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October 1, 1998Physiological Reviews581 citations

Phospholamban: Protein Structure, Mechanism of Action, and Role in Cardiac Function

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HSHeather K.B. SimmermanAmgen (United States)LJLarry R. JonesUniversity of Vermont

Key Points

  • The aim is to discuss the structure, mechanism, and physiological significance of phospholamban in cardiac function.
  • Review of historical studies on phospholamban and its gene structure, expression, and regulation.
  • Analysis of in vitro and in vivo studies on PLB protein structure and activity.
  • Use of advanced experimental techniques to explore PLB's interaction with Ca2+-ATPase.
  • Establishment of structural insights into phospholamban's role in regulating Ca2+-ATPase activity.
  • Identification of phospholamban's interaction dynamics contributing to cardiac functionality.
  • Emphasis on the potential therapeutic implications of phospholamban in heart failure.

Abstract

A comprehensive discussion is presented of advances in understanding the structure and function of phospholamban (PLB), the principal regulator of the Ca2+-ATPase of cardiac sarcoplasmic reticulum. Extensive historical studies are reviewed to provide perspective on recent developments. Phospholamban gene structure, expression, and regulation are presented in addition to in vitro and in vivo studies of PLB protein structure and activity. Applications of breakthrough experimental technologies in identifying PLB structure-function relationships and in defining its interaction with the Ca2+-ATPase are also highlighted. The current leading viewpoint of PLB's mechanism of action emerges from a critical examination of alternative hypotheses and the most recent experimental evidence. The potential physiological relevance of PLB function in human heart failure is also covered. The interest in PLB across diverse biochemical disciplines portends its continued intense scrutiny and its potential exploitation as a therapeutic target.

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Cite This Study

Simmerman et al. (1998) studied this question.

synapsesocial.com/papers/6a0795c5396fe5b3a88b3792https://doi.org/10.1152/physrev.1998.78.4.921
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Adenosine 3', 5'-Monophosphate-Dependent Membrane Phosphorylation1974 · 155 citations
  2. 2The calcium pump of cardiac sarcoplasmic reticulum. Functional alterations at different levels of thyroid state in rabbits1973 · 145 citations
  3. 3STRUCTURAL PERSPECTIVES OF PHOSPHOLAMBAN, A HELICAL TRANSMEMBRANE PENTAMER1997 · 70 citations
  4. 4Phospholamban of cardiac sarcoplasmic reticulum consists of two functionally distinct proteolipids1983 · 16 citations
  5. 5Phosphorylation of phospholamban in intact myocardium. Role of Ca2+-calmodulin-dependent mechanisms.1985 · 126 citations