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相关概念视频

Overview of Secretory Vesicles01:33

Overview of Secretory Vesicles

Secretory vesicles, also known as dense core vesicles (DCVs), are membrane-bound vesicles that transport secretory proteins, such as hormones or neurotransmitters. Regulated secretory vesicles transport proteins from the trans-Golgi network to the exterior of the cell. Proteins present in regulated secretory vesicles are required to be rapidly exocytosed in large amounts upon a specific stimulus.
Various proteins regulate the aggregation of molecules inside the secretory vesicles. Chromogranins...
Regulation of Nuclear Protein Sorting01:45

Regulation of Nuclear Protein Sorting

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...
SNAREs and Membrane Fusion01:43

SNAREs and Membrane Fusion

Once a transport vesicle has recognized its target organelle, the vesicular membrane needs to fuse with the target membrane to unload the cargo. Transmembrane proteins called SNAREs present on organelle membranes and their vesicles, mediate vesicle fusion.
SNAREs exist in pairs that symmetrically interact and catalyze the fusion of the lipid bilayers in vesicle and target organelle. v-SNARE in the vesicle membrane are single polypeptide chains that bind to a complementary t-SNARE, composed of 2...
Bacterial Protein Maturation01:26

Bacterial Protein Maturation

Bacterial protein maturation is a tightly regulated process that ensures newly synthesized polypeptides achieve correct functional conformations. This maturation involves a series of modifications, folding events, and quality control steps, often assisted by specialized chaperone proteins.N-Terminal ModificationsThe maturation of bacterial polypeptides begins cotranslationally as the polypeptide exits the ribosome. The first amino acid, N-formylmethionine (fMet), is typically modified at the...
Translational Regulation01:29

Translational Regulation

Translational regulation in prokaryotes ensures efficient protein synthesis by controlling ribosome access to mRNA. This regulation is mediated by secondary RNA structures, including translational riboswitches, RNA thermometers, and small RNAs (sRNAs), which respond to intracellular and environmental signals to modulate gene expression.Translational RiboswitchesRiboswitches in the leader region of mRNAs can regulate translation by altering the accessibility of the Shine-Dalgarno (SD) sequence,...
Gene Regulation During Sporulation01:17

Gene Regulation During Sporulation

Sporulation is a complex developmental process that allows certain Gram-positive bacteria, such as Bacillus subtilis and Clostridium species, to survive extreme environmental conditions. This process is tightly regulated by a series of signaling cascades and transcriptional controls, ensuring the formation of a highly resistant endospore.Sporulation is triggered by unfavorable conditions, such as nutrient depletion, and is governed by a phosphorelay system. One of the sensor kinases, such as...

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相关实验视频

Updated: Jul 7, 2026

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides
09:42

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides

Published on: June 19, 2012

酵母极性蛋白Sro7的结构揭示了一个SNARE调节机制.

Douglas A Hattendorf1, Anna Andreeva, Akanksha Gangar

  • 1Department of Structural Biology, Stanford University School of Medicine, 299 Campus Drive West, Stanford, California 94305-5126, USA.

Nature
|March 30, 2007
PubMed
概括
此摘要是机器生成的。

致命的巨型幼虫蛋白通过与SNARE蛋白相互作用来调节极化异细胞分裂. 这是Sro7蛋白质.

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Efficient Sporulation of Saccharomyces cerevisiae in a 96 Multiwell Format
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Efficient Sporulation of Saccharomyces cerevisiae in a 96 Multiwell Format

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Combining X-Ray Crystallography with Small Angle X-Ray Scattering to Model Unstructured Regions of Nsa1 from S. Cerevisiae
09:15

Combining X-Ray Crystallography with Small Angle X-Ray Scattering to Model Unstructured Regions of Nsa1 from S. Cerevisiae

Published on: January 10, 2018

相关实验视频

Last Updated: Jul 7, 2026

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides
09:42

Using SecM Arrest Sequence as a Tool to Isolate Ribosome Bound Polypeptides

Published on: June 19, 2012

Efficient Sporulation of Saccharomyces cerevisiae in a 96 Multiwell Format
08:54

Efficient Sporulation of Saccharomyces cerevisiae in a 96 Multiwell Format

Published on: September 17, 2016

Combining X-Ray Crystallography with Small Angle X-Ray Scattering to Model Unstructured Regions of Nsa1 from S. Cerevisiae
09:15

Combining X-Ray Crystallography with Small Angle X-Ray Scattering to Model Unstructured Regions of Nsa1 from S. Cerevisiae

Published on: January 10, 2018

科学领域:

  • 细胞生物学 细胞生物学
  • 分子生物学分子生物学
  • 生物化学 生物化学

背景情况:

  • 极化外细胞分裂对细胞功能至关重要,需要精确的协调.
  • 分泌囊泡融合依赖于SNARE复合体,涉及R-SNARE和血膜Qa,Qb,Qc SNARE蛋白质.
  • 致命巨 (Lgl) 家族的蛋白质,包括Sro7,tomosyn和Lgl,是这个过程的关键调节者.

研究的目的:

  • 阐明Sro7在极化表细胞突变中的结构基础和调节机制.
  • 研究Sro7和SNARE蛋白之间的相互作用,特别是Sec9.
  • 了解Sro7尾域在调节外细胞形成中的作用.

主要方法:

  • 确定Sro7.7的晶体结构.
  • 通过删除突变体对Sro7-Sec9相互作用的分析.
  • Lgl家族蛋白质的序列对齐.

主要成果:

  • Sro7的晶体结构显示了两个WD40β螺旋和一个调节尾巴.
  • 删除Sro7尾部增强了Sec9的Qbc SNARE区域的结合,抑制了SNARE复合体的组合.
  • 通过它的尾部和N端域,Sro7与Sec9相互作用,这表明了全调节.

结论:

  • Sro7作为极化细胞外的全调节剂.
  • Sro7的尾部域在调节SNARE复合体形成方面发挥着至关重要的作用.
  • 像tomosyn这样的同类可能具有类似的调节机制,涉及尾部域.