在酒石酸存在的情况下,毛细胞白血病(HCL)的毛细胞(HC)中的活性仍然很强。因此,TRAcP染色一直是HC的可靠标志物。为了研究TRAcP在HC中的功能,我们从HCL脾脏组织中纯化了两种TRAcP同工型,发现它们具有相似的底物特异性和抑制剂敏感性。在本报告中,我们详细描述了TRAcP纯化的方法,并比较了两种同工型的一些结构特性,以强化人类TRAcP是一组相关酶的异质群体这一概念。带5仅占从HCL脾脏中提取的总TRAcP的15%-20%。其余80%的TRAcP水解对硝基苯磷酸酯,但不水解萘酚ASBI磷酸酯,并且在酸性非变性PAGE凝胶中无法检测到。在用0.5%(v/v)NP-40预先提取去除了大多数其他AcP和TRAcP活性后,使用500 mmol/L NaCl从组织中溶解带5。(摘要截短于250字)

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