Plutonium is a radioactive, metallic, chemical element. It has the symbol Pu and the atomic number 94. It is the element used in most modern nuclear weapons. The most important isotope of plutonium is 239Pu, with a half-life of 24,110 years. It can be made from natural uranium and is fissile. The most stable isotope is 244Pu, with a half-life of about 80 million years, long enough to be found in extremely small quantities in nature. Nuclear materials workers sometimes call it "plute".
Notable characteristics
Plutonium is silvery in pure form, but has a yellow tarnish when oxidized.
Peculiarly, the metal goes through phases of contraction as its temperature is increased. It is also notable in that it posseses a low-symmetry structure causing it to become progressively more brittle over time.
The heat given off by alpha particle emission makes plutonium warm to the touch in reasonable quantities; larger amounts can boil water. It displays five ionic oxidation states in aqueous solution:
PuIII, as Pu3+ (blue lavender)
PuIV, as Pu4+ (yellow brown)
PuVI, as PuO22+ (pink orange)
PuV, as PuO2+ (thought to be pink; this ion is unstable in solution and will disproportionate into Pu4+ and PuO22+; the Pu4+ will then oxidize the remaining PuO2+ to PuO22+, being reduced in turn to Pu3+. Thus, aqueous solutions of plutonium tend over time towards a mixture of Pu3+ and PuO22+.)
PuVII, as PuO52- (dark red); the heptavalent ion is rare and prepared only under extreme oxidizing conditions.
Note: The color shown by Pu solutions depend on both the oxidation state and the nature of the acid anion, which influences the degree of complexing of the Pu species by the acid anion. Matlack, George: A Plutonium Primer: An Introduction to Plutonium Chemistry and its Radioactivity (LA-UR-02-6594)
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[Mini-Review] Utility of Kallikrein-Related Peptidases (KLKs) as Cancer Biomarkers Emami, N., Diamandis, E. P. Mon, 29 Sep 2008 00:00:00 -0000
Background: The human kallikrein-related peptidase (KLK) family consists of 15 highly conserved serine proteases, which are encoded by the largest uninterrupted cluster of protease genes in the human genome. To date, several members of the family have been reported as potential cancer biomarkers. Although primarily known for their biomarker value in prostate, ovarian, and breast cancers, more recent data suggest analogous roles of KLKs in several other cancers, including gastrointestinal, head and neck, lung, and brain malignancies. Among the proposed KLK cancer biomarkers, prostate-specific antigen (also known as KLK3) is the most widely recognized member in urologic oncology.
Content: Despite substantial progress in the understanding of the biomarker utility of individual KLKs, the current challenge lies in devising biomarker panels to increase the accuracy of prognosis, prediction of therapy, and diagnosis. To date, multiparametric KLK panels have been proposed for prostate, ovarian, and lung cancers. In addition to their biomarker utility, emerging evidence has revealed a number of critical functional roles for KLKs in the pathogenesis of cancer and their potential use as therapeutic targets.
Summary: KLKs have biomarker utility in many cancer types but individually lack sufficient specificity or sensitivity to be used in clinical practice; however, groups of KLKs and other candidate biomarkers may offer improved performance.
[Mini-Review] High-Abundance Polypeptides of the Human Plasma Proteome Comprising the Top 4 Logs of Polypeptide Abundance Hortin, G. L., Sviridov, D., Anderson, N. L. Mon, 29 Sep 2008 00:00:00 -0000
Background: Plasma contains thousands of proteins, but a small number of these proteins comprise the majority of protein molecules and mass.
Content: We surveyed proteomic studies to identify candidates for high-abundance polypeptide chains. We searched the literature for information on the plasma concentrations of the most abundant components in healthy adults and for the molecular mass of the mature polypeptide chains in plasma. Because proteomic studies usually dissociate proteins into polypeptide chains or detect short peptide segments of proteins, we summarized data on individual peptide chains for proteins containing multiple subunits or polypeptides. We collected data on about 150 of the most abundant polypeptides in plasma. The abundant polypeptides span approximately the top 4 logs of concentration in plasma, from 650 to 0.06 µmol/L on a molar basis or from about 50 000 to 1 mg/L mass abundance.
Conclusions: Data on the concentrations of the high-abundance peptide chains in plasma assist in understanding the composition of plasma and potential approaches for clinical laboratory or proteomic analysis of plasma proteins. Development of more extensive databases regarding the plasma concentrations of proteins in health and diseases would promote diagnostic and proteomic advances.
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