Characterization of one-and two-photon photochemical uncaging efficiency

Methods in Molecular Biology

Volumn 995, Issue , 2013, Pages 79-87

  Specht, Alexandre ^a   Bolze, Frederic ^a   Nicoud, Jean Francois ^a   Goeldner, Maurice ^a  

^a CNRS   (France)

Author keywords

Photolabile protecting groups; Photolysis; Quantum yield; Two photon; Uncaging

Indexed keywords

ACETONITRILE; AZOBENZENE; FLUORESCEIN; LIQUID NITROGEN; METHANOL; PHOSPHATE BUFFERED SALINE; SILICON DIOXIDE;

ANALYTIC METHOD; AQUEOUS SOLUTION; ARTICLE; ELUTION; FLOW RATE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; IRRADIATION; LIGHT ABSORPTION; LIGHT EXPOSURE; LINEAR REGRESSION ANALYSIS; ONE PHOTON PHOTOCHEMICAL UNCAGING; OPTICAL DENSITY; PHOTOCHEMISTRY; PHOTODEGRADATION; PHOTOLYSIS; PRIORITY JOURNAL; QUANTUM YIELD; ROOM TEMPERATURE; SPECTROPHOTOMETER; TWO PHOTON PHOTOCHEMICAL UNCAGING;

AZO COMPOUNDS; BUFFERS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; LIGHT; PHOTOLYSIS; PHOTONS; QUANTUM THEORY; REFERENCE STANDARDS; SPECTRUM ANALYSIS;

EID: 84877044407     PISSN: 10643745     EISSN: None     Source Type: Book Series    
DOI: 10.1007/978-1-62703-345-9_6     Document Type: Article

References (13)

1. Engels J, Schlaeger EJ (1977) Synthesis, structure, and reactivity of adenosine cyclic 3′ ,5′ -phosphate benzyl triesters. J Med Chem 20(7):907-911
2. Kaplan JH, Forbush B, Hoffman JF (1978) Rapid photolytic release of adenosine 5′ -triphosphate from a protected analogue: utilization by the Na:K pump of human red blood cell ghosts. Biochemistry 17(10):1929-1935
3. Bochet C (2002) Photolabile protecting groups and linkers. J Chem Soc Perkin Trans 1(2):125-152
4. Klan P, Solomek T, Bochet C, Blanc A, Givens R, Rubina M, Popik V, Kostikov A, Wirz J (2013) Photoremovable protecting groups in chemistry and biology: reaction mechanisms and ef ficacy. Chem Rev 115(1):119-191
5. Marriott G (ed) (1998) Caged compounds. Methods in enzymology, vol 291. Academic, New York
6. Goeldner M, Givens R (eds) (2005) Dynamic studies in biology, phototriggers, photoswitches and caged biomolecules. Wiley-VCH, Weinheim
7. Mayer G, Heckel A (2006) Biologically active molecules with a 'light switch'. Angew Chem Int Ed Engl 45(30):4900-4921
8. Ellis-Davies GC (2007) Caged compounds: photorelease technology for control of cellular chemistry and physiology. Nat Methods 4(8): 619-628
9. Lee HM, Larson DR, Lawrence DS (2009) Illuminating the chemistry of life: design, synthesis, and applications of "caged" and related photoresponsive compounds. ACS Chem Biol 4(6):409-427
10. Specht A, Bolze F, Omran Z, Nicoud JF, Goeldner M (2009) Photochemical tools to study dynamic biological processes. HFSP J 3(4):255-264
11. Brieke C, Rohrbach F, Gottschalk A, Mayer G, Heckel A (2012) Light-controlled tools. Angew Chem Int Ed Engl 51(34): 8446-8476
12. Kuhn HJ, Bralavsky SE, Schmidt R (1989) Chemical actinometry. Pure Appl Chem 61(2): 187-210
13. Furuta T, Wang SS, Dantzker JL, Dore TM, Bybee WJ, Callaway EM, Denk W, Tsien RY (1999) Brominated 7-hydroxycoumarin-4-ylmethyls: photolabile protecting groups with biologically useful cross-sections for two photon photolysis. Proc Natl Acad Sci U S A 96: 1193-1200