Synthetic, structural and biological studies of the ubiquitin system: the total chemical synthesis of ubiquitin
- 1 April 1994
- journal article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 299 (1) , 151-158
- https://doi.org/10.1042/bj2990151
Abstract
The small protein ubiquitin (76 amino acids) has been synthesized under optimized conditions by Merrifield solid-phase methodology using the N alpha-Fmoc protecting group. The crude polypeptide mixture was purified to homogeneity by gel filtration, dialysis and a combination of cation- and anion-exchange chromatography to yield ubiquitin. Amino acid analysis, enzymic digestion and sequencing by automated Edman degradation were used to authenticate the primary structure. Isoelectric focusing and m.s. were used to demonstrate that the final product was greater than 98% pure with a final yield of 93 mg (4.3%) from a single synthesis on a 0.25 nmol scale.Keywords
This publication has 28 references indexed in Scilit:
- Synthetic, structural and biological studies of the ubiquitin system: chemically synthesized and native ubiquitin fold into identical three-dimensional structuresBiochemical Journal, 1994
- Cyclin is degraded by the ubiquitin pathwayNature, 1991
- Structural and functional changes associated with modification of the ubiquitin methionineBiochemistry, 1990
- Structure of polyubiquitinated histone H2ABiochemistry, 1989
- Mechanisms of Intracellular Protein BreakdownAnnual Review of Biochemistry, 1982
- Totally synthetic crystalline ribonuclease ABiopolymers, 1981
- Protein Biosynthesis: The Codon‐Specific Activation of Amino AcidsAngewandte Chemie International Edition in English, 1978
- Amino-terminal sequence identity of ubiquitin and the nonhistone component of nuclear protein A24Biochemical and Biophysical Research Communications, 1977
- Isolation of a polypeptide that has lymphocyte-differentiating properties and is probably represented universally in living cells.Proceedings of the National Academy of Sciences, 1975
- p-Alkoxybenzyl Alcohol Resin and p-Alkoxybenzyloxycarbonylhydrazide Resin for Solid Phase Synthesis of Protected Peptide FragmentsJournal of the American Chemical Society, 1973