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The flow of genetic information in cells from DNA to mRNA to protein is described by the central dogma, which states that genes specify the sequence of mRNAs, which in turn specify the sequence of amino acids making up all proteins. The decoding of one molecule to another is performed by specific proteins and RNAs. Because the information stored in DNA is so central to cellular function, it makes intuitive sense that the cell would make mRNA copies of this information for protein synthesis...
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While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.
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Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
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The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
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A Facile Protocol to Generate Site-Specifically Acetylated Proteins in Escherichia Coli
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最近在不断扩大的遗传密码方面取得的进展.

Michael L Pigula1, Peter G Schultz1

  • 1Department of Chemistry, Scripps Research, 10550 North Torrey Pines Road, La Jolla, CA 92037, United States.

Current opinion in chemical biology
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概括
此摘要是机器生成的。

科学家们正在将遗传密码扩展到超出20个标准氨基酸之外,使得能够创建具有增强功能的新型蛋白质. 这一突破允许精确的工程酶和生物疗法在生物系统.

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科学领域:

  • 合成生物学 合成生物学
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 生物学的核心教条传统上依赖于20种正规的氨基酸.
  • 规范性氨基酸的功能多样性有限,限制了蛋白质的能力.

研究的目的:

  • 审查最近在将非正规氨基酸 (ncAA) 纳入蛋白质方面的进展.
  • 突出ncAAs在蛋白质工程和治疗开发方面的潜力.

主要方法:

  • 使用独特的编码子将ncAA纳入特定站点.
  • 含有ncAA的蛋白质的高水平哺乳动物和真核生物表达系统.
  • 非α-氨基酸构建块的编码.

主要成果:

  • 数以百计具有新特性的ncAAs现在可以在特定位点内纳入蛋白质.
  • 在哺乳动物系统中成功地表达了ncAA修饰蛋白的高水平表达.
  • 在研究蛋白质功能和设计新生物疗法方面证明了实用性.

结论:

  • 用ncAAs扩展遗传密码为蛋白质科学提供了前所未有的机会.
  • 未来的研究方向包括进一步扩大ncAAs的曲目及其应用.
  • ncAA技术对促进生物技术和医学的发展具有重大前景.