Jove
Visualize
お問い合わせ
JoVE
x logofacebook logolinkedin logoyoutube logo
JoVEについて
概要リーダーシップブログJoVEヘルプセンター
著者向け
出版プロセス編集委員会範囲と方針査読よくある質問投稿
図書館員向け
推薦の声購読アクセスリソース図書館諮問委員会よくある質問
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experimentsアーカイブ
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教員リソースセンター教員サイト
利用規約
プライバシーポリシー
ポリシー

関連する概念動画

Assembly of Signaling Complexes01:30

Assembly of Signaling Complexes

4.7K
Multiprotein signaling complexes are formed in a dynamic process involving protein-protein interactions at the cytoplasmic domain of transmembrane receptors or enzymatic and non-enzymatic proteins associated with the receptor. These complexes ensure the activation and propagation of intracellular signals that regulate cell functions.
Interaction domains in cell signaling
Interaction domains recognize exposed features of their binding partners containing post-translationally modified sequences,...
4.7K
Calmodulin-dependent Signaling01:16

Calmodulin-dependent Signaling

4.9K
Calmodulin (CaM) is a calcium-binding protein in eukaryotes that controls various calcium-regulated cellular processes. It has four calcium-binding sites that bind calcium to form the calcium-calmodulin ( Ca2+-CaM) complex. GPCR stimulation increases the calcium levels in the cells that bind to CaM and induces a conformational change.
The Ca2+-CaM complex does not have enzymatic activity by itself. Instead, the complex binds downstream target proteins, including membrane proteins or enzymes,...
4.9K
Signal Transduction: Overview01:26

Signal Transduction: Overview

8.5K
Cells respond to many types of information, often through receptor proteins positioned on the membrane. They respond to chemical signals, such as hormones, neurotransmitters, and other signaling molecules, initiating a series of molecular reactions to produce an appropriate response. This is called signal transduction. Cells also coordinate different responses elicited by the same signaling molecule via mediators, allowing molecular cross-talk.
Typically, signal transduction involves three...
8.5K
Amplifying Signals via Second Messengers01:15

Amplifying Signals via Second Messengers

6.1K
Many receptor binding ligands are hydrophilic; they do not cross the cell membrane but bind to cell-surface receptors. Thus, their message must be relayed by second messengers present in the cell cytoplasm. There are several second messenger pathways, each with its own way of relaying information. For example, the G protein-coupled receptors can activate both phosphoinositol and cyclic AMP (cAMP) second messenger pathways. The phosphoinositol pathway is active when the receptor induces...
6.1K
Amplifying Signals via Enzymatic Cascade01:22

Amplifying Signals via Enzymatic Cascade

15.1K
When a ligand binds to a cell-surface receptor, the receptor's intracellular domain changes shape, which may either activate its enzyme function or allow its binding to other molecules. The initial signal is amplified by most signal transduction pathways. This means that a single ligand molecule can activate multiple molecules of a downstream target. Proteins that relay a signal are most commonly phosphorylated at one or more sites, activating or inactivating the protein. Kinases catalyze...
15.1K
Cell-surface Signaling01:21

Cell-surface Signaling

92.4K
Hormones—or any molecule that binds to a receptor, known as a ligand—that are lipid-insoluble (water-soluble) are not able to diffuse across the cell membrane. In order to be able to affect a cell without entering it, these hormones bind to receptors on the cell membrane. When a first messenger, a hormone, binds to a receptor, a signal cascade is set off, causing second messengers, proteins inside the cell, to become activated, resulting in downstream effects.
92.4K

こちらも読む

関連記事

共著者、ジャーナル、引用グラフによってこの研究に関連する記事。

並び替え
Same author

Cytocompatible Biocatalyzed Surface-Initiated PhotoATRP Mediated by Red Light Irradiation in Open Air.

JACS Au·2026
Same author

Material-dependent trueness of intraoral scanners: A comparative analysis of three scanning technologies for different crowns - An in vitro study.

Journal of Indian Prosthodontic Society·2026
Same author

Protein migration <i>via</i> dissolution of ATP-stabilized condensate in a gradient of AMP.

Chemical communications (Cambridge, England)·2026
Same author

Stress evaluation of different cad-on material combinations in crown design over conventional hand-layered zirconia - an in vitro 3d finite element analysis.

Revista cientifica odontologica (Universidad Cientifica del Sur)·2026
Same author

Near-Quantitative Formation of Imines in Water with Allosteric Control.

Journal of the American Chemical Society·2026
Same author

Comparative Assessment of Microleakage in Nanoformulated and Conventional Glass Ionomer Cement under Simulated Aging: A Stereomicroscopic Study.

International journal of clinical pediatric dentistry·2026

関連する実験動画

Updated: Apr 26, 2026

Measuring Transcellular Interactions through Protein Aggregation in a Heterologous Cell System
04:47

Measuring Transcellular Interactions through Protein Aggregation in a Heterologous Cell System

Published on: May 22, 2020

2.7K

多価相互作用は,自己組み立てのHg2+センサーの信号伝導を調節する.

Subhabrata Maiti1, Cristian Pezzato, Sergio Garcia Martin

  • 1Department of Chemical Sciences, University of Padova , Via Marzolo 1, 35131 Padova, Italy.

Journal of the American Chemical Society
|July 24, 2014
PubMed
まとめ

この研究は,低ナノモラーレベルでの水銀イオン (Hg2+) を検出するための新しい自己組み立てセンサーを導入しています. システムは,敏感で選択的な信号伝導のための多価相互作用を利用し,光反応の"オン"を可能にします.

科学分野:

  • 化学センサー 化学センサー
  • ナノテクノロジー ナノテクノロジー
  • バイオ分子相互作用

背景:

  • 水銀イオン (Hg2+) は,環境と健康に重大なリスクをもたらす.
  • Hg2+の敏感で選択的な検出方法の開発は極めて重要です.
  • 既存の方法は,しばしば効率が欠けているか,複雑な手順を必要とする.

研究 の 目的:

  • 低ナノモラーHg2+検出のための自己組み立てセンサーシステムを開発する.
  • 信号伝導のための多価相互作用を活用する.
  • 調節可能な出力信号と選択的複合体の形成を実証する.

主な方法:

  • マルチバレント相互作用に基づくセンサーシステムの設計.
  • 分析剤の結合時に二酸化する低親和性リガンドを使用する.
  • モノレイヤーで保護された金ナノ粒子 (AuNPs) を多価表面で使用します.
  • 信号読み出しの光消し/消し止めメカニズムを実装する.

主要な成果:

  • このシステムは,低ナノモラー濃度でHg2+を成功裏に検出します.
  • アナリート誘発的二分化により,AuNPs.を持つ高親和複合体の形成が生じます.

さらに関連する動画

Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes
07:22

Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes

Published on: January 12, 2024

4.5K
Imaging G-protein Coupled Receptor GPCR-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum
09:40

Imaging G-protein Coupled Receptor GPCR-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum

Published on: September 20, 2011

17.0K

関連する実験動画

Last Updated: Apr 26, 2026

Measuring Transcellular Interactions through Protein Aggregation in a Heterologous Cell System
04:47

Measuring Transcellular Interactions through Protein Aggregation in a Heterologous Cell System

Published on: May 22, 2020

2.7K
Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes
07:22

Author Spotlight: Evaluating Biophysical Assays for Characterizing PROTACS Ternary Complexes

Published on: January 12, 2024

4.5K
Imaging G-protein Coupled Receptor GPCR-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum
09:40

Imaging G-protein Coupled Receptor GPCR-mediated Signaling Events that Control Chemotaxis of Dictyostelium Discoideum

Published on: September 20, 2011

17.0K
  • 消し去られたレポーターの移動時に"オン"の光信号が観測される.
  • 信号の強さは,多価相互作用を調節することによって調節できます.
  • 多価相互作用は,高親和複合体の自己選択を誘導する.
  • 結論:

    • Hg2+を検出するための新しい自己組み立てセンサーが紹介されています.
    • このシステムは,敏感で選択的な信号伝達のために,多変量相互作用を活用しています.
    • この発見は,高度な化学センサーを開発するための新しいプラットフォームを提供します.