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Arginine functionality

Applications. A biotinylated GOX-based biosensor was developed based on a new electropolymerized material consisting of a pol3rp3uidyl complex of ruthenium(II) functionalized with a pyrrole group [90]. Because histidine, lysine and arginine functions also coordinate Os /Os , biosensors based on co-electrodeposited GOX, HRP, soybean peroxidase (SBP) and laccase with redox Os /Os polymer have been developed [89]. A metal chelate formed by nickel and nitrilotriacetic acid was used to modify a screen-printed electrode surface. The functionalized support allowed stable attachment of acetylcholinesterase and the resulting biosensor was used for sensitive detection of organophosphorus insecticides [91]. This method is attractive because it ensures a controlled and oriented enzyme immobilization, considerably improving the sensitivity and the detection limit. [Pg.502]

Olken, N.M. and Marietta, M.A. (1993) A°-Methyl-L- arginine functions as an alternate substrate and mechanism-based inhibitor of nitric oxide synthase. Biochemistry, 32,9677-9685. [Pg.312]

The use of nanomaterials [545] such as gold nanoparticles and carbon nanotubes increases the sensor surface and enhances analytical detection. The use of PEGylated arginine functionalized magnetic nanoparticles for early detection of cervical cancer has been reported [553]. This sensor displayed good selectivity and sensitively down to 10 cells mL ... [Pg.270]

D. Ma, Q.M. Lin, L.M. Zhang, YY Liang, and W. Xue, A star-shaped porphyrin-arginine functionalized poly(l-lysine) copolymer for photo-enhanced drug and gene co-dehvery. Biomaterials, 35 (14), 4357-67,2014. [Pg.342]

Morris VB, Sharma CP (2010) Folate mediated in vitro targeting of depolymerised trimethy-lated chitosan having arginine functionality. J Colloid Interface Sci 348 360-368... [Pg.20]

Vasopressin and Oxytocin. Arginine -vasopressin (AVP, vasopressia also known as antidiuretic hormone, ADH) (342) is a nonapeptide amide that functions both as a neuroregulator and a hormone (84,85). Oxytocia (OT) (343) is a nonapeptide amide related to AVP. [Pg.578]

Thirty percent of the tumor-derived mutations are in L3, which contains the single most frequently mutated residue, Arg 248. Clearly the interaction between DNA and the specific side chain of an arginine residue inside the minor groove is of crucial importance for the proper function of p53. It is an open question whether this interaction is needed for the recognition of specific DNA sequences, or is required for the proper distortion of the DNA structure, or a combination of both. Other residues that are frequently mutated in this region participate in interactions with loop L2 and stabilize the structures of loops L2 and L3. Mutations of these residues presumably destabilize the structure so that efficient DNA binding can no longer take place. [Pg.171]

All the residues involved in important functions in the catalytic mechanism are strictly conserved in all homologous GTPases with one notable exception. Ras does not have the arginine in the switch 1 region that stabilizes the transition state. The assumption that the lack of this catalytically important residue was one reason for the slow rate of GTP hydrolysis by Ras was confirmed when the group of Alfred Wittinghofer, Max-Planck Institute,... [Pg.260]

Heterocyclic enamines A -pyrroline and A -piperideine are the precursors of compounds containing the pyrrolidine or piperidine rings in the molecule. Such compounds and their N-methylated analogs are believed to originate from arginine and lysine (291) by metabolic conversion. Under cellular conditions the proper reaction with an active methylene compound proceeds via an aldehyde ammonia, which is in equilibrium with other possible tautomeric forms. It is necessary to admit the involvement of the corresponding a-ketoacid (12,292) instead of an enamine. The a-ketoacid constitutes an intermediate state in the degradation of an amino acid to an aldehyde. a-Ketoacids or suitably substituted aromatic compounds may function as components in active methylene reactions (Scheme 17). [Pg.295]

Certain amino acids and their derivatives, although not found in proteins, nonetheless are biochemically important. A few of the more notable examples are shown in Figure 4.5. y-Aminobutyric acid, or GABA, is produced by the decarboxylation of glutamic acid and is a potent neurotransmitter. Histamine, which is synthesized by decarboxylation of histidine, and serotonin, which is derived from tryptophan, similarly function as neurotransmitters and regulators. /3-Alanine is found in nature in the peptides carnosine and anserine and is a component of pantothenic acid (a vitamin), which is a part of coenzyme A. Epinephrine (also known as adrenaline), derived from tyrosine, is an important hormone. Penicillamine is a constituent of the penicillin antibiotics. Ornithine, betaine, homocysteine, and homoserine are important metabolic intermediates. Citrulline is the immediate precursor of arginine. [Pg.87]

FIGURE 5.20 Trypsin is a proteolytic enzyme, or protease, that specifically cleaves only those peptide bonds in which arginine or lysine contributes the carbonyl function. The products of the reaction are a mixture of peptide fragments with C-terminal Arg or Lys residues and a single peptide derived from the polypeptide s C-terminal end. [Pg.135]

The 20 common amino acids can be further classified as neutral, acidic, or basic, depending on the structure of their side chains. Fifteen of the twenty have neutral side chains, two (aspartic acid and glutamic acid) have an extra carboxylic acid function in their side chains, and three (lysine, arginine, and histidine) have basic amino groups in their side chains. Note that both cysteine (a thiol) and tyrosine (a phenol), although usually classified as neutral amino acids, nevertheless have weakly acidic side chains that can be deprotonated in strongly basic solution. [Pg.1021]

Arginine, the most basic of the 20 common amino acids, contains a guanidino functional group in its side chain. Explain, using resonance structures to show how the protonated guanidino group is stabilized. [Pg.1056]


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Arginine functional group

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