Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Cross-linking reagent, cleavable

Denney, J.B., and Blobel, G. (1984) 1251-Labeled cross-linking reagent that is hydrophilic, photoactivat-able, and cleavable through an azo linkage. Proc. Natl. Acad. Sci. USA 81, 5286-5290. [Pg.1058]

Jaffe, C.L., Lis, H., and Sharon, N. (1980) New cleavable photoreactive heterobifunctional cross-linking reagents for studying membrane organization. Biochemistry 19, 4423. [Pg.1078]

Lomant, A.J., and Fairbanks, G. (1976) Chemical probes of extended biological structures synthesis and properties of the cleavable cross-linking reagent [35S] dithiobis(succinimidyl propionate)./. Mol. Biol. 104, 243-261. [Pg.1089]

Traut RR, Bollen A, Sun TT et al (1973) Methyl 4-mercaptobutyrimidate as a cleavable cross-linking reagent and its application to the Escherichia coli 30s ribosome. Biochemistry 12 3266-3273... [Pg.279]

Abdella, R.M., Smith, P.K., and Royer, G.P. (1979) A new cleavable reagent for cross-linking and reversible immobilization of proteins. Biochem. Biophys. Res. Comm. 87, 734-742. [Pg.1041]

Sato, S., and Nakao, M. (1981) Cross-linking of intact erythrocyte membrane with a newly synthesized cleavable bifunctional reagent./. Biochem. (Tokyo) 90, 1177. [Pg.1110]

Smith, R.J., Capaldi, R.A., Muchmone, D., and Dahlquist, F. (1978) Cross-linking of ubiquinone cytoch-nome c reductase (complex III) with periodate-cleavable bifunctional reagents. Biochemistry 17, 3719-3723. [Pg.1116]

Figure 193 The trifunctional reagent sulfo-SBED reacts with amine-containing molecules via its NHS ester side chain. Subsequent exposure to UV light can cause cross-link formation with a second interacting molecule. The biotin portion provides purification or labeling capability using avidin or streptavidin reagents. The disulfide bond on the NHS ester arm provides cleavability using disulfide reductants. Figure 193 The trifunctional reagent sulfo-SBED reacts with amine-containing molecules via its NHS ester side chain. Subsequent exposure to UV light can cause cross-link formation with a second interacting molecule. The biotin portion provides purification or labeling capability using avidin or streptavidin reagents. The disulfide bond on the NHS ester arm provides cleavability using disulfide reductants.
Control experiments showed that all the crosslinks were cleavable. No crosslinks were formed if the reagent was omitted, if photolysis was omitted, or if the reagent was first inactivated by treatment with ammonium acetate. These experiments proved that neither monofunctional cross-linking, nor disulfide interchange to give crosslinking in the dark occurred. If the membranes were solubilized in SDS before irradiation no cross-... [Pg.136]


See other pages where Cross-linking reagent, cleavable is mentioned: [Pg.447]    [Pg.1122]    [Pg.194]    [Pg.38]    [Pg.40]    [Pg.218]    [Pg.229]    [Pg.196]    [Pg.198]    [Pg.209]    [Pg.79]    [Pg.104]    [Pg.105]    [Pg.105]    [Pg.106]    [Pg.262]    [Pg.212]    [Pg.213]    [Pg.234]    [Pg.284]    [Pg.292]    [Pg.312]    [Pg.312]    [Pg.55]    [Pg.209]    [Pg.219]    [Pg.192]    [Pg.193]    [Pg.214]    [Pg.264]    [Pg.272]    [Pg.292]   
See also in sourсe #XX -- [ Pg.104 , Pg.105 ]




SEARCH



Cleavability

Cross-linking reagents

Linking reagents

© 2024 chempedia.info