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Single-Strand DNA Binding Proteins01:03

Single-Strand DNA Binding Proteins

13.7K
For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
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Leaky Scanning02:28

Leaky Scanning

5.0K
During most eukaryotic translation processes, the small 40S ribosome subunit scans an mRNA from its 5' end until it encounters the first start AUG codon. The large 60S ribosomal subunit then joins the smaller one to initiate protein synthesis. The location of the translation initiation is largely determined by the nucleotides near the start codon as there may be multiple translation initiation sites present on the mRNA.  Marilyn Kozak discovered that the sequence RCCAUGG (where R...
5.0K
Cis-regulatory Sequences02:02

Cis-regulatory Sequences

9.5K
Cis-regulatory sequences are short fragments of non-coding DNA that are present on the same chromosomes as the genes that they regulate. These fragments serve as binding sites for transcriptional regulators, proteins that are responsible for controlling gene transcription and differential gene expression across cell types in eukaryotes. Cis-regulatory sequences can be close to the gene of interest or thousands of bases away in the DNA sequence; however, those sequences that are further away are...
9.5K
RNA Splicing01:32

RNA Splicing

55.7K
Splicing is the process by which eukaryotic RNA is edited before its translation into protein. The RNA strand transcribed from eukaryotic DNA is called the primary transcript. The primary transcripts that become mRNAs are called precursor messenger RNAs (pre-mRNAs). Eukaryotic pre-mRNA contains alternating sequences of exons and introns. Exons are nucleotide sequences that code for proteins, whereas introns are the non-coding regions. In RNA splicing, introns are removed and exons are bonded...
55.7K
Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

2.3K
Nuclear protein sorting regulates nucleus composition and gene expression, crucial for determining the fate of a eukaryotic cell. Hence, the entry and exit of molecules across the nuclear envelope is a tightly controlled process. Nuclear protein sorting can be inhibited by one of the following ways: 1) masking cargo signal sequences, 2) modifying the nuclear receptor's affinity for cargo, 3) controlling the nuclear pore size, 4) retaining the cargo during its transit to the cytosol or the...
2.3K
Signal Sequences and Sorting Receptors01:41

Signal Sequences and Sorting Receptors

5.1K
Signal sequences are short amino acid sequences that guide newly synthesized proteins to their proper location within the cell. Classical signal sequences are fifteen to sixty amino acids long and present at the N-terminus of a polypeptide chain. Each signal sequence has a conserved segment of basic residues towards their N terminus, a hydrophobic core, and a C-terminus rich in polar residues. The C-terminus also contains a signal cleavage site and features a -3 -1 sequence motif. The -3-1...
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相关实验视频

Updated: May 9, 2025

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity
09:16

In Vitro Directed Evolution of a Restriction Endonuclease with More Stringent Specificity

Published on: March 25, 2020

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Nsp15的裂纹序列特异性 Nsp15的裂纹序列特异性

John V McGuire1, Scott Horowitz1

  • 1Department of Chemistry & Biochemistry, Knoebel Institute for Healthy Aging, University of Denver, Denver, CO.

RNA biology
|May 6, 2025
PubMed
概括

作为SARS-CoV-2酶的NSP15,在RNA分裂过程中的第一个二核酸位上显示出对尿素的偏好. 结构分析表明,这种特异性受到RNA序列附近相互作用的影响.

科学领域:

  • 病毒学 病毒学
  • 分子生物学分子生物学
  • 结构生物学 结构生物学

背景情况:

  • Nsp15是一种EndoU核酶,对SARS-CoV-2免疫逃避至关重要.
  • 了解NSP15的序列特异性对于抗病毒策略至关重要.
  • 之前的研究在完全确定NSP15序列特异性方面遇到了挑战.

研究的目的:

  • 系统地测量SARS-CoV-2 Nsp15酶的序列特异性.
  • 调查Nsp15的RNA分裂偏好背后的结构基础.

主要方法:

  • 采用了一种系统方法来测试Nsp15裂变活性的所有16种可能的二核酸序列.
  • 使用AlphaFold3预测来分析控制NSP15特异性的结构相互作用.
  • 进行了分离试验,以确定Nsp15的序列偏好.

主要成果:

  • 在第一个二核酸位上,NSP15显然更喜欢尿素 (U).
  • 第二个二核酸位的特异性有所不同.
  • 结构分析揭示了对二核酸序列和与二核酸本身的关键3'相互作用,与观察到的裂变特异性相关.

结论:

关键词:
阿尔法折叠是什么意思阿尔法折叠体核糖核酶的使用方法非结构蛋白 15 非结构蛋白 15在 Nsp15 中使用.降解RNA的降解RNA的降解这就是SARS-CoV-2病毒.序列的特异性 序列的特异性

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  • 该研究阐明了NSP15的序列特异性,突出了U在第一个位置的偏好.
  • 来自AlphaFold3的结构洞察力为理解这些酶偏好提供了基础.
  • 这种对NSP15功能的详细理解可以为针对SARS-CoV-2的向抗病毒疗法的开发提供信息.