Functional Molecular Mass ofEscherichia coliK92 Polysialyltransferase As Determined by Radiation Target Analysis

Justine Vionnet; Ellis S. Kempner; Willie F. Vann

doi:10.1021/bi061486k

[24] Radiation inactivation of membrane components and molecular mass determination by target analysis

Biomembranes Part S - Methods in Enzymology ◽

10.1016/s0076-6879(89)72027-9 ◽

1989 ◽

pp. 410-439 ◽

Cited By ~ 32

Author(s):

E.S. Kempner ◽

Sidney Fleischer

Keyword(s):

Molecular Mass ◽

Mass Determination ◽

Radiation Inactivation ◽

Target Analysis ◽

Molecular Mass Determination ◽

Membrane Components

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Hydrolytic action of α-amylase on high-amylose starch of low molecular mass

Biotechnology and Applied Biochemistry ◽

10.1042/ba19990100 ◽

2000 ◽

Vol 31 (3) ◽

pp. 171 ◽

Cited By ~ 27

Author(s):

Jacob A. Rendleman, Jr.

Keyword(s):

Molecular Mass ◽

High Amylose

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A Convenient Method for Molecular Mass Determination of Heparin

Thrombosis and Haemostasis ◽

10.1055/s-0038-1646302 ◽

1992 ◽

Vol 68 (04) ◽

pp. 478-480 ◽

Cited By ~ 13

Author(s):

Jørgen Ilum Nielsen

Keyword(s):

Molecular Mass ◽

Convenient Method ◽

Mass Determination ◽

Molecular Mass Determination

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Detection of both Type 1 and Type 2 Plasminogen Activator Inhibitors in Human Monocytes

Thrombosis and Haemostasis ◽

10.1055/s-0038-1645688 ◽

1990 ◽

Vol 63 (01) ◽

pp. 067-071 ◽

Cited By ~ 10

Author(s):

Joan C Castellote ◽

Enric Grau ◽

Maria A Linde ◽

Nuria Pujol-Moix ◽

Miquel LI Rutllant

Keyword(s):

Molecular Mass ◽

Plasminogen Activator ◽

Human Peripheral Blood ◽

Direct Interaction ◽

Apparent Molecular Weight ◽

Fibrinolytic System ◽

Human Monocytes ◽

Blood Monocytes ◽

Single Chain ◽

Sds Page

SummaryIncreasing evidence suggests the involvement of leukocytes in the fibrinolytic system. Monocytes secrete pro-urokinase (Grau, Thromb Res 1989; 53: 145) and it has been shown that these cells have specific receptors for urokinase and plasminogen (Miles, Thromb Haemostas 1987; 58: 936). The aim of this study was to analyse the presence of plasminogen activator inhibitor(s) in platelet-free suspensions of human peripheral blood monocytes and polymorphonuclear leukocytes (PMN). SDS-PAGE and reverse fibrin autography showed an inhibitory band of 50 kDa in the monocyte extracts (Triton X-100) but not in the PMN extracts. Urokinase (u-PA) was mixed with increasing amounts of monocyte extract for 10 min and the mixtures were added to 125Ifibrin coated wells containing plasminogen. A dose-dependent decrease in the u-PA fibrinolytic activity was observed. The amount of inhibition increased when the monocyte releasates were preincubated with u-PA (40% inhibition after 5 min preincubation and 80% after 15 min), indicating a direct interaction between this activator and an inhibitor(s). After SDS-PAGE of monocyte extracts, immunoblotting and peroxidase staining identified both PAI1 and PAI2, with an apparent molecular weight of 47-50 kDa. Monocyte-associated PAI1 formed complexes with single chain t-PA with a molecular mass 50 kDa higher than the molecular mass of the free PAI1. However, a significant amount of PAI remained unbound to t-PA. This inactive PAI1 could have come from a rapid inactivation of the primary active PAI1. These PAI1 and PAI2 detected in human monocytes may be transcendent in the regulation of the fibrinolytic system.

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Characterization of dissolved material during the initial phase of softwood kraft pulping

TAPPI Journal ◽

10.32964/tj12.1.37 ◽

2013 ◽

Vol 12 (1) ◽

pp. 37-43 ◽

Cited By ~ 1

Author(s):

HANNU PAKKANEN ◽

TEEMU PALOHEIMO ◽

RAIMO ALÉN

Keyword(s):

Mass Transfer ◽

Molecular Mass ◽

Initial Phase ◽

Degradation Products ◽

Kraft Pulping ◽

Reaction Products ◽

Cooking Temperature ◽

Molecular Masses ◽

Aliphatic Carboxylic Acids

The influence of various cooking parameters, such as effective alkali, cooking temperature, and cooking time on the formation of high molecular mass lignin-derived and low molecular mass carbohydrates-derived (aliphatic carboxylic acids) degradation products, mainly during the initial phase of softwood kraft pulping was studied. In addition, the mass transfer of all of these degradation products was clarified based on their concentrations in the cooking liquor inside and outside of the chips. The results indicated that the degradation of the major hemicellulose component, galactoglucomannan, typically was dependent on temperature, and the maximum degradation amount was about 60%. In addition, about 60 min at 284°F (140°C) was needed for leveling off the concentrations of the characteristic reaction products (3,4-dideoxy-pentonic and glucoisosaccharinic acids) between these cooking liquors. Compared with low molecular mass aliphatic acids, the mass transfer of soluble lignin fragments with much higher molecular masses was clearly slower.

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