4.4 Article

Synthesis and two-photon photolysis of 6-(ortho-nitroveratryl)-caged IP3 in living cells

Journal

CHEMBIOCHEM
Volume 7, Issue 1, Pages 174-180

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.200500345

Keywords

caged compounds; calcium; photolysis; signal transduction; two-photon uncaging

Funding

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM053395] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [GM53395] Funding Source: Medline

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The synthesis of a photolabile derivative of inositol-1,4,5-trisphosphate (IP3) is described. This new caged second messenger (6-ortho-nitroveratryl)-IP3 (6-NV-IP3) has an extinction coefficient of 5000M(-1)cm(-1) at 350 rim, and a quantum yield of photolysis of 6-NV-IP3 is photolyzed with UV light about three 0.12. Therefore, 6 times more efficiently than the widely used P-4(5)-1-(2-nitrophenyl)ethyl-caged IP3 (NPE-IP3). 6-NV-IP3 has a two-photon cross-section of about 0.035 GM at 730 nm. This absorbance is sufficiently large for effective two-photon excitation in living cells at modest power levels. Using near-IR light (5 mW, 710 nm, 80 MHz, pulse-width 70 fs), we produced focal bursts of IP3 in HeLa cells, as revealed by loser-scanning confocal imaging of intracellular Ca2+ concentrations. Therefore, 6-NV-IP3 can be used for efficient, subcellular photorelease of IP3, not only in cultured cells but also, potentially, in vivo. It is in the latter situation that two-photon photolysis should reveal its true forte.

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