By Alton Meister
Advances in Enzymology and similar parts of Molecular Biology is a seminal sequence within the box of biochemistry, providing researchers entry to authoritative studies of the newest discoveries in all components of enzymology and molecular biology. those landmark volumes date again to 1941, supplying an unequalled view of the historic improvement of enzymology. The sequence deals researchers the most recent figuring out of enzymes, their mechanisms, reactions and evolution, roles in advanced organic procedure, and their software in either the laboratory and undefined. every one quantity within the sequence good points contributions through prime pioneers and investigators within the box from world wide. All articles are conscientiously edited to make sure thoroughness, caliber, and clarity.
With its wide variety of themes and lengthy old pedigree, Advances in Enzymology and similar components of Molecular Biology can be utilized not just through scholars and researchers in molecular biology, biochemistry, and enzymology, but additionally by means of any scientist drawn to the invention of an enzyme, its homes, and its applications.
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Additional resources for Advances in Enzymology and Related Areas of Molecular Biology, Volume 59
AIthough some details are not entirely consistent, it has become increasingly clear that JG22E (a hybridoma line recently. subcloned from JG22) and CSAT recognize identical antigens. A comparison of the characteristics of JG22E antigen (140-k) and CSAT antigen is given in Table VII. ” Both CSAT and JG22 monoclonal antibodies were first identified by their abilities to specifically and reversibly alter the morphology of chick myoblasts, causing them to round up and detach within 1 or 2 h (140,147).
W. Kennedy, unpublished results). These findings suggest a rather broad specificity range for the 140-k complex. CSAT antibody inhibits the initial attachment of tendon and cardiac fibroblasts and skeletal myoblasts to laminin, and also detaches these cells after they are allowed to fully attach and spread on laminin (148). The initial adhesion of skeletal myoblasts and tendon fibroblasts, but not of cardiac fibroblasts, on fibronectin substrates is also inhibited by CSAT. However all three cell types contain the 140-k complex (148).
The Kd for the 45 FIBRONECTIN 6000 I I 6000 + GRGDS 4000 2000 0 0 FRACTION NUMBER 10 20 30 Figure 7. Elution profile of purified 140-k JG22E antigen on 75 k Sepharose affinity columns. Purified 140-k was chromatographed on a 75 k-Sephdrose affinity column equilibrated with either the GRGES [O, panel (A)] or the GRGDS [0,panel ( B ) ] synthetic peptides. For reference, the elution profiles of 140-k in the presence of GRGDS in panel (A) and GRGES in panel ( B ) are indicated by the dotted lines. ( A ) In the presence of GRGES, the elution profile of the 140-k complex is asymmetrical with noticeable tailing of the peak, suggesting an interaction between the 140-k complex and the immobilized fibronectin cell-binding fragment (75 k).
Advances in Enzymology and Related Areas of Molecular Biology, Volume 59 by Alton Meister