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[在人淋巴细胞多核糖体研究中合适的核糖核酸酶抑制剂的选择]

[Selection of appropriate ribonuclease inhibitors in the study of polysomes in human lymphocytes].

作者信息

Morozova E O, Blinov M N

出版信息

Vopr Med Khim. 1986 Mar-Apr;32(2):16-9.

PMID:3085343
Abstract

Polysome profiles are described for lymphocytes of donor peripheral blood treated with various inhibitors of RNAases. The most effective inhibitor was diethyl pyrocarbonate, which enabled to maintain high content of polysomes (up to 70%) in these cells. Ribosomes, treated with diethyl pyrocarbonate, exhibited functional activity in the puromycin test. A natural inhibitor of RNAases from liver tissue inhibited incompletely the enzymatic activity in lymphocytes. Heparin proved to be an inadequate inhibitor of RNAases in all the cells of lymphoid origin (lymphocytes from peripheral blood of donors and of the patients with chronic lympholeukosis, lymphocytes isolated from adenoids and spleen tissue); it induced disaggregation of polysomes and dissociation of ribosomes.

摘要

描述了用各种核糖核酸酶抑制剂处理的供体外周血淋巴细胞的多核糖体图谱。最有效的抑制剂是焦碳酸二乙酯,它能使这些细胞中多核糖体的含量保持在较高水平(高达70%)。用焦碳酸二乙酯处理的核糖体在嘌呤霉素试验中表现出功能活性。来自肝组织的核糖核酸酶天然抑制剂不能完全抑制淋巴细胞中的酶活性。肝素被证明在所有淋巴源性细胞(供体外周血淋巴细胞和慢性淋巴细胞白血病患者的淋巴细胞、从腺样体和脾组织分离的淋巴细胞)中都是一种不充分的核糖核酸酶抑制剂;它会导致多核糖体解聚和核糖体解离。

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