相关实验视频

Updated: Feb 6, 2026

TurboID-Based Proximity Labeling for In Planta Identification of Protein-Protein Interaction Networks
07:02

TurboID-Based Proximity Labeling for In Planta Identification of Protein-Protein Interaction Networks

Published on: May 17, 2020

26.1K

在高光下,使用基于TurboID的近距离标记来识别Arabidopsis thaliana的叶片质体中的PsbS结合蛋白

Yuwei Jiao1,2, Yanhui Dou1,2, Lihua Wang1

  • 1Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences, Shanghai, China.

Frontiers in plant science
|February 5, 2026
PubMed
概括

光系统II子单元S (PsbS) 调节植物的光保护. 这项研究使用近距离标记来识别PsbS相互作用蛋白质,揭示新的合作伙伴,并建议PsbS通过构造变化而不是迁移来发挥作用.

关键词:
阿拉比多普西斯塔利亚纳.在NPQ中,NQQ是NQQ.PsbS 在线阅读光合作用 光合作用.接近性标签 蛋白质组学

更多相关视频

Using Changes in Leaf Transmission to Investigate Chloroplast Movement in Arabidopsis thaliana07:45

Using Changes in Leaf Transmission to Investigate Chloroplast Movement in Arabidopsis thaliana

Published on: July 14, 2021

2.7K
In Vivo Application of TurboID-based Proximity Labeling in Drosophila melanogaster09:59

In Vivo Application of TurboID-based Proximity Labeling in Drosophila melanogaster

Published on: June 13, 2025

1.4K

相关概念视频

Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes02:16

Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes

The present-day mitochondrial and chloroplast genomes have retained some of the characteristics of their ancestral prokaryotes and also have acquired new attributes during their evolution within eukaryotic cells. Like prokaryotic genomes, mitochondrial and chloroplast genomes neither bind with histone-like proteins nor show complex packaging into chromosome-like structures, as observed in eukaryotes. Unlike mitotic cell divisions observed in eukaryotic cells, mitochondria and chloroplasts...
16.3K
Anatomy of Chloroplasts01:07

Anatomy of Chloroplasts

Green algae and plants, including green stems and unripe fruit, harbor chloroplasts—the vital organelles where photosynthesis takes place. In plants, the highest density of chloroplasts is found in the mesophyll cells of leaves.
119.4K
Export of Mitochondrial and Chloroplast Genes02:19

Export of Mitochondrial and Chloroplast Genes

A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred...
4.2K
Protein Transport to the Inner Chloroplast Membrane01:18

Protein Transport to the Inner Chloroplast Membrane

Proteins targeted to the inner chloroplast membrane, or plastid proteins, are transported by two general pathways: the stop-transfer and the re-insertion or post-import pathways. Most plastid proteins carry N-terminal transit sequences and internal import sequences targeting it to the specific chloroplast subcompartment. Proteins targeted by the stop-transfer pathway have internal hydrophobic sequences that inhibit their translocation into the stroma. As a result, these precursors are arrested...
2.5K
Light Acquisition02:16

Light Acquisition

In order to produce glucose, plants need to capture sufficient light energy. Many modern plants have evolved leaves specialized for light acquisition. Leaves can be only millimeters in width or tens of meters wide, depending on the environment. Due to competition for sunlight, evolution has driven the evolution of increasingly larger leaves and taller plants, to avoid shading by their neighbors with contaminant elaboration of root architecture and mechanisms to transport water and nutrients.
9.6K
Protein Transport to the Outer Chloroplast Membrane01:11

Protein Transport to the Outer Chloroplast Membrane

Chloroplast outer membrane proteins encoded by the nucleus are synthesized in the cytosol. Soon after synthesis, they bind cytosolic factors such as 14-3-3 protein and the Hsp70 chaperones that keep these precursors in an unfolded state until their translocation.
Two models describe the mechanism of precursor recognition and entry across the outer membrane through the TOC complex. Model 1 suggests the newly synthesized precursor binds to the TOC receptor 159 and forms a complex.
2.4K