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Arginine-Reactive and Photoreactive Cross-linkers

The ability to direct conjugation or modification specifically through arginine residues using this chemistry has been exploited in the availability of the only photoreactive glyoxal derivative, APG. [Pg.285]

APG has been used to inhibit bovine heart lactic dehydrogenase, egg white lysozyme, horse liver alcohol dehydrogenase, and yeast alcohol dehydrogenase (Ngo etal., 1981), in cross-linking RNA—protein interactions in . coli ribosomes (Politz et al., 1981), and in identifying regions of brome mosaic virus coat protein chemically cross-linked in situ to viral RNA (Sgro et al., 1986). [Pg.286]

A convenient molecule from which to build trifunctionals is the amino acid L-lysine. Its three functional groups, a-carboxy, a-amino, and e-amino, can be derivatized independently to contain three arms. Each arm can be designed to terminate in a complexing group able to participate in a particular type of conjugation reaction. [Pg.287]


See other pages where Arginine-Reactive and Photoreactive Cross-linkers is mentioned: [Pg.304]    [Pg.305]    [Pg.284]    [Pg.285]   


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Cross reactivity

Cross-linker

Photoreactive cross-linkers

Reactive and Photoreactive Cross-linkers

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