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首页> 外文期刊>Angewandte Chemie >Design of Antisense (Complementary) Peptides as Selective Inhibitors of Cytokine Interleukin-1
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Design of Antisense (Complementary) Peptides as Selective Inhibitors of Cytokine Interleukin-1

机译:反义(互补)肽作为细胞因子白介素1的选择性抑制剂的设计

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摘要

Double-helical DMA comprises two complementary oligo-nucleotide chains Traditionally, one of these chains, the sense strand, defines the genetic code, whilst the complementary chain, the antisense strand, provides the means of propagating that code. However, the relationship between sense and anti-sense strands of DNA now appears to be more complex. In 1984 Blalock and Smith observed that antisense strand DNA was able to code for peptides, known as antisense peptides, which are the hydropathic complement of those sense peptides coded for in the normal way by sense strand DNA. Subsequently, evidence has been accumulating to suggest that antisense and corresponding sense peptides may interact specifically, with important biological consequences.
机译:双螺旋DMA包含两条互补的寡核苷酸链传统上,其中一条链(有义链)定义了遗传密码,而互补链(反义链)提供了传播该密码的方法。但是,DNA的有义链和反义链之间的关系现在似乎更加复杂。 1984年,Blalock和Smith观察到,反义链DNA能够编码称为反义肽的肽,这是正义链正常编码的那些有义肽的亲水互补。随后,越来越多的证据表明,反义和相应的有义肽可能特异性相互作用,具有重要的生物学后果。

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