Abstract
We compare the physicochemical and functional characteristics of nucleoplasmin obtained from Xenopus laevis oocytes and by bacterial overexpression of a plasmid containing the nucleoplasmin gene. The comparison shows that, while the secondary structure of the protein is not affected by the method used to obtain this protein, the bacterial expressed form exhibits a marked tendency to form large aggregates and an impaired ability to displace protamines from sperm nuclei. These results add a word of caution to the indiscriminate use, in functional or structural (crystallographic) studies, of bacterially overproduced proteins that have been end-terminally tagged with polyhistidine.
Copyright 1999 Academic Press.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Amino Acid Sequence
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Animals
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Cell Nucleus / metabolism
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Chromatin / chemistry
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Chromatin / metabolism
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Circular Dichroism
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Escherichia coli / genetics
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Female
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Fishes
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Male
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Molecular Sequence Data
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Molecular Weight
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Nuclear Proteins / chemistry*
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Nuclear Proteins / genetics*
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Nuclear Proteins / metabolism
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Nucleoplasmins
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Oocytes / chemistry*
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Phosphoproteins / chemistry*
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Phosphoproteins / genetics*
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Phosphoproteins / metabolism
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Recombinant Proteins / biosynthesis*
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Recombinant Proteins / chemistry*
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Recombinant Proteins / metabolism
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Spermatozoa / metabolism
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Ultracentrifugation
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Xenopus laevis
Substances
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Chromatin
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Nuclear Proteins
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Nucleoplasmins
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Phosphoproteins
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Recombinant Proteins