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Protein translocation in apoptosis

A G Porter1

  • 1Institute of Molecular and Cell Biology, An institute affiliated to The National University of Singapore, 30 Medical Drive, Singapore 117609, Republic of Singapore. mcbagp@imcb.nus.edu.sg

Trends in Cell Biology
|September 11, 1999
PubMed

Insights

Programmed cell death, or apoptosis, involves signals triggering protein movement to various cell parts. This review explores how protein translocation regulates and executes apoptosis.

Area of Science:

  • Cell Biology
  • Molecular Biology
  • Biochemistry

Background:

  • Programmed cell death (apoptosis) is a fundamental biological process involving widespread cellular alterations.
  • Signaling pathways initiate apoptosis, affecting all cellular compartments.
  • Protein translocation is increasingly recognized for its critical role in apoptosis.

Purpose of the Study:

  • To review the mechanisms, locations, and reasons for protein translocation during apoptosis.
  • To highlight the significance of protein translocation in apoptosis execution and regulation.
  • To provide a comprehensive overview of protein movement in programmed cell death.

Main Methods:

  • Literature review of scientific publications on apoptosis and protein translocation.
  • Analysis of diverse protein translocation mechanisms.
  • Synthesis of information on protein movement to and from key cellular organelles.

Main Results:

  • Protein translocation occurs to and from the plasma membrane, mitochondria, and nucleus during apoptosis.
  • Diverse mechanisms mediate these protein movements.
  • These translocations are integral to the induction, amplification, and regulation of apoptosis.

Conclusions:

  • Protein translocation is a key regulatory and execution step in apoptosis.
  • Understanding these events is crucial for comprehending programmed cell death.
  • Further research into specific translocation pathways can reveal therapeutic targets.

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