Binding of human ribosomal protein S16 with 18S rRNA fragment 1203-1236/1521-1698

被引:6
|
作者
Yanshina, D. D. [1 ]
Malygin, A. A. [1 ]
Karpova, G. G. [1 ]
机构
[1] Russian Acad Sci, Siberian Branch, Inst Chem Biol & Fundamental Med, Novosibirsk 630090, Russia
基金
俄罗斯基础研究基金会;
关键词
human ribosomal protein S16; 18S rRNA; footprinting; structure of 40S ribosomal subunit; RNA-protein interactions;
D O I
10.1134/S0026893307060106
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human ribosomal protein S16 is homologous to prokaryotic S9, which contacts the 16S rRNA region formed by helices H29, H30, H38-H41, and H43 by X-ray data. A study was made of the interaction of recombinant human S16 with an RNA transcript corresponding to human 18S rRNA region 1203-1236/1521-1698 (helices H28-30 and H41-43), homologous to the 16S rRNA region harboring part of the S9-binding site. S16 specifically bound to the transcript with an apparent dissociation constant of (1.3 +/- 0.1) . 10(-8) M at 20 degrees C. Enzymatic and chemical footprinting was used to identify the nucleotides whose accessibility for RNases and modifying chemical agents changes upon S16 binding. In the presence of S16, a substantially higher accessibility was observed for C1544 (internal loop of hairpin H41), C1618-U1622, C1629-A1634 (hairpin H42), C1521-C1523, U1530, C1532 (helix H30), C1645, C1646, and G1648 (base of hairpin H43) and an appreciably lower accessibility was observed for C1670-A1675 (hairpin H43). Many of the 16S rRNA nucleotides corresponding to the above 18S rRNA nucleotides tightly contact S9 residues in the bacterial 30S ribosomal subunit.
引用
收藏
页码:932 / 938
页数:7
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