Peptides size exclusion HPLC

A method for determination of the aromatic amino acid phenylalanine (45), tyrosine (46) and tryptophan (47) content of peptides at low microgram levels is based on size-exclusion HPLC combined with UVD using a diode array, and data processing of the... 

Note that proteins are now synthesized routinely by stepwise assembly or fragment condensation (see Vol. E22a, Section 4.1 ) 67 68 and chances of product contamination with shorter fragments that may have similar retention times under RP-HPLC should be considered 69 Additionally, size-exclusion HPLC was found to be particularly useful in distinguishing linear from cyclic peptides. 

The three major modes of HPLC employed in peptide separations utilize differences in peptide size (size exclusion HPLC or SEC), net charge (ion-exchange HPLC or lEC), or hydrophobicity (reversed-phase HPLC or RPC). Within these modes, mobile phase conditions may be manipulated to maximize the separation potential of a particular HPLC column. RPC remains by far the... 

Other groups have also used EC and CE to perform non-comprehensive multidimensional separations (15, 16). A three-dimensional separation was performed by Stromqvist in 1994, where size exclusion chromatography (SEC), reverse-phase HPLC, and CZE were used in an off-line manner to separate peptides (17). The most useful information gained from all of these non-comprehensive studies was knowledge of the orthogonality and compatibility of EC and CE. 

Detection in 2DLC is the same as encountered in one-dimensional HPLC. A variety of detectors are presented in Table 5.2. The choice of detector is dependent on the molecule being detected, the problem being solved, and the separation mode used for the second dimension. If MS detection is utilized, then volatile buffers are typically used in the second-dimension separation. Ultraviolet detection is used for peptides, proteins, and any molecules that contain an appropriate chromophore. Evaporative light scattering detection has become popular for the analysis of polymers and surfactants that do not contain UV chromophores. Refractive index (RI) detection is generally used with size exclusion chromatography for the analysis of polymers. 

Aurora Biomolecules dedicates to peptide synthesis (and polyclonal antibody production) for any small quantity purpose. FMOC chemistry (on Perceptive Biosystems Pioneer instruments) is used for peptides synthesis Online monitoring of the coupling efficiencies and HATU activation helps insure that the major component of the synthesis is the correct oligopeptide. Purification is firstly carried out by size exclusion chromatography, and then by HPLC on a PE vision purification workstation. Typically, 20 mg of pure peptide are obtained. The molecular weight of the purified peptide is determined as a final confirmation of quality. 

Figure 9. The effect of storage on protein and peptide composition in cooked ground beef stored in a refrigerator of 4 days (adapted from 7). Upper graph represents the size exclusion chromatography of acidic extracts of fresh, cooked, and cooked-stored beef. Lx)wer graph represents the reverse phase HPLC of peak II from the size exclusion chromatography.

Gonzalez de Llano et al. (47) separated amino acids from low-molecular-weight peptides by means of size-exclusion chromatography on Sephadex G-10, with water as the solvent, as a preparatory step before RP-HPLC analysis of peptides from blue cheeses soluble in 5% PTA (Fig. 1). This technique has also been used (51a) to eliminate the amino acids from the ethanol-... 

Because of their well-recognized physicochemical properties (relatively high hydrophobicity, cationic character, and short length) reversed-phase, size-exclusion, and cation exchange chromatographies are particularly appropriate to purify bioactive peptides from the immune system of invertebrates. The sensitivity of HPLC, MS, Edman degradation, and liquid growth inhibition assays allow one to use from narrow (e.g., 2.1-mm internal diameter) down to micro-or nano-columns. 

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