4.7 Article

Delivery of Inorganic Polyphosphate into Cells Using Amphipathic Oligocarbonate Transporters

Journal

ACS CENTRAL SCIENCE
Volume 4, Issue 10, Pages 1394-1402

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acscentsci.8b00470

Keywords

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Funding

  1. Department of Energy [DE-SC0018168]
  2. National Science Foundation [NSF CHE-1607092, HFSP RGP0025, NIH-CA031845]
  3. Stanford Center for Molecular Analysis and Design (CMAD)
  4. Child Health Research Institute
  5. SPARK program at Stanford University
  6. NIH S10 Shared Instrument Grant [S10RR027431-01]
  7. NATIONAL CANCER INSTITUTE [R37CA031845, R01CA031845] Funding Source: NIH RePORTER
  8. NATIONAL CENTER FOR RESEARCH RESOURCES [S10RR027431] Funding Source: NIH RePORTER

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Inorganic polyphosphate (polyP) is an often-overlooked biopolymer of phosphate residues present in living cells. PolyP is associated with many essential biological roles. Despite interest in polyP's function, most studies have been limited to extracellular or isolated protein experiments, as polyanionic polyP does not traverse the nonpolar membrane of cells. To address this problem, we developed a robust, readily employed method for polyP delivery using guanidinium-rich oligocarbonate transporters that electrostatically complex polyPs of multiple lengths, forming discrete nanoparticles that are resistant to phosphatase degradation and that readily enter multiple cell types. Fluorescently labeled polyPs have been monitored over time for subcellular localization and release from the transporter, with control over release rates achieved by modulating the transporter identity and the charge ratio of the electrostatic complexes. This general approach to polyP delivery enables the study of intracellular polyP signaling in a variety of applications.

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