Gene inactivation by multiphoton-targeted photochemistry

Michael W. Berns, Zifu Wang, Andrew K. Dunn, Vincent Wallace, Vasan Venugopalan

Research output: Contribution to journalArticle

34 Citations (Scopus)

Abstract

Multiphoton-targeted photochemistry was used to selectively inactivate the expression of genes in vertebrate cells. A membrane permeable DNA-associating vital dye, ethidium bromide monoacetate (visible wavelength single photon absorption peak at 530 nm) was used to photosensitize chromosomes in dividing cells. A 100-ps infrared laser beam operating at 1.06 microns was focused onto a selected region of a mitotic chromosome corresponding to the sites of the nucleolar (ribosomal) genes. Individual cells followed through mitosis demonstrated a reduction in the number of nucleoli formed in daughter cells that corresponded to the number of nucleolar genes sites irradiated. These results demonstrate the ability to selectively manipulate genes by using the focal point specificity characteristic of multiphoton microscopy. This technique should have wide biotechnology applications both in vitro and in vivo.

Original languageEnglish
Pages (from-to)9504-9507
Number of pages4
JournalProceedings of the National Academy of Sciences of the United States of America
Volume97
Issue number17
Publication statusPublished - 15 Aug 2000
Externally publishedYes

Fingerprint Dive into the research topics of 'Gene inactivation by multiphoton-targeted photochemistry'. Together they form a unique fingerprint.

Cite this