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Isolation and characterization of alpha-macroglobulin from guinea pig plasma.

Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Research Abstract Details 

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  • Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Abstract Text:

    y suzukiY Suzuki,h sinoharaH Sinohara,

    Guinea pig alpha-macroglobulin was purified to apparent homogeneity by sequential chromatography on Sephacryl S-300, DEAE-cellulose, and hydroxyapatite. A molecular weight of 780,000 was obtained by equilibrium sedimentation. The preparation migrated as a single band of Mr = 180,000 in sodium dodecyl sulfate-polyacrylamide gel electrophoresis under reducing conditions. Rabbit antiserum raised against the final preparation partially cross-reacted with human and rat alpha-2-macroglobulins but not with rat alpha-1-macroglobulin. Guinea pig alpha-macroglobulin stimulated the amidolytic activity of trypsin towards a small substrate, but inhibited the proteolytic activity of trypsin towards remazol brilliant blue hide powder. When treated with trypsin or methylamine, four thiol groups per molecule were newly generated. The reaction with trypsin proceeded with at least at two different rates: half of the thiol groups were generated in a fast reaction and the remaining half in a slower reaction. On the other hand, such a two-step reaction was not detected in the reaction with methylamine. The methylamine-treated alpha-macroglobulin retained half the capacity to bind trypsin and its mobility in polyacrylamide gel under nondenaturing conditions remained virtually unchanged. These properties are in marked contrast to those reported for human alpha-2-macroglobulin, but resemble those of rat alpha-2- and mouse alpha-macroglobulins. The amidase activity of trypsin bound to guinea pig alpha-macroglobulin was impaired by soybean trypsin inhibitor to a much greater degree than that of trypsin bound to human or rat alpha-2-macroglobulin.

    Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Publishing Authors By Initials

    y suzukiY Suzuki,h sinoharaH Sinohara,

    For similar proteins: blood proteins: acute-phase proteins: alpha-macroglobulins research abstracts see: proteins: blood proteins: acute-phase proteins: alpha-macroglobulins research

    PUBMED ID PMID:

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    Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of biochemistry

    VOLUME: 99

    Page Numbers: 1655-65

    Journal Abbreviation: J. Biochem.

    ISSN: 0021-924X

    DAY: 19

    MONTH: Jun

    YEAR: 1986

    Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 376600

    Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Keywords Mesh Terms:

    KEYWORDS: alpha-Macroglobulins

    MESH TERMS: isolation & purification

    Chemical & Substance for Abstract: Isolation and characterization of alpha-macroglobulin from guinea pig plasma. Information

    Substance Name: Trypsin

    Registry Number: EC 3.4.21.4

    Grant and Affiliation Information for Isolation and characterization of alpha-macroglobulin from guinea pig plasma.

    AFFILIATION:

    Country: JAPAN

    JAPAN Research PublicationJAPAN Research Publication

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    MEDLINETA: J Biochem

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