On-line capillary zone electrophoresis/electrospray ionization mass spectrometry (CZE-ESMS) and capillary isoelectric focusing/electrospray ionization mass spectrometry (CIEF/ESMS) were employed for protein analysis. The separation mechanisms and the detection limits of CZE/ESMS and CIEF/ESMS were c
Protocol of capillary isoelectric focusing to separate extremely acidic and basic proteins
β Scribed by Chun Yang; Weibing Zhang; Jie Zhang; Jicheng Duan; Yukui Zhang
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- English
- Weight
- 330 KB
- Volume
- 28
- Category
- Article
- ISSN
- 1615-9306
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β¦ Synopsis
A new set-up was constructed for capillary isoelectric focusing (CIEF) involving a sampling capillary as a bypass fixed to the separation capillary. Sample solutions were subjected to a previously established pH gradient from the sample capillary. Besides performing conventional CIEF, the separation of ampholytic compounds with isoelectric points (p/s) beyond the pH gradient was carried out on this system. This method was termed as pH gradient driven electrophoresis (PGDE) and the basic mathematical expressions were derived to express the dynamic fundamentals. Proteins such as lysozyme, cytochrome C, and pepsin with p/s higher than 10 or below 3 were separated in a pH gradient provided by Pharmalyte (pH 3-10). Finally, this protocol convincingly exhibited its potential in the separation of a solution of chicken egg white.
π SIMILAR VOLUMES
The substances to be separated must have an isoelectric point at which they are not charged.
A novel on-line 2-D system was developed for peptide and protein mapping. The system combines capillary IEF (cIEF) with pressurized CEC (pCEC) using a micro-injection valve as the interface. Sample fractions, which were focused and separated in the firstdimension cIEF based on their differences in p
## Abstract A comprehensive twoβdimensional (2βD) separation system, coupling capillary reverseβphase liquid chromatography (cRPLC) to capillary isoelectric focusing (CIEF), is described for protein and peptide mapping. cRPLC, the first dimension, provided highβresolution separations for saltβfree
## Abstract This report describes a method for enrichment and separation of acidic and basic proteins using the centrifugal ultrafiltration followed by nanoparticleβfilled capillary electrophoresis. To improve stacking and separation efficiencies of proteins, the separation buffer containing 1.6% p