DNA CHIP
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Friday, March 12, 2010
Thursday, March 11, 2010
Find a protein using PDB explorer, describe you protein including disease state or real world application it has.
* Find a protein using PDB explorer, describe you protein including disease state or real world application it has.
When looking to perform research on proteins, one finds that there are many entry level sites available for free on the web. I have linked a couple of the sites below. I have chosen to find and report HIV protease. This is a key enzyme contributing to the overall virulence factor of HIV/AIDS. I recently, March 4th do be exact presented a PowerPoint presentation. The presentation happened to be on targeting proteins, more specifically enzymes in the treatment of HIV. I have placed a link to the presentation below. I hope that this presentation can answer the question of how a protein can related to a disease and more importantly, how can targeting that proteins function impact the virulence of the disease.
Specifically, when the new virus buds off from the host cell, it achieves maturation
by HIV protease cleaving the longs budding strands into fragments of smaller size. These smaller fragments are the functional strands which are packaged into other viral components in order to create a new virus.
into smaller functional fragments by HIV proteases
PowerPoint presentation on HIV/AIDS, March 4th, 2010.
HIV/AIDS ENZYME TREATMENT
Protein Database Site:
MCSG Goverment Site
Additional Protein Site:
www.RCSB.org
___________________________________________________________
Protein of interest:
HIV Protease (Quaternary Structure)
HIV Protease
_______________________________________
Protease inhibitors (PIs) are a class of drugs used to treat or prevent infection by viruses, including HIV and Hepatitis C. PIs prevent viral replication by inhibiting the activity of HIV-1 protease, an enzyme used by the viruses to cleave nascent proteins for final assembly of new virons.
Protease inhibitors have been developed or are presently undergoing testing for treating various viruses:
About Wikepedia and Pasting:
________________________________________________________
When you paste from Wikipedia, please note that the information can be just plain wrong. But it contains some much information that is both accessible and easy to use. When you paste a paragraph, often the links paste with it, giving you the links back to the site. This is self serving and can be a distraction to your site, due to the fact that you navigate away from your site, but it can be a great way of presenting NON-FACT CHECKED INFORMATION easily and without a ton of effort on your part.
ENJOY READING THE REMAINDER OF THE BLOG ENTRIES BELOW.
MCB
Signing Off :-)
___________________________________________________________
When looking to perform research on proteins, one finds that there are many entry level sites available for free on the web. I have linked a couple of the sites below. I have chosen to find and report HIV protease. This is a key enzyme contributing to the overall virulence factor of HIV/AIDS. I recently, March 4th do be exact presented a PowerPoint presentation. The presentation happened to be on targeting proteins, more specifically enzymes in the treatment of HIV. I have placed a link to the presentation below. I hope that this presentation can answer the question of how a protein can related to a disease and more importantly, how can targeting that proteins function impact the virulence of the disease.
Specifically, when the new virus buds off from the host cell, it achieves maturation
by HIV protease cleaving the longs budding strands into fragments of smaller size. These smaller fragments are the functional strands which are packaged into other viral components in order to create a new virus.
into smaller functional fragments by HIV proteases
PowerPoint presentation on HIV/AIDS, March 4th, 2010.
HIV/AIDS ENZYME TREATMENT
Protein Database Site:
MCSG Goverment Site
Additional Protein Site:
www.RCSB.org
___________________________________________________________
Protein of interest:
HIV Protease (Quaternary Structure)
HIV Protease
HIV Protease from the RCSB site pasted below:
Fragment-Based Screen against HIV Protease
Perryman, A.P., Zhang, Q., Soutter, H.H., Rosenfeld, R., McRee, D.E., Olson, A.J., Elder, J.E., Stout, C.D.
(2010) Chem.Biol.Drug Des. 75: 257-268
Perryman, A.P., Zhang, Q., Soutter, H.H., Rosenfeld, R., McRee, D.E., Olson, A.J., Elder, J.E., Stout, C.D.
(2010) Chem.Biol.Drug Des. 75: 257-268
Source
Hide Polymer: 1 Scientific Name: Human immunodeficiency virus 1 Expression System: Escherichia coli
Hide Id Details 2AZ8 HIV-1 PROTEASE NL4-3 IN COMPLEX WITH INHIBITOR, TL-3, WILD TYPE 2AZ9 HIV-1 PROTEASE NL4-3 IN COMPLEX WITH INHIBITOR, TL-3, 1X MUTANT 2AZB HIV-1 PROTEASE NL4-3 IN COMPLEX WITH INHIBITOR, TL-3, 3X MUTANT 2AZC HIV-1 PROTEASE NL4-3 IN COMPLEX WITH INHIBITOR, TL-3, 6X MUTANT 3KF1 HIV Protease (PR) dimer without inhibitor; acetate in exo site 3KFN HIV Protease (PR) with inhibitor TL-3 and fragment hit 4D9 by soaking 3KFP HIV Protease (PR) with inhibitor TL-3 bound, and DMSOs in exo site 3KFR HIV Protease (PR) dimer with inhibitor TL-3 bound and fragment 1F1 in the outside/top of flap 3KFS HIV Protease (PR) dimer with inhibitor TL-3 bound and fragment 2F4 in the outside/top of flap
The above information is a sample of the type of information one can find while visiting a a protein database site. The information can be kind of overwhelming, but this is the nature of current molecular research today. It will probably only get more detailed from here, in the future.
______________________________________________
General Information about Protease inhibitors Pasted Below from Wikipedia:
Protease inhibitor (pharmacology)
From Wikipedia, the free encyclopedia:
Protease inhibitors (PIs) are a class of drugs used to treat or prevent infection by viruses, including HIV and Hepatitis C. PIs prevent viral replication by inhibiting the activity of HIV-1 protease, an enzyme used by the viruses to cleave nascent proteins for final assembly of new virons.
Protease inhibitors have been developed or are presently undergoing testing for treating various viruses:
- HIV/AIDS: antiretroviral protease inhibitors (saquinavir, ritonavir, indinavir, nelfinavir, amprenavir[1] etc.)
- Hepatitis C: experimental agents: BILN 2061 (All clinical trials of BILN 2061 have been suspended due to cardiac issues), VX 950 (trade name Telaprevir), or SCH 503034[2]
About Wikepedia and Pasting:
________________________________________________________
When you paste from Wikipedia, please note that the information can be just plain wrong. But it contains some much information that is both accessible and easy to use. When you paste a paragraph, often the links paste with it, giving you the links back to the site. This is self serving and can be a distraction to your site, due to the fact that you navigate away from your site, but it can be a great way of presenting NON-FACT CHECKED INFORMATION easily and without a ton of effort on your part.
ENJOY READING THE REMAINDER OF THE BLOG ENTRIES BELOW.
MCB
Signing Off :-)
___________________________________________________________
Friday, March 5, 2010
Responce to the Questions asked by class mates about March 4th, 2010, Pesentation on: Treatment fo AIDS by Enzymatic Targets.
On March 4th I gave a 5 minute presentation on: The Treatment of AIDS. The class was kind enough to post some questions after the presentation was finished. I have looked up possible answers to the questions asked.
PLEASE NOTE THAT THE PowerPoint IS LINKED ABOVE IN PROTEIN BLOG.
The following passages are written in response to the questions asked and my results found pertaining to them:
Please note: I am no authority on this subject and if anybody has another view, please post a comment to the blog. I wish for this blog not only to be accurate, but to be representative of a variety of viewpoints.
* HIV is the beginning and AIDS is actively replicating disease phase?
Yes, I reversed these two distinctions during the presentation.
* Are the cells called CD 4 or is that another aspect?
That is another aspect, they are commonly referred to as CD 4, but that is an antigen they carry, not the cell itself the immune cell commonly called the Helper T cell would be more accurate.
"It turns out that CD4 isn't enough. Another protein called CCR5 is needed as well. CCR5, called a co-receptor because it works with CD4, is the door that opens to allow HIV to enter the cell." Stanford School of Medicine Blog:
http://www.thetech.org/genetics/news.php?id=13
* Is AIDS transmitted to Offspring Via the mother?
AIDS can cross the placental barrier, but not always.
AIDS does not appear to be readily passed to offspring genetically.
"If a pro-virus has been integrated into germ-line cells (eggs or sperm), it is passed on to the following generation (the offspring). This process has been occurring for many thousands of years in humans and these retro-viral sequences now account for approximately 8% of the human genome!"
http://www.biotrends.org/science_society/science_society_Science_Basics_HIVAIDS.htm
Targeted Cells:
The virus, entering through which various routes, act primarily on the following cells:
* Lymphoreticular system:
o CD4+ T-Helper cells
o Macrophages
o Monocytes
o B-lymphocytes
* Certain endothelial cells
* Central nervous system:
o Microglia of the nervous system
o Astrocytes
o Oligodendrocytes
o Neurones – indirectly by the action of cytokines and the gp-120
Source: The Wikipedia site had the above list of affected somatic cells.
Note: the gametic cells, responsible for sexual reproduction are not on the list.
* What are the treatments for AIDS?
HAART, or Highly Active Anti-retro viral Therapy is a cocktail taken multiple times per day by aids patients. This is the new front line medication for HIV/AIDS. This chemotherapy can halt the progression of the disease dramatically.
http://www.healthscout.com/ency/68/101/main.html
* Had I heard of a patient who is clear of HIV for 2 years post bone marrow transplant?
Yes, I believe that I had heard of a person in Germany who was immune and they did a graft to try and get the immune cells to multiply.
Wikipedia had this to say about the German patient:
"In Berlin, Germany, a 42-year-old leukemia patient infected with HIV for more than a decade was given an experimental transplant of bone marrow with cells that contained an unusual natural variant of the CCR5 cell-surface receptor. This CCR5-Δ32 variant has been shown to make some cells from people who are born with it resistant to infection with some strains of HIV. Almost two years after the transplant, and even after the patient reportedly stopped taking anti-retro viral medications, HIV has not been detected in the patient's blood.[126]"
Thanks again to my fellow students for your questions and especially for your corrections.
I look forward to the rest of the presentations!!!
MCB
PLEASE NOTE THAT THE PowerPoint IS LINKED ABOVE IN PROTEIN BLOG.
The following passages are written in response to the questions asked and my results found pertaining to them:
Please note: I am no authority on this subject and if anybody has another view, please post a comment to the blog. I wish for this blog not only to be accurate, but to be representative of a variety of viewpoints.
* HIV is the beginning and AIDS is actively replicating disease phase?
Yes, I reversed these two distinctions during the presentation.
* Are the cells called CD 4 or is that another aspect?
That is another aspect, they are commonly referred to as CD 4, but that is an antigen they carry, not the cell itself the immune cell commonly called the Helper T cell would be more accurate.
"It turns out that CD4 isn't enough. Another protein called CCR5 is needed as well. CCR5, called a co-receptor because it works with CD4, is the door that opens to allow HIV to enter the cell." Stanford School of Medicine Blog:
http://www.thetech.org/genetics/news.php?id=13
* Is AIDS transmitted to Offspring Via the mother?
AIDS can cross the placental barrier, but not always.
AIDS does not appear to be readily passed to offspring genetically.
"If a pro-virus has been integrated into germ-line cells (eggs or sperm), it is passed on to the following generation (the offspring). This process has been occurring for many thousands of years in humans and these retro-viral sequences now account for approximately 8% of the human genome!"
http://www.biotrends.org/science_society/science_society_Science_Basics_HIVAIDS.htm
Targeted Cells:
The virus, entering through which various routes, act primarily on the following cells:
* Lymphoreticular system:
o CD4+ T-Helper cells
o Macrophages
o Monocytes
o B-lymphocytes
* Certain endothelial cells
* Central nervous system:
o Microglia of the nervous system
o Astrocytes
o Oligodendrocytes
o Neurones – indirectly by the action of cytokines and the gp-120
Source: The Wikipedia site had the above list of affected somatic cells.
Note: the gametic cells, responsible for sexual reproduction are not on the list.
* What are the treatments for AIDS?
HAART, or Highly Active Anti-retro viral Therapy is a cocktail taken multiple times per day by aids patients. This is the new front line medication for HIV/AIDS. This chemotherapy can halt the progression of the disease dramatically.
http://www.healthscout.com/ency/68/101/main.html
* Had I heard of a patient who is clear of HIV for 2 years post bone marrow transplant?
Yes, I believe that I had heard of a person in Germany who was immune and they did a graft to try and get the immune cells to multiply.
Wikipedia had this to say about the German patient:
"In Berlin, Germany, a 42-year-old leukemia patient infected with HIV for more than a decade was given an experimental transplant of bone marrow with cells that contained an unusual natural variant of the CCR5 cell-surface receptor. This CCR5-Δ32 variant has been shown to make some cells from people who are born with it resistant to infection with some strains of HIV. Almost two years after the transplant, and even after the patient reportedly stopped taking anti-retro viral medications, HIV has not been detected in the patient's blood.[126]"
Thanks again to my fellow students for your questions and especially for your corrections.
I look forward to the rest of the presentations!!!
MCB
Monday, February 15, 2010
Reflection
While having reflecting on three major topics studied during the semester in biochemistry and how they connect with the classroom discussion, I prepare to enter my semester end blog.
The question: How would you connect with the topics today, i.e. what did you know before the course? What have you learned about these three topics during the course?
The topics:
The steroid group
Sex hormones
The sodium/potassium pump
While discussing these three topics of interest, I will be leaning heavily upon the class text Biochemistry, by Campbell, Farrell & Shawn and PowerPoint class notes.
My knowledge for all three topics discussed below was on a very basic level. The knowledge of both structure and function was above my level of knowledge at the start of class in late January.
The first topic that I wish to discuss is the steroid group cholesterol, perhaps the most common, but least recognized as a steroid. Cholesterol is a critical steroid when it comes to the proper function of the human body. The primary structure is uniform, comprised of three (6) membered rings and a single (5) membered ring, followed by a carbon chain of varying lengths. Cholesterol serves as an important steroid, critical to the structural integrity of our cells. Cholesterols also serve as precursors to many other important biomolecules. Embedded in the Phospolipid bilayer, cholesterol add to the cell membranes rigidity and help to form bonds that firm up these basic but important cell wall structures and ultimately serve to give the body strength through a well-connected muscular undercarriage. Finally, it is important to mention that there are two forms of cholesterol HDL and LDL. HDL is high density, the “good” and LDL is low density or the “Bad” form.
Google to Blog Spot for a page on Cell wall: apbio82007.blogspot.com/.../cell-membrane.html
The sex hormones are arguably the next most common steroid group besides cholesterol, due to the important effects that they mediate and the fact that they are cholesterol derivatives and without regular intake of cholesterol from our diet, our bodies would have to expend drastic amounts of energy modifying other precursor molecules into essential hormones. They include, but are not limited to testosterone, estrogen and progesterone. These steroids are critical to normal function of primary sexual function as well as other various types of processes. These steroids follow the ring structure model listed above for cholesterol, the 6:6:6:5 ring fusion conformation, giving them steroid status, but have undergone various chain modifications to make them into specific sex hormones.
The second area of interest is the biomolecule the triacylglycerol group. These molecules are composed of three fatty acids and one glycerol molecule joined by three separate dehydration reactions, which forms an ester linkages between the fatty acids and the glycerol. These molecules are found in adipose tissue and carry a 2:1 ration for energy, when comparing a molecule of triacylglycerol to a carbohydrate or protein. These molecules are truly the fuel of humanity.
The third and final topic of reflection is the Potassium/Sodium pump. Specifically, the action of the three sodium molecules brought out of the typical human cell, the two Potassium molecules brought into the typical human cell, and the action potential given by one ATP or specifically one Phosphate atom’s bond energy to drive the reaction. Note: if the process is reversed, in response to a change in the direction of the gradient, although more rare, ATP is produced as a result. This is an example of a membrane protein within a cell changing conformation, in a number of different ways, at a number of different sites, to result in the correct substrates attaching to the correct areas and the complicated function of ion transport.
My take-away point for this semester is the newfound understanding of complexity when it comes to biomolecules and their roles in the workings of the human body. It may appear simple when looking at just one topic on its own, but as I have learned this semester, the synthesis of any number of systems with one another, describes a system of almost infinite complexity.
In all three cases, I have possessed a reasonably functional knowledge of the subject matter. The advantage of taking Biochemistry has been to tie in the working knowledge between these separate topics and thus advancing ones knowledge of the topics individually and collectively.
Thanks, Biochem you’re the best.
MCB
The question: How would you connect with the topics today, i.e. what did you know before the course? What have you learned about these three topics during the course?
The topics:
The steroid group
Sex hormones
The sodium/potassium pump
While discussing these three topics of interest, I will be leaning heavily upon the class text Biochemistry, by Campbell, Farrell & Shawn and PowerPoint class notes.
My knowledge for all three topics discussed below was on a very basic level. The knowledge of both structure and function was above my level of knowledge at the start of class in late January.
The first topic that I wish to discuss is the steroid group cholesterol, perhaps the most common, but least recognized as a steroid. Cholesterol is a critical steroid when it comes to the proper function of the human body. The primary structure is uniform, comprised of three (6) membered rings and a single (5) membered ring, followed by a carbon chain of varying lengths. Cholesterol serves as an important steroid, critical to the structural integrity of our cells. Cholesterols also serve as precursors to many other important biomolecules. Embedded in the Phospolipid bilayer, cholesterol add to the cell membranes rigidity and help to form bonds that firm up these basic but important cell wall structures and ultimately serve to give the body strength through a well-connected muscular undercarriage. Finally, it is important to mention that there are two forms of cholesterol HDL and LDL. HDL is high density, the “good” and LDL is low density or the “Bad” form.
Google to Blog Spot for a page on Cell wall: apbio82007.blogspot.com/.../cell-membrane.html
The sex hormones are arguably the next most common steroid group besides cholesterol, due to the important effects that they mediate and the fact that they are cholesterol derivatives and without regular intake of cholesterol from our diet, our bodies would have to expend drastic amounts of energy modifying other precursor molecules into essential hormones. They include, but are not limited to testosterone, estrogen and progesterone. These steroids are critical to normal function of primary sexual function as well as other various types of processes. These steroids follow the ring structure model listed above for cholesterol, the 6:6:6:5 ring fusion conformation, giving them steroid status, but have undergone various chain modifications to make them into specific sex hormones.
The second area of interest is the biomolecule the triacylglycerol group. These molecules are composed of three fatty acids and one glycerol molecule joined by three separate dehydration reactions, which forms an ester linkages between the fatty acids and the glycerol. These molecules are found in adipose tissue and carry a 2:1 ration for energy, when comparing a molecule of triacylglycerol to a carbohydrate or protein. These molecules are truly the fuel of humanity.
The third and final topic of reflection is the Potassium/Sodium pump. Specifically, the action of the three sodium molecules brought out of the typical human cell, the two Potassium molecules brought into the typical human cell, and the action potential given by one ATP or specifically one Phosphate atom’s bond energy to drive the reaction. Note: if the process is reversed, in response to a change in the direction of the gradient, although more rare, ATP is produced as a result. This is an example of a membrane protein within a cell changing conformation, in a number of different ways, at a number of different sites, to result in the correct substrates attaching to the correct areas and the complicated function of ion transport.
My take-away point for this semester is the newfound understanding of complexity when it comes to biomolecules and their roles in the workings of the human body. It may appear simple when looking at just one topic on its own, but as I have learned this semester, the synthesis of any number of systems with one another, describes a system of almost infinite complexity.
In all three cases, I have possessed a reasonably functional knowledge of the subject matter. The advantage of taking Biochemistry has been to tie in the working knowledge between these separate topics and thus advancing ones knowledge of the topics individually and collectively.
Thanks, Biochem you’re the best.
MCB
Energy Metabolism
How would you explain to a friend, energy metabolism, (i.e. glucose entering the body and energy creation} using your knowledge from Biochemistry?
Well I am not so sure that my friends would appreciate having me tell them about energy intake and metabolism, but here it goes.
We take in complex forms of food in order to survive. It is the bodies job to break them down and metabolize the less complex more fully catabolized products to make and store energy from intermediates. The sugar glucose and its stored form glycogen are the primary intermediates used in energy metabolism in the human body. Without glucose we last about 4 minutes before our bodies start to shut down. Within a half hour, our bodily extreme short-term stores would be tapped and we would be dead. The key word is stores. The body stores energy for normal fasting and times of famine in the form of fat and muscle in the case of extreme famine. It would be likely that we would just run out of glucose like we might run out of air when we stop breathing, but extreme athletes must not only keep up their critical electrolyte balance, but also their blood glucose levels. Diabetics deal with swings in glucose levels on a daily basis, due to the lack of regular or functional insulin production. This condition can absolutely be fatal when the sugar unbalance swings to far in either direction. The body has evolved under the condition known as homeostasis, meaning that the body self regulates to stay in working balance. The sugar balance regulation in our blood is no exception.
In addition to the glucose in blood, glucose leaving the blood and entering each cell in our bodies is as, if not more important than any other form. The cells in the body utilize the symbiont organelle the mitochondria to produce our energy currency AMP, ADP, and ATP. These molecules are our source of life. The energy stored in advance in the bonds of these and a select group of other molecules power all of the chemical reactions in our bodies, every second of the day.
Well this was the basic knowledge that I have learned about glucose metabolism and the subsequent ATP production once glucose has entered our bodies.
MCB
Well I am not so sure that my friends would appreciate having me tell them about energy intake and metabolism, but here it goes.
We take in complex forms of food in order to survive. It is the bodies job to break them down and metabolize the less complex more fully catabolized products to make and store energy from intermediates. The sugar glucose and its stored form glycogen are the primary intermediates used in energy metabolism in the human body. Without glucose we last about 4 minutes before our bodies start to shut down. Within a half hour, our bodily extreme short-term stores would be tapped and we would be dead. The key word is stores. The body stores energy for normal fasting and times of famine in the form of fat and muscle in the case of extreme famine. It would be likely that we would just run out of glucose like we might run out of air when we stop breathing, but extreme athletes must not only keep up their critical electrolyte balance, but also their blood glucose levels. Diabetics deal with swings in glucose levels on a daily basis, due to the lack of regular or functional insulin production. This condition can absolutely be fatal when the sugar unbalance swings to far in either direction. The body has evolved under the condition known as homeostasis, meaning that the body self regulates to stay in working balance. The sugar balance regulation in our blood is no exception.
In addition to the glucose in blood, glucose leaving the blood and entering each cell in our bodies is as, if not more important than any other form. The cells in the body utilize the symbiont organelle the mitochondria to produce our energy currency AMP, ADP, and ATP. These molecules are our source of life. The energy stored in advance in the bonds of these and a select group of other molecules power all of the chemical reactions in our bodies, every second of the day.
Well this was the basic knowledge that I have learned about glucose metabolism and the subsequent ATP production once glucose has entered our bodies.
MCB
Again, Knowledge
What knowledge have you connected with past knowledge during Biochemistry?
Using the text, Campbell & Farrell, Biochemistry and classroom PowerPoint presentations, I wish to confer my new and improved understanding of enzymes and their specific characteristics. First and most importantly, is the fact that their are two main groups of enzymes, differentiated by the form of activation. The naming of both groups follows a the same pattern. That is the descriptive of what it pertains or acts on and the suffix "-ase". Lipase is active on lipids and is a typical naming example.
The first and probably the more simple of the two is the non-allosteric enzyme. This form of enzyme is either activated or inhibited by a non-competitive inhibitor through the active site or main physical shape specific connection to other molecules; most often taking the shape of proteins. This category of enzymes follow a very specific and well defined mathematical model called the Michaelis Menton model, the equations and specifics of which are readily available on line. This model when graphed produces a hyperbolic curve, making it easy to pick out when all that you have to go by is a graph on a exam or lab practical.
The second and probably more complex of the two is the allosteric enzyme. The allosteric enzyme is so named, for its additional "allosteric" activation site. Instead of following the Michaelis Menton model for behavior, the allosteric enzyme group instead follows the "sequential model". Hemoglobin is a terrific and familiar example of this model, exhibiting this type of binding type of binding. In the case of Oxygen binding on the individual heme subunits, the binding affinity increases with 1 to 4 Oxygen atoms bound. This transforms the enzyme from a type T to a Type T-R, to a Type R as the atomic unit substrates bind to the quaternary subunits.
Finally and possibly more important is the action of the enzymes no matter the type. Enzymes are catalysts first and foremost. All catalysts, however, are not created equal. The enzymatic catalytic reactions are several orders of magnitude better than the best non-enzymatic catalyst reaction. This means that the reaction in living organisms can be fast enough and efficient enough to maintain the various complex systems of life. In short, we owe much of who and what we are to enzymes.
MCB
Using the text, Campbell & Farrell, Biochemistry and classroom PowerPoint presentations, I wish to confer my new and improved understanding of enzymes and their specific characteristics. First and most importantly, is the fact that their are two main groups of enzymes, differentiated by the form of activation. The naming of both groups follows a the same pattern. That is the descriptive of what it pertains or acts on and the suffix "-ase". Lipase is active on lipids and is a typical naming example.
The first and probably the more simple of the two is the non-allosteric enzyme. This form of enzyme is either activated or inhibited by a non-competitive inhibitor through the active site or main physical shape specific connection to other molecules; most often taking the shape of proteins. This category of enzymes follow a very specific and well defined mathematical model called the Michaelis Menton model, the equations and specifics of which are readily available on line. This model when graphed produces a hyperbolic curve, making it easy to pick out when all that you have to go by is a graph on a exam or lab practical.
The second and probably more complex of the two is the allosteric enzyme. The allosteric enzyme is so named, for its additional "allosteric" activation site. Instead of following the Michaelis Menton model for behavior, the allosteric enzyme group instead follows the "sequential model". Hemoglobin is a terrific and familiar example of this model, exhibiting this type of binding type of binding. In the case of Oxygen binding on the individual heme subunits, the binding affinity increases with 1 to 4 Oxygen atoms bound. This transforms the enzyme from a type T to a Type T-R, to a Type R as the atomic unit substrates bind to the quaternary subunits.
Finally and possibly more important is the action of the enzymes no matter the type. Enzymes are catalysts first and foremost. All catalysts, however, are not created equal. The enzymatic catalytic reactions are several orders of magnitude better than the best non-enzymatic catalyst reaction. This means that the reaction in living organisms can be fast enough and efficient enough to maintain the various complex systems of life. In short, we owe much of who and what we are to enzymes.
MCB
Biochemistry Web Site
Find an interesting Biochemistry web site. Describe and place link to site in blog.
Site: http://www.medicalnewstoday.com/sections/biology-biochemistry/
The above website is a great resource for not only doing research, but also just reading about: Medical topics, Prosthetic Device topics, Biochemical topic, biology topics and much more. The site is almost as diverse as biochemistry itself. I enjoy the variety of articles listed. Whether you are from a medical, research, industrial high-tech or other background, there is something for just about everyone.
The following are the new topics/full articles from today, March 8th, 2010 as listed on the site:
* Ritalin Boosts Learning By Increasing Brain Plasticity
* In Stanford, Mathematical Innovation Turns Blood Draw Into Information Gold Mine
* New Sensor Array Detects Single Molecules For The First Time
* Experimental Vaccine Protects Monkeys Against Chikungunya
* Evolutionary Biologist: Studies The Co-Evolution Of Humans And Diseases
Diverse as biochemistry itself right? Well maybe not, but there is potentially something for everyone. The health video section is a powerful learning tool for those in the medical profession, the public and of course students. Possibly best of all is that the site is free to the public and constantly changing and updating from day to day.
MCB
Site: http://www.medicalnewstoday.com/sections/biology-biochemistry/
The above website is a great resource for not only doing research, but also just reading about: Medical topics, Prosthetic Device topics, Biochemical topic, biology topics and much more. The site is almost as diverse as biochemistry itself. I enjoy the variety of articles listed. Whether you are from a medical, research, industrial high-tech or other background, there is something for just about everyone.
The following are the new topics/full articles from today, March 8th, 2010 as listed on the site:
* Ritalin Boosts Learning By Increasing Brain Plasticity
* In Stanford, Mathematical Innovation Turns Blood Draw Into Information Gold Mine
* New Sensor Array Detects Single Molecules For The First Time
* Experimental Vaccine Protects Monkeys Against Chikungunya
* Evolutionary Biologist: Studies The Co-Evolution Of Humans And Diseases
Diverse as biochemistry itself right? Well maybe not, but there is potentially something for everyone. The health video section is a powerful learning tool for those in the medical profession, the public and of course students. Possibly best of all is that the site is free to the public and constantly changing and updating from day to day.
MCB
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