1a8j
From Proteopedia
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| - | [[Image:1a8j.gif|left|200px]] | + | [[Image:1a8j.gif|left|200px]] |
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| - | '''IMMUNOGLOBULIN LAMBDA LIGHT CHAIN DIMER (MCG) COMPLEX WITH ASPARTAME''' | + | {{Structure |
| + | |PDB= 1a8j |SIZE=350|CAPTION= <scene name='initialview01'>1a8j</scene>, resolution 2.7Å | ||
| + | |SITE= | ||
| + | |LIGAND= <scene name='pdbligand=PME:N-L-ALPHA-ASPARTYL L-PHENYLALANINE 1-METHYL ESTER'>PME</scene> | ||
| + | |ACTIVITY= | ||
| + | |GENE= | ||
| + | }} | ||
| + | |||
| + | '''IMMUNOGLOBULIN LAMBDA LIGHT CHAIN DIMER (MCG) COMPLEX WITH ASPARTAME''' | ||
| + | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
| - | 1A8J is a [ | + | 1A8J is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1A8J OCA]. |
==Reference== | ==Reference== | ||
| - | Treatment of osteoarthritis with aspartame., Edmundson AB, Manion CV, Clin Pharmacol Ther. 1998 May;63(5):580-93. PMID:[http:// | + | Treatment of osteoarthritis with aspartame., Edmundson AB, Manion CV, Clin Pharmacol Ther. 1998 May;63(5):580-93. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9630831 9630831] |
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
[[Category: Single protein]] | [[Category: Single protein]] | ||
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[[Category: surrogate receptor]] | [[Category: surrogate receptor]] | ||
| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 09:54:27 2008'' |
Revision as of 07:54, 20 March 2008
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| Coordinates: | save as pdb, mmCIF, xml | ||||||
IMMUNOGLOBULIN LAMBDA LIGHT CHAIN DIMER (MCG) COMPLEX WITH ASPARTAME
Overview
OBJECTIVE: The binding of sweet-tasting compounds in a human (Mcg) Bence-Jones dimer has been characterized by x-ray crystallography. Aspartame binding in this immunoglobulin fragment is remarkable. Unexpected pain relief noted by A.B.E., a crystallographer with diagnosed osteoarthritis, suggested that the accommodation of aspartame in the active site of the dimer may represent surrogate binding by other proteins, with analgesia as the outcome. METHODS: X-ray analysis of the complex of aspartame and the Bence-Jones dimer was conducted with crystalline Mcg protein and pure aspartame. A single-blind (n = 1) study to confirm analgesia was completed by administration of aspartame to A.B.E. A controlled double-blind trial was performed in patients with x-ray-documented osteoarthritis. Pain and performance changes were evaluated with use of two doses of placebo and two doses of aspartame. Effects on bleeding time were then evaluated by determination of template bleeding times in 34 normal volunteers. Finally, antipyretic effects were studied in Sprague-Dawley rats given intramuscular turpentine injections. RESULTS: Aspartame binding in the Bence-Jones dimer was verified by x-ray crystallography. Improvements in performance and pain relief were observed in A.B.E. at p < 0.001. Decreased pain and improved performance were also observed in patients with osteoarthritis (p < 0.001). Mild antihemostatic responses were observed in bleeding times after aspartame treatment. Modified template bleeding times increased at p < 0.01. Aspartame blocked the turpentine-mediated febrile responses in the treated rats (p < 0.01). CONCLUSIONS: L-Aspartyl-L-phenylalanine methyl ester is biologically active and appears to relieve pain, induce mild antithrombotic effects in humans, and decrease fever in animals.
About this Structure
1A8J is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.
Reference
Treatment of osteoarthritis with aspartame., Edmundson AB, Manion CV, Clin Pharmacol Ther. 1998 May;63(5):580-93. PMID:9630831
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