Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Interactions between soluble enzymes and subcellular structure

C J Masters

    CRC Critical Reviews in Biochemistry
    |January 1, 1981
    PubMed
    Summary
    This summary is machine-generated.

    Related Concept Videos

    You might also read

    Related Articles

    Articles linked to this work by shared authors, journal, and citation graph.

    Sort by
    Same author

    On the role of the peroxisome in the metabolism of drugs and xenobiotics.

    Biochemical pharmacology·1998
    Same author

    Cellular signalling: the role of the peroxisome.

    Cellular signalling·1996
    Same author

    Chromatin structure and the expression of cardiac genes.

    Mechanisms of ageing and development·1995
    Same author

    On the role of the peroxisome in ontogeny, ageing and degenerative disease.

    Mechanisms of ageing and development·1995
    Same author

    On the ontogeny of cardiac gene transcripts.

    Mechanisms of ageing and development·1994
    Same author

    Changes in structure of the bovine milk fat globule membrane on heating whole milk.

    The Journal of dairy research·1992
    Same journal

    DNA strand exchanges.

    CRC critical reviews in biochemistry·1988
    Same journal

    Methionine biosynthesis in Enterobacteriaceae: biochemical, regulatory, and evolutionary aspects.

    CRC critical reviews in biochemistry·1988
    Same journal

    Viral RNA polymerases.

    CRC critical reviews in biochemistry·1988
    Same journal

    Positional isotope exchange.

    CRC critical reviews in biochemistry·1988
    Same journal

    Glutathione transferases--structure and catalytic activity.

    CRC critical reviews in biochemistry·1988
    Same journal

    Structure-stability relationship in proteins: fundamental tasks and strategy for the development of stabilized enzyme catalysts for biotechnology.

    CRC critical reviews in biochemistry·1988
    See all related articles

    Cellular enzyme activity is influenced by interactions with structural components, impacting metabolic regulation. New research focuses on quantifying these enzyme-structure interactions and their regulatory roles.

    Area of Science:

    • Biochemistry
    • Cell Biology
    • Metabolic Regulation

    Background:

    • Soluble enzymes are crucial for organism metabolism.
    • Enzyme activity is significantly modulated by interactions with cellular structures.
    • These interactions play a key role in metabolic regulation.

    Purpose of the Study:

    • To review the current understanding of enzyme-structure interactions in metabolic regulation.
    • To highlight advancements in experimental techniques for studying these interactions.
    • To discuss the shift towards quantitative analysis and theoretical underpinnings.

    Main Methods:

    • Review of existing literature.
    • Discussion of emerging experimental techniques.
    • Analysis of quantitative binding data and binding domain characteristics.

    Related Experiment Videos

    Main Results:

    • Experimental limitations in studying enzyme-structure interactions are being overcome.
    • Research is advancing rapidly, moving beyond basic demonstrations.
    • Focus is shifting to quantitative aspects of binding and regulatory mechanisms.

    Conclusions:

    • Enzyme-structure interactions are a critical, quantifiable aspect of metabolic regulation.
    • Advancements in techniques are enabling deeper insights into these processes.
    • Understanding these interactions is key to comprehending cellular metabolic control.