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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
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Protein glycosylation starts in the ER lumen and continues in the Golgi apparatus. Glycosyltransferases catalyze the addition of sugar molecules or glycosylation of proteins. Usually, these enzymes add sugars to the hydroxyl groups of selected serine or threonine residues to form O-linked glycans or the amino groups of asparagine residues to form N-linked glycans. Different positions on the same polypeptide chain can contain differently linked glycans.
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Glycosylation, the most common post-translational modification for proteins, serves diverse functions. Adding sugars to proteins makes the proteins more resistant to proteolytic digestion. Glycosylated proteins can act as markers and receptors to promote cell-cell adhesion. Additionally, they have many essential quality control functions in the cell, such as correct protein folding and facilitating transport of misfolded proteins to the cytosol, which can be degraded.
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Visualizing Intracellular Sialylation with Click Chemistry and Expansion Microscopy
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生物合成甘油标签

Victoria M Marando1, Daria E Kim1, Phillip J Calabretta1,2

  • 1Department of Chemistry, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.

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概括

研究人员开发了一种使用细胞酶标记甘氨酸的新方法. 这种新的探测器可以选择性地标记细菌中的阿拉比诺,

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科学领域:

  • 碳水化合物化学
  • 化学生物学
  • 微生物学

背景情况:

  • 甘氨酸是重要的生物分子, 但由于有限的化学工具在细胞中研究它们是具有挑战性的.
  • 由于它们的结构相似,对于蛋白质等生物大分子的现有方法并不直接适用于甘氨酸.

研究的目的:

  • 开发一种可通用的化学选择性甘氨酸修饰策略.
  • 创建一个用于探测细胞环境中的甘氨酸结构和功能的工具.

主要方法:

  • 设计的生物对角探针作为糖转移酶的基质替代物.
  • 合成并测试了d-arabinofuranose (d-Araf) 探针用于菌根细胞壁.
  • 用于选择性标记的葡萄糖转移酶.

主要成果:

  • 开发了第一个用于选择性标记含有阿拉比诺糖的探针.
  • 证明了探测器在真菌生长过程中揭示不对称的d-Araf分布的能力.
  • 显示了在巨中检测菌根的潜力.

结论:

  • 这种方法为创建各种单糖的化学选择性标签剂提供了一个新的平台.
  • 通过d-Araf探测器,可以了解菌根细胞壁的组成和动态.
  • 开发的方法在病原体检测中具有潜在的应用.