4.5 Article

Modeling general proteostasis: proteome balance in health and disease

Journal

CURRENT OPINION IN CELL BIOLOGY
Volume 23, Issue 2, Pages 126-134

Publisher

CURRENT BIOLOGY LTD
DOI: 10.1016/j.ceb.2010.11.001

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Funding

  1. NHLBI NIH HHS [R01 HL079442-06, R01 HL095524, R01 HL079442, R01 HL095524-02] Funding Source: Medline
  2. NIA NIH HHS [R21 AG032552-02, RC2 AG036634-02, RC2 AG036634, R21 AG032552] Funding Source: Medline
  3. NIGMS NIH HHS [R01 GM042336, R01 GM042336-21, R01 GM033301, R01 GM033301-28] Funding Source: Medline
  4. NINDS NIH HHS [R21 NS067643, R21 NS067643-01] Funding Source: Medline

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Protein function is generated and maintained by the proteostasis network (PN) (Balch et al. (2008) Science, 319:916). The PN is a modular, yet integrated system unique to each cell type that is sensitive to signaling pathways that direct development and aging, and respond to folding stress. Mismanagement of protein folding and function triggered by genetic, epigenetic and environmental causes poses a major challenge to human health and lifespan. Herein, we address the impact of proteostasis defined by the FoldFx model on our understanding of protein folding and function in biology. FoldFx describes how general proteostasis control (GPC) enables the polypeptide chain sequence to achieve functional balance in the context of the cellular proteome. By linking together the chemical and energetic properties of the protein fold with the composition of the PN we discuss the principle of the proteostasis boundary (PB) as a key component of GPC. The curved surface of the PB observed in 3-dimensional space suggests that the polypeptide chain sequence and the PN operate as an evolutionarily conserved functional unit to generate and sustain protein dynamics required for biology. Modeling general proteostasis provides a rational basis for tackling some of the most challenging diseases facing mankind in the 21st century.

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