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Protein Organization01:24

Protein Organization

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Proteins are polymers of amino acid residues. They are versatile and responsible for different cellular functions, including DNA replication, molecular transport, catalysis, and structural support. Proteins have a hierarchical structure comprising at least three levels of organization: primary, secondary, and tertiary structure. Some large proteins have a quaternary structure where individual protein subunits are linked together.
The primary structure of a protein is its amino acid sequence....
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Protein Folding01:22

Protein Folding

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Overview
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Protein Folding01:25

Protein Folding

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Proteins are chains of amino acids linked together by peptide bonds. Upon synthesis, a protein folds into a three-dimensional conformation, critical to its biological function. Interactions between its constituent amino acids guide protein folding, and hence the protein structure is primarily dependent on its amino acid sequence.
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
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Conserved Binding Sites01:49

Conserved Binding Sites

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Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally...
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Amino acids03:42

Amino acids

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Amino acids are the monomers that comprise proteins. Each amino acid has the same fundamental structure, which consists of a central carbon atom, or the alpha (α) carbon, bonded to an amino group (NH2), a carboxyl group (COOH), and to a hydrogen atom. Every amino acid also has another atom or group of atoms bonded to the central atom known as the R group. There are 20 common amino acids present in proteins, each with a different R group. Variation in the amino acid sequence is responsible for...
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Updated: Jan 8, 2026

Author Spotlight: In Silico Creation and Impact of Carbonylated Amino Acids on Protein Structure and Function
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Author Spotlight: In Silico Creation and Impact of Carbonylated Amino Acids on Protein Structure and Function

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Aminoácidos Atrapados Dentro de C₁₀₀: Un Estudio Computacional

Satnam Singh1, Surajit Kayal2, Brijesh Kumar Mishra2

  • 1Department of Physical Sciences, Sant Baba Bhag Singh University, Jalandhar, Punjab, 144030, India.

Chemphyschem : a European journal of chemical physics and physical chemistry
|December 21, 2025
PubMed
Resumen
Este resumen es generado por máquina.

El fullereno C100 encapsula eficazmente aminoácidos como glicina, alanina y serina, mostrando interacciones favorables y estabilizando sus estructuras. La encapsulación altera los modos vibracionales y reduce los momentos dipolares, impactando sus propiedades electrónicas.

Palabras clave:
aminoácidosconfinamientodipéptidosfullereno C100energía de interacción

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Área de la Ciencia:

  • Química Computacional
  • Ciencia de Materiales
  • Nanotecnología

Sus antecedentes:

  • Los fullerenos, en particular C100, se exploran por su potencial como nanocontenedores.
  • Los aminoácidos son moléculas biológicas fundamentales con propiedades diversas.
  • La comprensión de las interacciones huésped-huésped a nanoescala es crucial para el desarrollo de nuevos materiales.

Objetivo del estudio:

  • Investigar la viabilidad de usar el fullereno C100 como nanocontenedor para glicina, alanina y serina.
  • Analizar las energías de interacción y la estabilidad estructural de los aminoácidos encapsulados.
  • Examinar los efectos de la encapsulación en los modos vibracionales, momentos dipolares y desplazamientos químicos de RMN de los aminoácidos.

Principales métodos:

  • Teoría de Funcionales de la Densidad (DFT) con el funcional B3LYP-D3.
  • Teoría de perturbaciones de Møller-Plesset de segundo orden (MP2).
  • Método de cúmulos acoplados de orbitales naturales de pares locales basados en dominios (DLPNO-CCSD(T)) para cálculos de alta precisión.

Principales resultados:

  • Las energías de interacción calculadas indican interacciones huésped-huésped favorables entre C100 y los aminoácidos (-47.8 a -43.8 kcal/mol).
  • La encapsulación estabiliza los conformadores de los aminoácidos, tanto los que forman enlaces de hidrógeno como los que no.
  • El análisis vibracional revela movimiento restringido (desplazamiento al azul) pero fortalecimiento de los enlaces de hidrógeno (desplazamiento al rojo en el estiramiento OH).
  • Se observa una reducción significativa de los momentos dipolares y desplazamientos hacia campo bajo en los desplazamientos químicos de RMN de 1H tras la encapsulación.

Conclusiones:

  • El fullereno C100 es un nanocontenedor viable para aminoácidos pequeños.
  • La encapsulación modifica significativamente las propiedades electrónicas y vibracionales de la glicina, alanina y serina.
  • La jaula C100 apantalla eficazmente los momentos dipolares e influye en la dinámica molecular.