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[肽-蛋白质生物调节剂的起源与演化]

[Origin and evolution of peptide-protein bioregulators].

作者信息

Chipens G I, Freĭdlin I S, Skliarova S N

出版信息

Zh Evol Biokhim Fiziol. 1987 May-Jun;23(3):361-72.

PMID:3303757
Abstract

Possible evolutionary pathways of cellular regulatory systems are discussed. Analysis of animal evolution suggests that peptide and protein bioregulators emerged at an early stage during formation of biochemical systems in prokaryotic cells involving protein synthesis on ribosomes, the processes of exo- and endocytosis and limited proteolysis reactions. Primary autocrine bioregulators are compared with growth factors. Models for cellular bioregulation are discussed in which both cell receptors and peptide/protein ligands, primarily immunoglobins, act as prehormones. Their internalization and limited proteolysis can lead to formation of low-molecular peptides (tetines) acting as autocrine or paracrine bioregulators. Basing on the concept of biochemical universality, it is suggested that the effects of many growth factors, hormones, immunoglobulins, mono- and lymphokins are mediated by identical or similar (carrying the same signatures) fragments which are produced in cells due to limited proteolysis reactions and which are directly involved in activation of biochemical systems in these cells.

摘要

本文讨论了细胞调节系统可能的进化途径。对动物进化的分析表明,肽和蛋白质生物调节剂在原核细胞生化系统形成的早期阶段就已出现,这些生化系统涉及核糖体上的蛋白质合成、胞吞和胞吐过程以及有限的蛋白水解反应。将初级自分泌生物调节剂与生长因子进行了比较。讨论了细胞生物调节模型,其中细胞受体和肽/蛋白质配体(主要是免疫球蛋白)都作为前激素起作用。它们的内化和有限的蛋白水解可导致形成作为自分泌或旁分泌生物调节剂的低分子肽(tetines)。基于生化普遍性的概念,有人提出,许多生长因子、激素、免疫球蛋白、单克隆因子和淋巴因子的作用是由相同或相似(具有相同特征)的片段介导的,这些片段是细胞中由于有限的蛋白水解反应而产生的,并且直接参与这些细胞中生化系统的激活。

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