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Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein.
Transduction01:16

Transduction

Among the three main modes of HGT—transformation, conjugation, and transduction—transduction is unique in that it is mediated by bacteriophages, or bacterial viruses.Transduction occurs in two ways. Generalized transduction occurs during the lytic cycle of a bacteriophage infection. In this process, bacteriophages infect bacterial cells, replicate within them, and ultimately cause cell lysis, releasing newly assembled virions. Occasionally, random fragments of the bacterial genome are...
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,...
Protein Modifications in the RER01:26

Protein Modifications in the RER

Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal sequences.
Leaky Scanning02:28

Leaky Scanning

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 stands for...

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Updated: Jun 6, 2026

Utilizing a Comprehensive Immunoprecipitation Enrichment System to Identify an Endogenous Post-translational Modification Profile for Target Proteins
08:12

Utilizing a Comprehensive Immunoprecipitation Enrichment System to Identify an Endogenous Post-translational Modification Profile for Target Proteins

Published on: January 8, 2018

Las modificaciones postraslacionales mediadas por patógenos: un campo reemergente.

David Ribet1, Pascale Cossart

  • 1Institut Pasteur, Département de Biologie Cellulaire et Infection, Paris, France.

Cell
|November 30, 2010
PubMed
Resumen
Este resumen es generado por máquina.

Los patógenos usan modificaciones posttraducionales para manipular las vías de señalización de las células huésped, como NF-kB y MAP quinasa, ayudando a su supervivencia y propagación. Comprender estos mecanismos es crucial para el desarrollo de nuevas terapias anti-infecciosas.

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Isolation of Intermediate Filament Proteins from Multiple Mouse Tissues to Study Aging-associated Post-translational Modifications
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Isolation of Intermediate Filament Proteins from Multiple Mouse Tissues to Study Aging-associated Post-translational Modifications

Published on: May 18, 2017

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Utilizing a Comprehensive Immunoprecipitation Enrichment System to Identify an Endogenous Post-translational Modification Profile for Target Proteins
08:12

Utilizing a Comprehensive Immunoprecipitation Enrichment System to Identify an Endogenous Post-translational Modification Profile for Target Proteins

Published on: January 8, 2018

Isolation of Intermediate Filament Proteins from Multiple Mouse Tissues to Study Aging-associated Post-translational Modifications
09:29

Isolation of Intermediate Filament Proteins from Multiple Mouse Tissues to Study Aging-associated Post-translational Modifications

Published on: May 18, 2017

Área de la Ciencia:

  • Microbiología Microbiología.
  • Inmunología Inmunología.
  • Biología Molecular Biología Molecular

Sus antecedentes:

  • Los patógenos emplean estrategias sofisticadas para superar las defensas del huésped.
  • Las modificaciones postraslacionales (PTM) son eventos moleculares críticos en los procesos celulares.

Objetivo del estudio:

  • Para resaltar el papel de los PTM derivados de patógenos en la manipulación de la señalización celular del huésped.
  • Para subrayar la importancia de las PTM en la infección, la replicación y la evasión inmune.

Principales métodos:

  • Revisión de estudios recientes sobre el patógeno PTM y las interacciones de la vía huésped.
  • Análisis de cómo los PTM se dirigen a las cascadas de señalización de huéspedes clave.

Principales resultados:

  • Los patógenos utilizan PTM para modular eficazmente los factores del huésped esenciales para la infección.
  • Se demuestra la orientación específica de las vías de la quinasa NF-kB y MAP por parte de los PTM patógenos.
  • Se ha demostrado que las PTM son vitales para la replicación, la propagación y la evasión inmunológica del patógeno.

Conclusiones:

  • Los PTM mediados por patógenos representan un mecanismo significativo para subvertir la inmunidad del huésped.
  • Estos hallazgos ofrecen nuevos conocimientos sobre las interacciones entre patógeno y huésped.
  • Una mayor investigación sobre las PTM puede conducir al desarrollo de estrategias terapéuticas innovadoras contra las enfermedades infecciosas.