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Related Concept Videos

Molecular Models02:00

Molecular Models

Physical models representing molecular architectures of chemical compounds play essential roles in understanding chemistry. The use of molecular models makes it easier to visualize the structures and shapes of atoms and molecules.
Super-resolution Fluorescence Microscopy01:37

Super-resolution Fluorescence Microscopy

Super-resolution fluorescence microscopy (SRFM) provides a better resolution than conventional fluorescence microscopy by reducing the point spread function (PSF). PSF is the light intensity distribution from a point that causes it to appear blurred. Due to PSF, each fluorescing point appears bigger than its actual size, and it is the PSF interference of nearby fluorophores that causes the blurred image. Various approaches to achieving higher resolution through SRFM have recently been developed.
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
Crystal Growth: Principles of Crystallization01:25

Crystal Growth: Principles of Crystallization

Crystallization is a phase transformation process in which crystals are precipitated from a supersaturated solution or formed from other sources. During crystallization, atoms or molecules arrange themselves into a well-defined, rigid crystal lattice to minimize energy.
Initiating crystallization involves manipulating the concentration of the solute and the temperature of the solution. Since crystal growth occurs when the ratio of concentration and solubility of the solute in the solvent – the...
Crystal Density01:19

Crystal Density

The crystal lattice structure of a material allows us to determine how many molecules exist in its unit cell. With this information, alongside the unit-cell parameters - three distance parameters (a, b, c) and three angular parameters (α, β, γ).Density (ρ) = (Z × M) / (a × b × c × NA)where:Z is the number of formula units per unit cellM is the molar mass of the substancea, b, and c are the edge lengths of the unit cellNA is Avogadro’s numberFor a simple cubic lattice, atoms are located only at...
X-ray Crystallography02:18

X-ray Crystallography

The size of the unit cell and the arrangement of atoms in a crystal may be determined from measurements of the diffraction of X-rays by the crystal, termed X-ray crystallography.
Diffraction
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Corrigendum to "Association between interleukin-6, suPAR, and hsCRP with subclinical left ventricular dysfunction in type 1 diabetes: The Thousand & 1 study" [Diabetes Res. Clin. Pract. 222 (2025) 112071].

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Related Experiment Video

Updated: Jun 18, 2026

On-Chip Crystallization and Large-Scale Serial Diffraction at Room Temperature
07:42

On-Chip Crystallization and Large-Scale Serial Diffraction at Room Temperature

Published on: March 11, 2022

suPAR: the molecular crystal ball.

Maria Thunø1, Betina Macho, Jesper Eugen-Olsen

  • 1Virogates A/S, Blokken 45, DK-3460 Birkerød, Denmark.

Disease Markers
|November 7, 2009
PubMed
Summary

Soluble urokinase Plasminogen Activator Receptor (suPAR) fragments play distinct roles in inflammation. Understanding these suPAR forms and their mechanisms could lead to new treatments for infectious and pathological conditions.

Area of Science:

  • Biochemistry
  • Immunology
  • Molecular Biology

Background:

  • Soluble urokinase Plasminogen Activator Receptor (suPAR) levels indicate inflammation, often elevated in infections and cancer.
  • suPAR exists in three distinct forms: suPAR(I-III), suPAR(II-III), and suPAR(I), each with unique properties.

Purpose of the Study:

  • To review the different suPAR fragments and their roles in inflammation and disease.
  • To explore the molecular mechanisms of suPAR fragments in inflammatory processes.

Main Methods:

  • Literature review focusing on suPAR fragments.
  • Analysis of molecular mechanisms linking suPAR fragments to inflammation.

Main Results:

  • Full-length suPAR may act as a uPA-scavenger, regulating uPAR/uPA.

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  • Cleaved suPAR(II-III) functions as a chemotactic agent, promoting immune response via its SRSRY sequence.
  • Conclusions:

    • The distinct functions of suPAR fragments in inflammation are crucial.
    • Further understanding of suPAR fragment mechanisms may offer novel therapeutic strategies for inflammatory and pathological conditions.