One of the main requirements for a 2-D protocol is reproducibility of spot position, and, indeed, the technique of isoelectric focusing on immobilized pH gradients (IPGs) is ideally suited to provide highly reproducible 1-d separations. IPGs are obtained through the copolymerization of acidic and basic acrylamido derivatives of different pKs within a polyacrylamide matrix (1, 2) (Fig. 1). The pH gradient may be devised by computer modeling either with a linear or with an exponential course. IPGs are cast from two limiting solutions containing the buffering chemicals at concentrations adjusted to give the required pH course upon linear mixing. For consistent results, gradient pouring and polymerization are carried out under controlled conditions. The covalent nature of the chemical bonds formed during the polymerization step results in a permanent stability of the pH gradient within the matrix. Conflicting requirements during the focusing procedure prevent any effective use of IPGs into capillary tubes (3): The need to buffer with carrier ampholytes (CAs) the pH extremes caused by the migration of the polymerization catalysts is contrasted by the adverse effects of the electroendosmotic flow brought about by the addition of CAs to the gel phase. The demand for the IPG gels to be backed by a binding support—they are usually cast on GelBond™ foils—results in dimensional stability between 1-D and 2-D as a further assistance to reproducibility.

Casting immobilized pH gradients / E. Gianazza (SPRINGER PROTOCOLS). - In: The Protein Protocols Handbook / [a cura di] J.R. Walker. - Totowa : Humana Press, 2009. - ISBN 9781603274746. - pp. 305-322 [10.1007/978-1-59745-198-7_35]

Casting immobilized pH gradients

E. Gianazza
Primo
2009

Abstract

One of the main requirements for a 2-D protocol is reproducibility of spot position, and, indeed, the technique of isoelectric focusing on immobilized pH gradients (IPGs) is ideally suited to provide highly reproducible 1-d separations. IPGs are obtained through the copolymerization of acidic and basic acrylamido derivatives of different pKs within a polyacrylamide matrix (1, 2) (Fig. 1). The pH gradient may be devised by computer modeling either with a linear or with an exponential course. IPGs are cast from two limiting solutions containing the buffering chemicals at concentrations adjusted to give the required pH course upon linear mixing. For consistent results, gradient pouring and polymerization are carried out under controlled conditions. The covalent nature of the chemical bonds formed during the polymerization step results in a permanent stability of the pH gradient within the matrix. Conflicting requirements during the focusing procedure prevent any effective use of IPGs into capillary tubes (3): The need to buffer with carrier ampholytes (CAs) the pH extremes caused by the migration of the polymerization catalysts is contrasted by the adverse effects of the electroendosmotic flow brought about by the addition of CAs to the gel phase. The demand for the IPG gels to be backed by a binding support—they are usually cast on GelBond™ foils—results in dimensional stability between 1-D and 2-D as a further assistance to reproducibility.
Outlet Tubing; Polymerization Step; Carrier Ampholyte; Molding Plate; Gradient Mixer
Settore BIO/10 - Biochimica
2009
Book Part (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/139759
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