Literature DB >> 6933555

Ligand-linked phase changes in a biological system: applications to sickle cell hemoglobin.

J Wyman, S J Gill.   

Abstract

Polyphasic linkage is a close analog of the allosteric and polysteric linkages shown by many biological macromolecules. Like them, it gives rise to both homotropic and heterotropic effects. It is governed by a group of linkage potentials applicable to each separate phase and also, subject to certain conditions, by a group of lower order applicable to the whole system, globally. A good example of polyphasic linkage is provided by sickle cell hemoglobin which, under suitable conditions and subject to control by oxygen, precipitates out of solution to form what appear to be microtubules. This is but one instance of the way in which macromolecular assembly and the formation of subcellular structures generally can be regulated by various small molecules acting as ligands.

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Year:  1980        PMID: 6933555      PMCID: PMC350033          DOI: 10.1073/pnas.77.9.5239

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  12 in total

1.  Supersaturation in sickle cell hemoglobin solutions.

Authors:  J Hofrichter; P D Ross; W A Eaton
Journal:  Proc Natl Acad Sci U S A       Date:  1976-09       Impact factor: 11.205

Review 2.  The mechanism and prevention of sickling.

Authors:  A May; E R Huehns
Journal:  Br Med Bull       Date:  1976-09       Impact factor: 4.291

3.  A group of thermodynamic potentials applicable to ligand binding by a polyfunctional macromolecule.

Authors:  J Wyman
Journal:  Proc Natl Acad Sci U S A       Date:  1975-04       Impact factor: 11.205

4.  Polysteric linkage.

Authors:  A Colosimo; M Brunori; J Wyman
Journal:  J Mol Biol       Date:  1976-01-05       Impact factor: 5.469

5.  Relations between oxygen saturation and aggregation of sickle-cell hemoglobin.

Authors:  A P Minton
Journal:  J Mol Biol       Date:  1976-02-05       Impact factor: 5.469

6.  Analysis of non-ideal behavior in concentrated hemoglobin solutions.

Authors:  P D Ross; A P Minton
Journal:  J Mol Biol       Date:  1977-05-25       Impact factor: 5.469

7.  Oxygen binding to sickle cell hemoglobin.

Authors:  S J Gill; R C Benedict; L Fall; R Spokane; J Wyman
Journal:  J Mol Biol       Date:  1979-05-15       Impact factor: 5.469

8.  Concerted changes in an allosteric macromolecule.

Authors:  A Colosimo; M Brunori; J Wyman
Journal:  Biophys Chem       Date:  1974-12       Impact factor: 2.352

9.  Ligand-linked phase equilibria of sickle cell hemoglobin.

Authors:  S J Gill; R Spokane; R C Benedict; L Fall; J Wymann
Journal:  J Mol Biol       Date:  1980-06-25       Impact factor: 5.469

10.  Aggregation effects on oxygen binding of sickle cell hemoglobin.

Authors:  S J Gill; R Skold; L Fall; T Shaeffer; P Spokane; J Wyman
Journal:  Science       Date:  1978-07-28       Impact factor: 47.728

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  18 in total

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Journal:  J Biol Chem       Date:  2018-01-22       Impact factor: 5.157

5.  ALS-Linked Mutations Affect UBQLN2 Oligomerization and Phase Separation in a Position- and Amino Acid-Dependent Manner.

Authors:  Thuy P Dao; Brian Martyniak; Ashley J Canning; Yongna Lei; Erica G Colicino; Michael S Cosgrove; Heidi Hehnly; Carlos A Castañeda
Journal:  Structure       Date:  2019-04-11       Impact factor: 5.006

6.  Collective Learnings of Studies of Stress Granule Assembly and Composition.

Authors:  Hadjara Sidibé; Christine Vande Velde
Journal:  Methods Mol Biol       Date:  2022

Review 7.  Learning the chemical grammar of biomolecular condensates.

Authors:  Henry R Kilgore; Richard A Young
Journal:  Nat Chem Biol       Date:  2022-06-27       Impact factor: 16.174

8.  Ubiquitin Modulates Liquid-Liquid Phase Separation of UBQLN2 via Disruption of Multivalent Interactions.

Authors:  Thuy P Dao; Regina-Maria Kolaitis; Hong Joo Kim; Kevin O'Donovan; Brian Martyniak; Erica Colicino; Heidi Hehnly; J Paul Taylor; Carlos A Castañeda
Journal:  Mol Cell       Date:  2018-03-08       Impact factor: 17.970

9.  DMA-tudor interaction modules control the specificity of in vivo condensates.

Authors:  Edward M Courchaine; Andrew E S Barentine; Korinna Straube; Dong-Ryoung Lee; Joerg Bewersdorf; Karla M Neugebauer
Journal:  Cell       Date:  2021-06-10       Impact factor: 66.850

Review 10.  Polyphasic linkage and the impact of ligand binding on the regulation of biomolecular condensates.

Authors:  Kiersten M Ruff; Furqan Dar; Rohit V Pappu
Journal:  Biophys Rev       Date:  2021-06-15
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