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Extraction: Effects of pH00:53

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Consider a neutral form of an amine, B, with a partition coefficient, K, in a liquid mixture containing organic and aqueous phases. The pH of the aqueous phase affects the charge on acidic and basic solutes, and the charged form is usually more soluble in the aqueous phase. Suppose the conjugate acid form of the amine is soluble only in the aqueous phase while the base form is soluble in both phases. Then the distribution coefficient, D, can be given as the ratio of amine concentration in the...
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Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
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The distribution law or Nernst's distribution law is the law that governs the distribution of a solute between two immiscible solvents. This law, also known as the partition law, states that if a solute is added to the mixture of two immiscible solvents at a constant temperature, the solute is distributed between the two solvents in such a way that the ratio of solute concentrations in the solvents remains constant at equilibrium.
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Antiepileptic drugs, such as levetiracetam (Keppra) and brivaracetam (Briviact), have emerged as crucial tools in managing epilepsy. These medications exert their therapeutic effects by targeting the synaptic vesicle protein SV2A, a transmembrane glycoprotein primarily found in the brain.
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Many cellular signals are hydrophilic and therefore cannot pass through the plasma membrane. However, small or hydrophobic signaling molecules can cross the hydrophobic core of the plasma membrane and bind to internal, or intracellular, receptors that reside within the cell. Many mammalian steroid hormones use this mechanism of cell signaling, as does nitric oxide (NO) gas.
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Cooperative allosteric transitions can occur in multimeric proteins, where each subunit of the protein has its own ligand-binding site. When a ligand binds to any of these subunits, it triggers a conformational change that affects the binding sites in the other subunits; this can change the affinity of the other sites for their respective ligands. The ability of the protein to change the shape of its binding site is attributed to the presence of a mix of flexible and stable segments in the...
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Recursive module extraction using Louvain and PageRank.

Dimitri Perrin1, Guido Zuccon1

  • 1School of Electrical Engineering and Computer Science, Queensland University of Technology, Brisbane, QLD, 4001, Australia.

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|October 2, 2018
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Summary
This summary is machine-generated.

This study introduces a novel recursive method combining the Louvain algorithm and PageRank to identify functional modules in biological networks. The approach effectively detects significant disease-related modules, though results show variability.

Keywords:
Community detectionDREAM challengeModule identificationNetwork biology

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Area of Science:

  • Systems Biology
  • Network Science
  • Computational Biology

Background:

  • Biological networks exhibit modularity, with clusters often linked to specific biological functions or diseases.
  • Identifying these functional modules is crucial for understanding biological systems but remains a complex challenge.

Purpose of the Study:

  • To develop and evaluate a novel recursive method for identifying significant modules in biological networks.
  • To leverage community detection and network weighting algorithms for enhanced module identification.

Main Methods:

  • A recursive approach integrating the Louvain algorithm for community detection and the PageRank algorithm for node weighting.
  • PageRank initializes node weights, followed by Louvain algorithm application with the Newman-Girvan modularity criterion.
  • Modules exceeding a threshold size (k) are recursively processed until no module surpasses k nodes.

Main Results:

  • The proposed method demonstrates effectiveness in identifying a substantial number of significant biological modules across diverse network types.
  • Evaluation on six biological networks from the Disease Module Identification DREAM Challenge confirmed the method's utility.
  • A notable finding includes substantial variability in module identification across different method restarts.

Conclusions:

  • The recursive PageRank-Louvain method offers a promising strategy for biological module discovery.
  • The approach successfully identifies functional and disease-associated clusters within complex biological networks.
  • Further refinement may be needed to address the observed variability in results.