Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Amplifying Signals via Enzymatic Cascade01:22

Amplifying Signals via Enzymatic Cascade

15.3K
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...
15.3K
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
IP3/DAG Signaling Pathway01:11

IP3/DAG Signaling Pathway

12.5K
Membrane lipids such as phosphatidylinositol (PI) are precursors for several membrane-bound and soluble second messengers. Specific kinases phosphorylate PI and produce phosphorylated inositol phospholipids. One such inositol phospholipids are the  phosphatidylinositol-4,5 bisphosphate [PI(4,5)P2], present in the inner half of the lipid bilayer. Upon ligand binding, GPCR stimulates Gq proteins to turn on phospholipase Cꞵ. Activated phospholipase Cꞵ cleaves PI(4,5)P2 and...
12.5K
Transducer Mechanism: Enzyme-Linked Receptors01:27

Transducer Mechanism: Enzyme-Linked Receptors

4.4K
Enzyme-linked receptors are cell-surface receptors acting as an enzyme or associating with an enzyme intracellularly. They make excellent drug targets. Drugs can bind to the extracellular ligand-binding domain or directly affect their enzymatic domain and alter their activity.
Major types that are helpful drug targets include:
4.4K
Intracellular Signaling Cascades01:24

Intracellular Signaling Cascades

44.8K
Once a ligand binds to a receptor, the signal is transmitted through the membrane and into the cytoplasm. The continuation of a signal in this manner is called signal transduction. Signal transduction only occurs with cell-surface receptors, which cannot interact with most components of the cell, such as DNA. Only internal receptors can interact directly with DNA in the nucleus to initiate protein synthesis. When a ligand binds to its receptor, conformational changes occur that affect the...
44.8K
Interactions Between Signaling Pathways01:19

Interactions Between Signaling Pathways

4.7K
Signaling cascades usually lack linearity. Multiple pathways interact and regulate one another, allowing cells to integrate and respond to diverse environmental stimuli.
Convergence and divergence, and cross-talk between signaling pathways
Two distinct signaling pathways can converge on a single functional unit, which may either be a single protein or a complex of proteins. The response is either functionally distinct or synergistic between the two pathways but different from the response...
4.7K

También podría leer

Artículos Relacionados

Artículos vinculados a este trabajo por autores compartidos, revista y gráfico de citas.

Ordenar por
Same author

Correction to "Direct Intracellular Delivery of Benzene Diazonium Ions As Observed by Increased Tyrosine Phosphorylation".

Biochemistry·2022
Same author

Direct Intracellular Delivery of Benzene Diazonium Ions As Observed by Increased Tyrosine Phosphorylation.

Biochemistry·2022
Same author

A Self-Replicating Peptide under Ionic Control.

Angewandte Chemie (International ed. in English)·2018
Same author

Discovery of Potent and Selective A<sub>2A</sub> Antagonists with Efficacy in Animal Models of Parkinson's Disease and Depression.

ACS medicinal chemistry letters·2017
Same author

Design and synthesis of novel xanthine derivatives as potent and selective A<sub>2B</sub> adenosine receptor antagonists for the treatment of chronic inflammatory airway diseases.

European journal of medicinal chemistry·2017
Same author

Engineering Small Molecule Responsive Split Protein Kinases.

Methods in molecular biology (Clifton, N.J.)·2017
Same journal

Gas-Responsive Metal-Organic Frameworks for Adaptive Thermal Energy Storage with Tunable Charge-Discharge Temperatures.

Journal of the American Chemical Society·2026
Same journal

Engineering a Thiamine-Dependent Benzoylformate Decarboxylase for Stereodivergent Radical C(sp<sup>3</sup>)-C(sp<sup>3</sup>) Bond Formation.

Journal of the American Chemical Society·2026
Same journal

Accelerated Directional Proton-Coupled Electron Transfer Enabled by Intrinsic Dipole Field in Biomimetic α-Helical Structure.

Journal of the American Chemical Society·2026
Same journal

Alternating Current-Driven Hydrogen Isotope Labeling of Aliphatic Amines Using 1,3-Propanedithiol as an Efficient Hydrogen Atom Transfer Reagent.

Journal of the American Chemical Society·2026
Same journal

Two-Dimensional van der Waals Polar Metal MoOBr<sub>2</sub>.

Journal of the American Chemical Society·2026
Same journal

Negatively Curved Chiral Bilayer Nanographene.

Journal of the American Chemical Society·2026
Ver todos los artículos relacionados
JoVE
x logofacebook logolinkedin logoyoutube logo
ACERCA DE JoVE
Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
AUTORES
Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
BIBLIOTECARIOS
TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
INVESTIGACIÓN
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
EDUCACIÓN
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
Términos y Condiciones de Uso
Política de Privacidad
Políticas

Video Experimental Relacionado

Updated: May 3, 2026

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
11:23

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein

Published on: June 30, 2019

6.0K

Las quinasas escindidas por ligandos.

Karla Camacho-Soto1, Javier Castillo-Montoya, Blake Tye

  • 1Department of Chemistry and Biochemistry, University of Arizona , 1306 East University Boulevard, Tucson, Arizona 85721, United States.

Journal of the American Chemical Society
|February 19, 2014
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores diseñaron proteínas quinasas para ser controladas por entradas definidas por el usuario. Este método crea quinasas de proteína dividida por ligandos a partir de fragmentos inactivos, lo que permite nuevas aplicaciones en biología molecular.

Más Videos Relacionados

Use of Label-free Optical Biosensors to Detect Modulation of Potassium Channels by G-protein Coupled Receptors
10:59

Use of Label-free Optical Biosensors to Detect Modulation of Potassium Channels by G-protein Coupled Receptors

Published on: February 10, 2014

9.5K
Spatiotemporal Control of Protein Activity through Optogenetic Allosteric Regulation
08:00

Spatiotemporal Control of Protein Activity through Optogenetic Allosteric Regulation

Published on: October 4, 2024

1.2K

Videos de Experimentos Relacionados

Last Updated: May 3, 2026

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein
11:23

Characterization at the Molecular Level using Robust Biochemical Approaches of a New Kinase Protein

Published on: June 30, 2019

6.0K
Use of Label-free Optical Biosensors to Detect Modulation of Potassium Channels by G-protein Coupled Receptors
10:59

Use of Label-free Optical Biosensors to Detect Modulation of Potassium Channels by G-protein Coupled Receptors

Published on: February 10, 2014

9.5K
Spatiotemporal Control of Protein Activity through Optogenetic Allosteric Regulation
08:00

Spatiotemporal Control of Protein Activity through Optogenetic Allosteric Regulation

Published on: October 4, 2024

1.2K

Área de la Ciencia:

  • La bioquímica es la bioquímica.
  • Biología Molecular Biología Molecular
  • Ingeniería de proteínas Ingeniería de proteínas.

Sus antecedentes:

  • La actividad de la proteína quinasa está regulada por insumos fisicoquímicos naturales como la fosforilación y los iones metálicos.
  • El diseño de proteínas cinasas sintéticas con control definido por el usuario es un desafío significativo en la biotecnología.

Objetivo del estudio:

  • Desarrollar un método para la ingeniería de proteínas cinasas sensibles a las entradas definidas por el usuario.
  • Para crear nuevas quinasas de proteína dividida por ligandos con actividad catalítica retenida.

Principales métodos:

  • Se utilizó un enfoque de disimilaridad de secuencias para identificar sitios adecuados para la inserción de bucles de residuos de 25 en las proteínacinasas.
  • Los mutantes de inserción de bucle exitosos guiaron la disección de las quinasas en fragmentos inactivos.
  • El reensamblaje de los fragmentos se desencadenó por la unión de ligandos para crear kinasas activas de proteína dividida.

Principales resultados:

  • Identificó sitios específicos en las proteínacinasas que toleran las inserciones de bucle mientras mantienen la función catalítica.
  • Se ha demostrado la ingeniería exitosa de las quinasas de proteína dividida por ligando utilizando Lyn, Fak, Src y PKA.
  • Mostró la generalidad potencial del enfoque desarrollado a través de diferentes familias de quinasas.

Conclusiones:

  • El método basado en la disimilaridad de secuencias es eficaz para diseñar proteínas quinasas controlables.
  • Este enfoque permite la creación de kinasas de proteínas divididas catalíticamente activas que responden a ligandos específicos.
  • Los hallazgos sugieren una amplia aplicabilidad para la ingeniería de kinasas personalizadas.