학술논문

Purification and Characterization of Human DNA Ligase IIIα Complexes After Expression in Insect Cells
Document Type
chapter
Source
Subject
Biochemistry and Cell Biology
Biological Sciences
Biotechnology
Genetics
Underpinning research
1.1 Normal biological development and functioning
Generic health relevance
Animals
DNA Ligase ATP
DNA Ligases
DNA-Binding Proteins
Humans
Insecta
Poly-ADP-Ribose Binding Proteins
X-ray Repair Cross Complementing Protein 1
Xenopus Proteins
Affinity chromatography
Bacmid
Baculovirus
Insect cells
Ion exchange chromatography
Multiple angle light scattering
Negative stain electron microscopy
Size exclusion chromatography
Other Chemical Sciences
Developmental Biology
Biochemistry and cell biology
Medicinal and biomolecular chemistry
Language
Abstract
With improvements in biophysical approaches, there is growing interest in characterizing large, flexible multi-protein complexes. The use of recombinant baculoviruses to express heterologous genes in cultured insect cells has advantages for the expression of human protein complexes because of the ease of co-expressing multiple proteins in insect cells and the presence of a conserved post-translational machinery that introduces many of the same modifications found in human cells. Here we describe the preparation of recombinant baculoviruses expressing DNA ligase IIIα, XRCC1, and TDP1, their subsequent co-expression in cultured insect cells, the purification of complexes containing DNA ligase IIIα from insect cell lysates, and their characterization by multi-angle light scattering linked to size exclusion chromatography and negative stain electron microscopy.