Cited by 28Protein Kinase Regulation and GTPase SignalingLipid Membrane Structure and BehaviorCellular transport and secretion

Does PtdIns(4,5)P 2 concentrate so it can multi-task?

Hammond, Gerald R.V.·2016·Biochemical Society Transactions

Abstract

Ptdns(4,5)P2 is a minor structural lipid of the plasma membrane (PM), but a master regulator of PM function. Serving either as a substrate for the generation of second messengers, or more commonly as a ligand triggering protein recruitment or activation, it regulates most aspects of PM function. Understanding how this relatively simple biological macromolecule can regulate such a vast array of different functions in parallel, is the key to understanding the biology of the PM as a whole, in both health and disease. In this review, potential mechanisms are discussed that might explain how a lipid can separately regulate so many protein complexes. The focus is on the spatial distribution of the lipid molecules, their metabolism and their interactions. Open questions that still need to be resolved are highlighted, as are potential experimental approaches that might shed light on the mechanisms at play. Moreover, the broader question is raised as to whether PtdIns(4,5)P2 should be thought of as a bona fide signalling molecule or more of a simple lipid cofactor or perhaps both, depending on the context of the particular function in question.

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Crossref · 10.1042/bst20150211

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2 of 2 references verified0 citation errors · 0 not checkable

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  • There is strong evidence for PI(4,5)P2 segregation, but many caveats remain due to technical limitations.

    “Although there is strong evidence to support segregation of PI(4,5)P2, as discussed above, there remains many caveats due to technical limitations [132,133].”
  • Local enrichment of PI(4,5)P2 can occur by preferential trapping in lipid rafts, binding proteins such as MARCKS, syntaxin-1 and K-Ras, or localised recruitment of PIP5K.

    “Local enrichment of PI(4,5)P2 can occur by multiple mechanisms [131,132]. There can be preferential trapping of PI(4,5)P2 in lipid rafts, binding proteins such as MARCKS (myristoylated alanine-rich C-kinase substrate), syntaxin-1 and K-Ras that sequester PI(4,5)P2, or localised recruitment of PIP5K to generate PI(4,5)P2.”

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Authors
Hammond, G. R. V.
Affiliations
University of Pittsburgh (US)
Corresponding author
Hammond, Gerald R.V.
Venue
Biochemical Society Transactions
Published
2016-02-09
Volume
44
Issue
1
Pages
228-233
ISSN
  • 0300-5127 (ISSN-L)
  • 1470-8752
OpenAlex
W2310769659
Cited by
28
References
2
Citations by year
2026: 2 · 2025: 1 · 2024: 3 · 2023: 1 · 2022: 4 · 2021: 4 · 2020: 5 · 2019: 1 · 2018: 3 · 2017: 3 · 2016: 1
FWCI
0.24
Type
journal article
Language
en
Open access
closed
Locations
  • Biochemical Society Transactions (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Kinase Regulation and GTPase Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Lipid Membrane Structure and Behavior
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Cellular transport and secretion
Keywords
phosphatidylinositol 4,5-bisphosphate, plasma membrane, lipid signaling, lipid spatial distribution, lipid metabolism, protein-lipid interactions, second messengers, protein recruitment, lipid cofactors
MeSH terms
Animals, Cell Membrane, Humans, Models, Biological, Phosphatidylinositol 4,5-Diphosphate

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