Electrochemical and spectrophotometric studies on dyes and proteins labelled with dyes
(2005) In Synthetic Metals 155(2). p.426-429- Abstract
- Electrochemical and fluorometric studies on a few selected phenazine and phenoxazine dyes has been carried out in free conditions and when covalently attached to a protein. The dyes have been coupled using the conventional coupling agent carbodiimide (derivative). Neutral Red and Nile Blue A, show significant shifts in their emission peaks to shorter wavelengths on binding to bovine serum albumin (BSA). Phenazine dyes such as Safranine O and Neutral Red show a shift in their formal redox potential to more positive potential on binding to BSA along with the two electron transfers taking place in a single step unlike incase of the free dyes where the two electron transfers take place at different potentials. Nile Blue A shows a negative... (More)
- Electrochemical and fluorometric studies on a few selected phenazine and phenoxazine dyes has been carried out in free conditions and when covalently attached to a protein. The dyes have been coupled using the conventional coupling agent carbodiimide (derivative). Neutral Red and Nile Blue A, show significant shifts in their emission peaks to shorter wavelengths on binding to bovine serum albumin (BSA). Phenazine dyes such as Safranine O and Neutral Red show a shift in their formal redox potential to more positive potential on binding to BSA along with the two electron transfers taking place in a single step unlike incase of the free dyes where the two electron transfers take place at different potentials. Nile Blue A shows a negative shift in the reduction peak on covalently binding to BSA. These dyes when covalently coupled to the proteins mediate intramolecular electron transfers. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/157154
- author
- Salomi, B S B ; Mitra, C K and Gorton, Lo LU
- organization
- publishing date
- 2005
- type
- Contribution to journal
- publication status
- published
- subject
- in
- Synthetic Metals
- volume
- 155
- issue
- 2
- pages
- 426 - 429
- publisher
- Elsevier
- external identifiers
-
- wos:000234150000046
- scopus:28544450300
- ISSN
- 0379-6779
- DOI
- 10.1016/j.synthmet.2005.09.029
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Analytical Chemistry (S/LTH) (011001004)
- id
- 06a785a3-4e19-41e9-8e71-eec02f14c664 (old id 157154)
- date added to LUP
- 2016-04-01 16:36:25
- date last changed
- 2025-04-04 14:25:52
@article{06a785a3-4e19-41e9-8e71-eec02f14c664,
abstract = {{Electrochemical and fluorometric studies on a few selected phenazine and phenoxazine dyes has been carried out in free conditions and when covalently attached to a protein. The dyes have been coupled using the conventional coupling agent carbodiimide (derivative). Neutral Red and Nile Blue A, show significant shifts in their emission peaks to shorter wavelengths on binding to bovine serum albumin (BSA). Phenazine dyes such as Safranine O and Neutral Red show a shift in their formal redox potential to more positive potential on binding to BSA along with the two electron transfers taking place in a single step unlike incase of the free dyes where the two electron transfers take place at different potentials. Nile Blue A shows a negative shift in the reduction peak on covalently binding to BSA. These dyes when covalently coupled to the proteins mediate intramolecular electron transfers.}},
author = {{Salomi, B S B and Mitra, C K and Gorton, Lo}},
issn = {{0379-6779}},
language = {{eng}},
number = {{2}},
pages = {{426--429}},
publisher = {{Elsevier}},
series = {{Synthetic Metals}},
title = {{Electrochemical and spectrophotometric studies on dyes and proteins labelled with dyes}},
url = {{http://dx.doi.org/10.1016/j.synthmet.2005.09.029}},
doi = {{10.1016/j.synthmet.2005.09.029}},
volume = {{155}},
year = {{2005}},
}