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Arginine-Reactive and Photoreactive Crosslinkers

ASBA has been used to identify parasite adhesive proteins (Gowda et al., 2007), for active site-directed labeling of glucosidase I (Romaniouk et al., 2004), and to study interactions with the proteasome (Qureshi et al., 2003). [Pg.333]

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.334]

p-azidophcnyl glyoxal, is a heterobifunctional crosslinker containing an arginine-specific diketone group on one end and a photosensitive phenyl azide group on the other end (Thermo [Pg.334]

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 or affinity interaction. [Pg.336]


See other pages where Arginine-Reactive and Photoreactive Crosslinkers is mentioned: [Pg.333]    [Pg.333]    [Pg.335]   


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Crosslinkers photoreactive

Reactive and Photoreactive Crosslinkers

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