Determination of the cysteine residues in the surface-confined biomolecules by using electrochemical desorption and fluorescence detection.
- Author:
Li-Juan WU
1
;
Jian-Xiu WANG
;
Kai LI
;
Mao-Tian XU
Author Information
1. School of Chemistry and Chemical Engineering, Central South University, Changsha 410083, China.
- Publication Type:Journal Article
- MeSH:
Biosensing Techniques;
methods;
Cysteine;
analysis;
Electrochemistry;
methods;
Fluorescence;
Glutathione;
analysis;
chemistry;
Maleimides;
chemistry;
Oligodeoxyribonucleotides;
analysis;
Reproducibility of Results;
Sensitivity and Specificity
- From:
Acta Pharmaceutica Sinica
2008;43(1):86-90
- CountryChina
- Language:Chinese
-
Abstract:
To develop a method for the detection of surface-confined peptides containing cysteine residues or oligodeoxynucleotides (ODNs) whose 3' ends modified with thiol groups, and a thiol-specific fluorescent cross-linker, N-(9-acridinyl) maleimide (NAM) was used. The peptides studied herein include both the oxidized and reduced forms of glutathione, and a hexapeptide (FT). Peptides are first attached onto the activated 11-mercaptoundecanoic acid (MUA)-terminated alkanethiol self-assembled monolayers (SAMs) and then derivatized with NAM. The cysteine residues was determined by using electrochemical desorption and fluorescence detection. GSH concentration as low as 40 pmol x L(-1) can be measured. The fluorescence intensity in the case of FT is about 3 times as high as that for GSH, which is consistent with the molar ratio of cysteine residues in these two molecules. The analytical performance of gene analysis was also evaluated through the analyses of a complementary target and targets with varying numbers of mismatching bases. The method described here is simple, sensitive, reproducible, and does not require sophisticated analytical instrumentation and separation procedures.
