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Functional group targets proteins

As seen in the previous work, arsenic will bind to biological molecules and hinder enzymic activity. The main mode of action seems to be to bind to systems that contain thiol as a functional group. For proteins, this can be either cysteine or cofactors that contain thiol groups. Our recent research efforts have elucidated the interaction with some of the target molecules. The arsenical that we have used is phenyldichloroarsine, an organic trivalent species that can penetrate cells easily. [Pg.700]

Following reports [22,27], various PEG derivatives endowed with high reactivity toward target functional groups of protein molecule were developed, as shown in Fig. 3. Some of them are commercially available from Shearwater Polymers, Inc. (Huntsville, AL), Sigma Chemical Co. (St. Louis, MO), and others. [Pg.715]

Schemes are available, however, that start from the free carboxylic acid, plus an activator . Dicyclohexylcarbodiimide, DCC, has been extensively employed as a promoter in esterification reactions, and in protein chemistry for peptide bond formation [187]. Although the reagent is toxic, and a stoichiometric concentration or more is necessary, this procedure is very useful, especially when a new derivative is targeted. The reaction usually proceeds at room temperature, is not subject to steric hindrance, and the conditions are mild, so that several types of functional groups can be employed, including acid-sensitive unsaturated acyl groups. In combination with 4-pyrrolidinonepyridine, this reagent has been employed for the preparation of long-chain fatty esters of cellulose from carboxylic acids, as depicted in Fig. 5 [166,185,188] ... Schemes are available, however, that start from the free carboxylic acid, plus an activator . Dicyclohexylcarbodiimide, DCC, has been extensively employed as a promoter in esterification reactions, and in protein chemistry for peptide bond formation [187]. Although the reagent is toxic, and a stoichiometric concentration or more is necessary, this procedure is very useful, especially when a new derivative is targeted. The reaction usually proceeds at room temperature, is not subject to steric hindrance, and the conditions are mild, so that several types of functional groups can be employed, including acid-sensitive unsaturated acyl groups. In combination with 4-pyrrolidinonepyridine, this reagent has been employed for the preparation of long-chain fatty esters of cellulose from carboxylic acids, as depicted in Fig. 5 [166,185,188] ...
Covalent attachment of proteins to the surface of liposomal bilayers is done through reactive sites created on the head groups of phospholipids with the intermediary use of a crosslinker or other activating agent. The lipid functional groups described in Section 1 of this chapter are modified according to the methods discussed in Section 2 to be reactive toward specific target... [Pg.885]


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See also in sourсe #XX -- [ Pg.3 ]

See also in sourсe #XX -- [ Pg.3 ]




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Functional group targets

Functional group targets groups

Functional protein-functionalized

Functional targets Proteins

Functionality protein

Protein functional groups

Protein target

Protein targeting

Protein targeting proteins)

Proteins functioning

Proteins groups

Proteins targeted

Target function

Target group

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