Literature DB >> 2292582

Production of propeptide-directed antibody: its application to the purification of proalbumin and analysis of proalbumin processing.

K Oda1, T Fujiwara, S Ogata, Y Ikehara.   

Abstract

Antibodies which specifically recognize rat proalbumin, but not mature serum-albumin, were raised. Propeptide (NH2-Arg-Gly-Val-Phe-Arg-Arg) with an additional cysteine residue at the carboxyl terminus was conjugated to ovalbumin through either sulfide or amino group and the conjugates were injected into rabbits. Monospecific antibodies were purified on a propeptide-coupled affinity column and further immobilized as an affinity support, allowing us to purify proalbumin in a single step from rat liver microsomes. The antibodies were also used to analyze the proteolytic processing of proalbumin in primary cultured rat hepatocytes.

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Year:  1990        PMID: 2292582     DOI: 10.1093/oxfordjournals.jbchem.a123240

Source DB:  PubMed          Journal:  J Biochem        ISSN: 0021-924X            Impact factor:   3.387


  2 in total

1.  Positive charges of translocating polypeptide chain retrieve an upstream marginal hydrophobic segment from the endoplasmic reticulum lumen to the translocon.

Authors:  Hidenobu Fujita; Yuichiro Kida; Masatoshi Hagiwara; Fumiko Morimoto; Masao Sakaguchi
Journal:  Mol Biol Cell       Date:  2010-04-28       Impact factor: 4.138

2.  Conversion of secretory proteins into membrane proteins by fusing with a glycosylphosphatidylinositol anchor signal of alkaline phosphatase.

Authors:  K Oda; J Cheng; T Saku; N Takami; M Sohda; Y Misumi; Y Ikehara; J L Millán
Journal:  Biochem J       Date:  1994-07-15       Impact factor: 3.857

  2 in total

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