首页> 美国卫生研究院文献>The Journal of Physiology >Specific motifs in the external loops of connexin proteins can determine gap junction formation between chick heart myocytes.
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Specific motifs in the external loops of connexin proteins can determine gap junction formation between chick heart myocytes.

机译:连接蛋白蛋白外环中的特定基序可以决定鸡心肌细胞之间的间隙连接形成。

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摘要

1. Gap junction formation was compared in the absence and presence of small peptides containing extracellular loop sequences of gap junction (connexin) proteins by measuring the time taken for pairs of spontaneously beating embryonic chick heart myoballs to synchronize beat rates. Test peptides were derived from connexin 32. Non-homologous peptides were used as controls. Control pairs took 42 +/- 0.5 min (mean +/- S.E.M.; n = 1088) to synchronize. 2. Connexins 32 and 43, but not 26, were detected in gap junction plaques. The density and distribution of connexin immunolabelling varied between myoballs. 3. Peptides containing conserved motifs from extracellular loops 1 and 2 delayed gap junction formation. The steep portion of the dose-response relation lay between 30 and 300 microM peptide. 4. In loop 1, the conserved motifs QPG and SHVR were identified as being involved in junction formation. In loop 2, the conserved SRPTEK motif was important. The ability of peptides containing the SRPTEK motif to interfere with the formation of gap junctions was enhanced by amino acids from the putative membrane-spanning region. 5. Peptides from loop 1 and loop 2 were equivalently effective; there was no synergism between them. 6. The inclusion of conserved cysteines in test peptides did not make them more effective in the competition assay.
机译:1.通过测量成对自发跳动的雏鸡心脏心肌对同步搏动速率所花费的时间,比较了在不存在间隙连接(连接蛋白)蛋白胞外环序列的小肽存在与否的情况下,间隙连接的形成情况。测试肽衍生自连接蛋白32。非同源肽用作对照。对照对花费42 +/- 0.5分钟(平均+/- S.E.M.; n = 1088)进行同步。 2.在缝隙连接斑块中检测到连接蛋白32和43,但未检测到26。连接蛋白免疫标记的密度和分布在肌球之间变化。 3.含有来自细胞外环1和2的保守基序的肽延迟了间隙连接的形成。剂量反应关系的陡峭部分位于30和300 microM肽之间。 4.在循环1中,保守的基序QPG和SHVR被鉴定为参与结形成。在循环2中,保守的SRPTEK基序很重要。推定的跨膜区域的氨基酸增强了包含SRPTEK基序的肽干扰间隙连接形成的能力。 5.来自环1和环2的肽等效有效;他们之间没有协同作用。 6.在测试肽中包含保守的半胱氨酸并没有使其在竞争测定中更有效。

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