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起始tRNA与真核起始因子eIF-2结合的调控。血红素控制的阻遏物对三元复合物形成动力学的影响。

Regulation of binding of initiator tRNA to eukaryotic initiation factor eIF-2. Effects of the haem-controlled repressor on the kinetics of ternary complex formation.

作者信息

Proud C G, Clemens M J, Pain V M

出版信息

FEBS Lett. 1982 Nov 8;148(2):214-20. doi: 10.1016/0014-5793(82)80810-7.

Abstract

Ternary complex formation was studied in reticulocyte lysate supernatants and using rat liver eukaryotic initiation factor-2 (eIF-2) preparations. Haem-deficiency reduced the rate of formation of ternary (Met-tRNAf . GTP . eIF-2) complexes by the eIF-2 in reticulocyte supernatants, the reduction being more marked when complex formation was assayed in the absence of GTP-regenerating capacity. Pretreatment with the haem-controlled repressor (HCR) reduced the rate of ternary complex formation by crude (liver) eIF-2. In contrast, complex formation by an almost homogeneous eIF-2 preparation was unaffected by HCR: sensitivity to HCR was however restored by a factor which catalyses exchange of guanine nucleotides bound to eIF-2.

摘要

在网织红细胞裂解物上清液中,并使用大鼠肝脏真核起始因子2(eIF-2)制剂研究了三元复合物的形成。血红素缺乏降低了网织红细胞上清液中eIF-2形成三元(Met-tRNAf·GTP·eIF-2)复合物的速率,当在缺乏GTP再生能力的情况下测定复合物形成时,这种降低更为明显。用血红素控制阻遏物(HCR)预处理降低了粗制(肝脏)eIF-2形成三元复合物的速率。相比之下,几乎纯一的eIF-2制剂形成复合物不受HCR影响:然而,与eIF-2结合的鸟嘌呤核苷酸催化交换的因子可恢复对HCR的敏感性。

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