A Fluorescent-Photochrome Method for the Quantitative Characterization of Solid Phase Antibody Orientation
β Scribed by Arti Ahluwalia; Danilo De Rossi; Giuseppe Giusto; Oren Chen; Vladislav Papper; Gertz I. Likhtenshtein
- Publisher
- Elsevier Science
- Year
- 2002
- Tongue
- English
- Weight
- 251 KB
- Volume
- 305
- Category
- Article
- ISSN
- 0003-2697
No coin nor oath required. For personal study only.
β¦ Synopsis
A fluorescent-photochrome method of quantifying the orientation and surface density of solid phase antibodies is described. The method is based on measurements of quenching and rates of cis-trans photoisomerization and photodestruction of a stilbene-labeled hapten by a quencher in solution. These experimental parameters enable a quantitative description of the order of binding sites of antibodies immobilized on a surface and can be used to characterize the microviscosity and steric hindrance in the vicinity of the binding site. Furthermore, a theoretical method for the determination of the depth of immersion of the fluorescent label in a two-phase system was developed. The model exploits the concept of dynamic interactions and is based on the empirical dependence of parameters of static exchange interactions on distances between exchangeable centers. In the present work, anti-dinitrophenyl (DNP) antibodies and stilbene-labeled DNP were used to investigate three different protein immobilization methods: physical adsorption, covalent binding, and the Langmuir-Blodgett technique.
π SIMILAR VOLUMES
A solid-phase radioimmunoassay for the detection of anti-ribosome antibodies is described. Only small quantities of ribosomal particles are required, and low levels of antibody can be detected by very simple procedures. This assay has been used to detect antibodies which bind to intact ribosomes and
Two general methods for labeling synthetic peptides with a 5-dimethylamino-1-napthalenesulfonyl idansyl) group at the C-terminal residue using solid phase peptide synthesis (SPPS) are described. Dansylated peptides are ideal substrates for fluorometric proteolytic enzyme assays.
Abstrnctr A general method for the solid-phase synthesis of ureas has been developed. The key intermediate being a p-nitrophenylcarbamate which is transformed into the urea by reaction with primary or secondary amines. The products obtained are of high chemical purity. The generation of molecular d