Literature DB >> 10528153

Chromophore-assisted laser inactivation (CALI) to elucidate cellular mechanisms of cancer.

D G Jay1, T Sakurai.   

Abstract

Chromophore-assisted laser inactivation (CALI) is a new technology for acute protein inactivation in living cells. It targets laser energy to specific proteins via non-function-blocking antibodies that are labeled with the dye malachite green. Excitation of the dye generates short-lived free radicals that damage the bound protein without affecting other cellular components. The wavelength of laser light used (620 nm) is not readily absorbed by cells such that non-specific light damage does not occur. CALI provides an alternative to other inactivation strategies and has the advantages of high spatial and temporal resolution. The ultimate value of this technology for cancer research will be assessed by how effective CALI is in ascribing in situ function during cancer-relevant processes and in identifying and validating protein targets for drug discovery. Recent work using CALI on ezrin and pp60-c-src, two proteins that may be involved in cancer, suggests its potential. Further application of CALI will likely be of utility for understanding cellular mechanisms of cancer and developing cancer therapeutics.

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Year:  1999        PMID: 10528153     DOI: 10.1016/s0304-419x(99)00022-0

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  5 in total

1.  Selective cell targeting with light-absorbing microparticles and nanoparticles.

Authors:  Costas M Pitsillides; Edwin K Joe; Xunbin Wei; R Rox Anderson; Charles P Lin
Journal:  Biophys J       Date:  2003-06       Impact factor: 4.033

2.  Irradiation-induced protein inactivation reveals Golgi enzyme cycling to cell periphery.

Authors:  Timothy Jarvela; Adam D Linstedt
Journal:  J Cell Sci       Date:  2012-03-15       Impact factor: 5.285

Review 3.  Chromophore-assisted laser inactivation in neural development.

Authors:  Wei Li; Nico Stuurman; Guangshuo Ou
Journal:  Neurosci Bull       Date:  2012-08       Impact factor: 5.203

Review 4.  Profiling distinct mechanisms of tumour invasion for drug discovery: imaging adhesion, signalling and matrix turnover.

Authors:  Neil O Carragher
Journal:  Clin Exp Metastasis       Date:  2008-10-29       Impact factor: 5.150

5.  Complementation and reconstitution of fluorescence from circularly permuted and truncated green fluorescent protein.

Authors:  Yao-ming Huang; Christopher Bystroff
Journal:  Biochemistry       Date:  2009-02-10       Impact factor: 3.162

  5 in total

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