By D. Scott Linthicum, Nadir R. Farid
Here is an updated evaluation of significant new tools and leads to anti-idiotypes, receptors, and molecular mimicry.It starts off with a dialogue of the theoretical historical past ofthe anti-idiotypic community, it is function within the law of immune reaction, and the actual features of anti-idiotypic antibodies. It then is going directly to discover many exciting purposes in such parts as insulin motion, thyroid cellphone functionality, the neurosciences, cardiology, virology, pharmacology, and copy.
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1) (0) or the outer cavity sites (A and B in Fig. 4. 1) (0 ) . 9 was determined by competitive EIA and compared to the competitive binding of noncomplexed Mcg (D). 30 Robert L. Raison and Allen B. B. , unpublished work). After prolonged incubation with hapten, the complex was dialyzed to remove bis(DNP)lysine from the main cavity. The ligand in the deep pocket remained firmly bound. 0 mole of bis(DNP)lysine per mole of Mcg dimer, as determined by absorbance at 365 nm. This preparation showed a markedly reduced ability to bind the M3.
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C. Ellory. and G. Dawson. 1983. Molecular size of opiate (enkephalin) receptors in neuroblastoma-glioma hybrid cells as determined by radiation inactivation analysis. J. BioI. Chern. 258:2101. II. • S. L. M. J. Simon. 1985. Covalent labeling of opioid receptors with radioiodinated human b-endorphin. J. BioI. Chern. 260: 10833. 12. F. W. R. E. c. Rice. 1982. Identification of aM, 58000 glycoprotein subunit of the opiate receptor. FEBS Lett. 150: 125. 13. D. D. L. E. Blalock. 1986. Antibodies to the binding site of the LHRH receptor: generation with a synthetic decapeptide encoded by a RNA complementary to LHRH mRNA.
Anti-Idiotypes, Receptors, and Molecular Mimicry by D. Scott Linthicum, Nadir R. Farid