Albumin charge

When assessing any variation in albumin charge induced by browning one should consider that at least three relevant phenomena may take place 1) glycosylation of... 

Preparation of nanoparticles can be by a variety of different ways. The most important and frequently used is emulsion polymerization others include interfacial polymerization, solvent evaporation, and desolvation of natural proteins. The materials used to prepare nanoparticles are also numerous, but most commonly they are polymers such as poly-alklcyanoacrylate, polymethylmethacrylate, poly-butylcyanoacrylate, or are albumin or gelatin. Distribution patterns of the particles in the body can vary depending on their size, composition, and surface charge [83-85]. In particular, nanoparticles of polycyanoacrylate have been found to accumulate in certain tumors [86,87]. 

Jansen RW, Schols D, Pauwels R, De Clercq E, Meijer DKF. Novel, negatively charged, human serum albumins display potent and selective in vitro anti-human immunodeficiency virus type 1 activity. Mol Pharmacol 1993 44 1003-1007. 

Gelamo and Tabak (2000) reported a dramatic decrease in the binding of SDS to reduced bovine serum albumin at pH 9.0 compared to pH 7.0. However, this phenomenon is expected only if disulfide bonds are reduced there is little difference in the charge of the protein at these two pHs if the disulfide bonds are intact. 

Fig. 6. Plateau-values, I"P1 /mg m 2, of adsorption isotherms of lysozyme (LSZ), ribonuclease (RNase), a -lactalbumin (aLA), calcium-depleted (X -lactalbumin (aLA(-Ca )) and bovine serum albumin (BSA) on hydrophobic polystyrene (PS) and hydrophilic hematite (a — Fe203) and silica (Si02) surfaces. An indication of the charge density of the surface is given by the zeta-potential, C, and of the proteins by + and signs. Ionic strength 0.05 M T = 25°C. (Derived from Currie et al. 2003).

Even complicated, charged macromolecules like proteins can be succesfully displaced. As an example we give in Figure 6 the displacement isotherm for human plasma albumin from silica by morpholine (21). Of course, in this case where charge effects and a variety of segment/surface interactions play a role, our simple Equation 5 does not apply. Nevertheless, for practical work it is important to realize that most macromolecules, often thought to be irreversibly adsorbed, can be removed completely from the adsorbent surface by the concerted action of a large number of small molecules. 

Figure 6.4. Fragmentation spectrum of a tryptic peptide obtained from bovine serum albumin. Peptide sequence LGEYGFQNALIVR, monoisotopic [M + H]+ = 1479.796, monoisotopic [M+2H]2+ =740.402. Upper panel full scan MS spectrum. Lower panel MS/MS spectrum of a doubly-charged ion at 740.7 m/z with a ladder of y ions, the distances between which correspond to amino acid residues (upper row of letters). A shorter series of b ions is also seen (lower row of letters). See Fig. 6.5 for description of nomenclature. Note the often observed phenomenon where multiply-charged ions lose the charge during fragmentation process and, therefore, have higher m/z values than the original parent ion.

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