sydneyrx2014.com Online ED Pharmacy is an 1st. pharmacy providing a personal service to the community in Australia. Over 50,000 extremely satisfied customers! We're your prescription drug store kamagra australia and have provided trusted service to families in Australia for over 15 years.

Microsoft word - exploratory ek web content.doc


Exploratory Enzyme Inhibition Analysis

Enzyme inhibition data is analyzed with the Exploratory Enzyme Kinetics option in SigmaPlot.
The direct linear plot, secondary plots and a numeric report are created to help determine if
Michaelis-Menten kinetics are satisfied and to elicit the type of inhibition. This analysis provides
excellent qualitative and quantitative information prior to fitting multiple candidate inhibition
models using the Enzyme Kinetics module.
Keywords: enzyme kinetics, inhibition, direct linear plot, secondary plots, competitive inhibition,
mixed inhibition, uncompetitive inhibition, noncompetitive inhibition.
Introduction

The Exploratory Enzyme Kinetics analysis in SigmaPlot is used to obtain qualitative and
quantitative information about the enzyme inhibition mechanism. It creates a direct linear plot,
secondary plots and a numeric report. A simple direct linear plot for six substrate and three
inhibitor concentrations is shown in Figure 1.
Figure 1. A direct linear plot showing lines defined by substrate and velocity data, intersections of those lines as black and white symbols and the medians of those intersections as alternating dark and light red symbols. The direction that the medians progress in this plot with increasing inhibitor concentration defines the type of inhibition. The Exploratory EK analysis is designed to work in conjunction with the Enzyme Kinetics module
or with data entered into a SigmaPlot worksheet.
An Exploratory EK Analysis

Enzyme inhibition data entered directly in a SigmaPlot worksheet is shown in Figure 2. There are
six groups of three replicate velocity values corresponding to the six inhibitor values in column 2.
Figure 2. An enzyme inhibition data set entered into a SigmaPlot worksheet. Two of six groups of replicate velocity values are shown. Running Exploratory Enzyme Kinetics displays the dialog The number of replicates is selected (this is not necessary if the analysis is run on an EK module worksheet) and then the type of plot is selected. For data sets like this one with relatively large number of substrate and inhibitor values, the Lines option is not selected since it clutters the graph and obscures the intersection and median information. Click Ok to run it. Two graph pages and a report are created. The graph pages are shown side-by-side in Figure 3 below. Figure 3. Two graph pages are produced by Exploratory Enzyme Kinetics. A - the direct linear and Michaelis-Menten plots. B – the two secondary plots. These plots strongly suggest mixed inhibition since the medians progress diagonally down and to the right in the direct linear plot. Also, straight lines fit the secondary plots data very well. The two inhibition constants for mixed inhibition are the intercepts of these lines with the inhibitor axis. From the upper graph Kic = 5.1 and from the lower Kiu = 12.0. The numeric report provides median values for the direct linear and secondary plots and inhibition constant estimates from the secondary plot linear regressions – Figure 4. A Partial Competitive Inhibition Example

The Michaelis-Menten plot for simulated enzyme kinetics data is shown in Figure 5A. The direct
linear plot in Figure 5B has a median trajectory that moves more-or-less horizontally from left to
right suggesting a competitive inhibition (a slight decrease in apparent Vmax can be visualized so
there is a possibility that this is mixed inhibition).
Figure 5. Michaelis-Menten (A) and direct linear plots (B) for simulated data. The secondary plots in Figure 6 give additional information. The regression line for the apparent 1/Vmax plot in Figure 6B has a slight positive slope with an inhibitor axis intercept that yields a very large inhibition constant Kiu = 1345. As seen below this is much larger than the inhibition constant Kic (=Ki) = 1.85. This slope is probably not different from zero in which case the inhibition mechanism is competitive. Figure 6. Secondary plots. The apparent Km/Vmax data in Figure 6A is fit with a hyperbolic function which intersects the inhibitor axis at -Kic = -1.85. The straight line generated does not fit the apparent Km/Vmax data well. The SigmaPlot hyperbolic function “Rational, 3 Parameter I” fit this data very well (R2 = 0.999). This suggests that the inhibition mechanism is partial since partial inhibition results in hyperbolic secondary plots (hyperbolic inhibition is another name for partial inhibition). The partial competitive inhibition parameters can be computed from the hyperbolic fit in Figure 6A
as Ki = 1.85 and α = 10.5 (we are using the Enzyme Kinetics module parameter terminology
where (Ki = Kic and αKi = Kiu). This compares well with the error-free simulation values Ki = 2.0
and α = 10.0.
A question remains as to whether the inhibition mechanism is competitive or mixed. Analysis of
the initial velocity data with all equations in the Single Substrate – Single Inhibition section of the
Enzyme Kinetics module produced the equation comparison shown in Table 1. The table is
sorted by the Akaike criterion AICc. It separates candidate equations into groups. The
competitive (partial) and mixed (partial) equations clearly form one group.
The remaining equations have AICc values nearly 100 units or more higher and therefore can be
removed from further consideration. The competitive (partial) equation has an AICc value 2 units
less than the mixed (partial) equation and, given this data set, is the best candidate. Though the
2 unit AICc difference is considered to define a difference between equations it is not a large
difference, so if determining the mechanism type is important then collecting additional data is
warranted.
Rank
Equation
Test Converg.
Table 1. Comparison of Enzyme Kinetics Module single substrate-single inhibitor equation fits to simulated data. The excellent fit of the competitive (partial) equation to this data is shown in Figure 7 by the Lineweaver-Burk plot from the Enzyme Kinetics Module. Figure 7. Lineweaver-Burk plot of the competitive (partial) equation fit to simulated data. Very good inhibition parameter estimates were obtained for the realistic 7% constant percentage error used.
Other Analyses

One can read the article: “Exploratory Enzyme Kinetics Help” for other analysis examples.

Source: http://www.systat.de/PDFs/Exploratory_Enzyme_Inhibition_Analysis.pdf

Jets_jan-april_2009.indd

Full Text Online @ www.onlinejets.org Use of antiemetics in children with acute gastroenteritis: Are they safe and effective? Henry Ford Hospital, 2799 W. Grand Blvd, Detroit, MI 48201, USA ABSTRACT The use of antiemetics is a controversial topic in treatment of pediatric gastroenteritis. Although not recommended by the American Academy of Pediatrics, antiemetics are commonly prescribed by

Engl_report12.htm

Date of the report: 07.05.2002 Report number: 12 Veterinary drugs in poultry and rabbit – secondary investigation Joint campaign by the cantons Basel Country and Basel City (main laboratory) Background Antibiotics are used in cattle, pigs and poultry to promote performance (faster growth and improved feed conversion) as well as in the prophylaxis and treatment of infectious diseases. W

Copyright © 2010-2014 Pdf Medical Search