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Quantitative Comparison of Long-wavelength Alexa Fluor Dyes to Cy Dyes: Fluorescence of the Dyes and Their Bioconjugates

Berlier, Judith E., Rothe, Anca, Buller, Gayle, Bradford, Jolene, Gray, Diane R., Filanoski, Brian J., Telford, William G., Yue, Stephen, Liu, Jixiang, Cheung, Ching-Ying, Chang, Wesley, Hirsch, James D., Beechem Rosaria P. Haugland, Joseph M., Haugland, Richard P.·2003·Journal of Histochemistry & Cytochemistry

Abstract

Amine-reactive N-hydroxysuccinimidyl esters of Alexa Fluor fluorescent dyes with principal absorption maxima at about 555 nm, 633 nm, 647 nm, 660 nm, 680 nm, 700 nm, and 750 nm were conjugated to antibodies and other selected proteins. These conjugates were compared with spectrally similar protein conjugates of the Cy3, Cy5, Cy5.5, Cy7, DY-630, DY-635, DY-680, and Atto 565 dyes. As N-hydroxysuccinimidyl ester dyes, the Alexa Fluor 555 dye was similar to the Cy3 dye, and the Alexa Fluor 647 dye was similar to the Cy5 dye with respect to absorption maxima, emission maxima, Stokes shifts, and extinction coefficients. However, both Alexa Fluor dyes were significantly more resistant to photobleaching than were their Cy dye counterparts. Absorption spectra of protein conjugates prepared from these dyes showed prominent blue-shifted shoulder peaks for conjugates of the Cy dyes but only minor shoulder peaks for conjugates of the Alexa Fluor dyes. The anomalous peaks, previously observed for protein conjugates of the Cy5 dye, are presumably due to the formation of dye aggregates. Absorption of light by the dye aggregates does not result in fluorescence, thereby diminishing the fluorescence of the conjugates. The Alexa Fluor 555 and the Alexa Fluor 647 dyes in protein conjugates exhibited significantly less of this self-quenching, and therefore the protein conjugates of Alexa Fluor dyes were significantly more fluorescent than those of the Cy dyes, especially at high degrees of labeling. The results from our flow cytometry, immunocytochemistry, and immunohistochemistry experiments demonstrate that protein-conjugated, long-wavelength Alexa Fluor dyes have advantages compared to the Cy dyes and other long-wavelength dyes in typical fluorescence-based cell labeling applications.

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Metadata

Authors
Berlier, J. E., Rothe, A., Buller, G., Bradford, J., Gray, D. R., Filanoski, B. J., Telford, W. G., Yue, S., Liu, J., Cheung, C.-Y., Chang, W., Hirsch, J. D., Beechem Rosaria P. Haugland, J. M., & Haugland, R. P.
Venue
Journal of Histochemistry & Cytochemistry
Published
2003-12
Volume
51
Issue
12
Pages
1699-1712
ISSN
  • 0022-1554 (ISSN-L)
  • 1551-5044
OpenAlex
W2152043216
Cited by
379
References
15
FWCI
5.01
Type
journal article
Language
en
Open access
closed

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Berlier, J. E., Rothe, A., Buller, G., Bradford, J., Gray, D. R., Filanoski, B. J., Telford, W. G., Yue, S., Liu, J., Cheung, C.-Y., Chang, W., Hirsch, J. D., Beechem Rosaria P. Haugland, J. M., & Haugland, R. P. (2003). Quantitative Comparison of Long-wavelength Alexa Fluor Dyes to Cy Dyes: Fluorescence of the Dyes and Their Bioconjugates. Journal of Histochemistry & Cytochemistry. https://doi.org/10.1177/002215540305101214

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