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Reverse isoelectric focusing procedure resolves charge variants of basic proteins.
Anal Biochem. 1995 Aug 10; 229(2):203-6.AB

Abstract

Several powerful methods exist which effectively resolve proteins based on their differences in overall change. Among these, two-dimensional gel electrophoresis, a method combining isoelectric focusing with sodium dodecyl sulfate-polyacrylamide gel electrophoresis, can resolve over 1000 proteins with isoelectric points in the range of pH 4-7. However, resolution of basic proteins is poor, even when the pH gradient is extended to a higher pH. Nonequilibrium pH gradient electrophoresis was developed as an alternative procedure to resolve basic proteins. However, samples must be dissolved in urea prior to analysis and this method requires 2000-8000 V-h for optimal resolution. In this report we demonstrate that a simple, rapid procedure, based on nonequilibrium pH gradient electrophoresis, can resolve the single charge variants of two fungal enzymes with isoelectric points greater than 8. This procedure utilizes ready-made materials and requires less than 500 V-h to complete (total run time is less than 2 h).

Authors+Show Affiliations

Department of Protein Chemistry, Novo Nordisk Biotech, Inc., Davis, California 95616, USA.

Pub Type(s)

Journal Article

Language

eng

PubMed ID

7485973

Citation

Madden, M S.. "Reverse Isoelectric Focusing Procedure Resolves Charge Variants of Basic Proteins." Analytical Biochemistry, vol. 229, no. 2, 1995, pp. 203-6.
Madden MS. Reverse isoelectric focusing procedure resolves charge variants of basic proteins. Anal Biochem. 1995;229(2):203-6.
Madden, M. S. (1995). Reverse isoelectric focusing procedure resolves charge variants of basic proteins. Analytical Biochemistry, 229(2), 203-6.
Madden MS. Reverse Isoelectric Focusing Procedure Resolves Charge Variants of Basic Proteins. Anal Biochem. 1995 Aug 10;229(2):203-6. PubMed PMID: 7485973.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Reverse isoelectric focusing procedure resolves charge variants of basic proteins. A1 - Madden,M S, PY - 1995/8/10/pubmed PY - 1995/8/10/medline PY - 1995/8/10/entrez SP - 203 EP - 6 JF - Analytical biochemistry JO - Anal Biochem VL - 229 IS - 2 N2 - Several powerful methods exist which effectively resolve proteins based on their differences in overall change. Among these, two-dimensional gel electrophoresis, a method combining isoelectric focusing with sodium dodecyl sulfate-polyacrylamide gel electrophoresis, can resolve over 1000 proteins with isoelectric points in the range of pH 4-7. However, resolution of basic proteins is poor, even when the pH gradient is extended to a higher pH. Nonequilibrium pH gradient electrophoresis was developed as an alternative procedure to resolve basic proteins. However, samples must be dissolved in urea prior to analysis and this method requires 2000-8000 V-h for optimal resolution. In this report we demonstrate that a simple, rapid procedure, based on nonequilibrium pH gradient electrophoresis, can resolve the single charge variants of two fungal enzymes with isoelectric points greater than 8. This procedure utilizes ready-made materials and requires less than 500 V-h to complete (total run time is less than 2 h). SN - 0003-2697 UR - https://www.unboundmedicine.com/medline/citation/7485973/Reverse_isoelectric_focusing_procedure_resolves_charge_variants_of_basic_proteins_ L2 - https://linkinghub.elsevier.com/retrieve/pii/S0003-2697(85)71403-0 DB - PRIME DP - Unbound Medicine ER -