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1.
Biochim Biophys Acta ; 1824(12): 1366-73, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22828320

RESUMEN

Analyses of human phosphoproteome based on primary structure of the aminoacids surrounding the phosphor Ser/Thr suggest that a significant proportion of phosphosites is generated by a restricted number of acidophilic kinases, among which protein kinase CK2 plays a prominent role. Recently, new acidophilic kinases belonging to the Polo like kinase family have been characterized, with special reference to PLK1, PLK2, and PLK3 kinases. While some progress has been made in deciphering the PLK1-dependent phosphoproteome, very little is known about the targets of PLK2 and PLK3 kinases. In this report by using an in vitro approach, consisting of cell lysate phosphorylation, phosphoprotein separation by 2D gel electrophoresis and mass spectrometry, we describe the identification of new potential substrates of PLK2 and PLK3 kinases. We have identified and validated as in vitro PLK2 and PLK3 substrates HSP90, GRP-94, ß-tubulin, calumenin, and 14-3-3 epsilon. The phosphosites generated by PLK3 in these proteins have been identified by mass spectrometry analysis to get new insights about PLKs specificity determinants. These latter have been further corroborated by an in silico analysis of the PLKs substrate binding region.


Asunto(s)
Proteínas Serina-Treonina Quinasas/metabolismo , Secuencia de Aminoácidos , Células Cultivadas , Humanos , Espectrometría de Masas , Modelos Moleculares , Datos de Secuencia Molecular , Fosforilación , Dominios y Motivos de Interacción de Proteínas , Homología Estructural de Proteína , Especificidad por Sustrato , Proteínas Supresoras de Tumor
2.
Curr Top Med Chem ; 11(11): 1340-51, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21513497

RESUMEN

CK2 denotes a pleiotropic, constitutively active protein kinase whose abnormally high level in many cancer cells is held as an example of "non oncogene addiction". A wide spectrum of cell permeable, fairly specific ATP site-directed CK2 inhibitors are currently available which are proving useful to dissect its biological functions and which share the property of inducing apoptosis of cancer cells with no comparable effect on their "normal" counterparts. One of these, CX-4945, has recently entered clinical trials for the treatment of advanced solid tumors, Castelman's disease and multiple myeloma. The solution of a wide range of 3D structures of inhibitors bound to the catalytic subunits of CK2 reveals that their efficacy substantially relies on hydrophobic interactions within a cavity which is smaller than in other protein kinases. Accordingly the potency of tetra-halogenated benzimidazoles increases upon replacement of chlorine by bromine and, even more, by iodine, and decreases if two unique bulky side chains on CK2 (Val66 and Ile174) are mutated to alanines. Many CK2 inhibitors have been tested on a panel of more than 60 kinases providing Promiscuity Scores useful to evaluate their selectivity, the lowest value (9.47), denoting highest selectivity, being displayed by quinalizarin. The observation that CK2 inhibitors with medium/high promiscuity scores share the ability to inhibit a group of protein kinases as effectively as CK2 discloses the possibility of using their scaffolds for the rational development of selective inhibitors of these kinases, with special reference to PIMs, DYRKs, HIPK2, PKD and ERK8.


Asunto(s)
Adenosina Trifosfato/metabolismo , Antineoplásicos/farmacología , Quinasa de la Caseína II/antagonistas & inhibidores , Neoplasias/tratamiento farmacológico , Inhibidores de Proteínas Quinasas/farmacología , Antineoplásicos/síntesis química , Antineoplásicos/química , Quinasa de la Caseína II/química , Quinasa de la Caseína II/metabolismo , Humanos , Neoplasias/enzimología , Neoplasias/metabolismo , Inhibidores de Proteínas Quinasas/síntesis química , Inhibidores de Proteínas Quinasas/química , Relación Estructura-Actividad
3.
Environ Pollut ; 157(7): 2108-17, 2009 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-19285369

RESUMEN

Three ex situ collections of poplar clones from natural populations of Populus alba and P. nigra growing in northern Italy were assessed for their genetic dissimilarity (GD) by means of amplified fragment length polymorphism (AFLP). The high GD evidenced within populations was exploited for screening 168 clones in a field trial on heavy metal-polluted soil. After one growth season, clonal differences in plant survival and growth were observed. On the basis of performance, six clones were singled out, and used to evaluate copper and zinc accumulation in different organs. Clonal differences in metal concentrations were most evident for leaves and stems; one clone of P. alba (AL35) had a distinctly higher concentration of both metals in the roots. Leaf polyamine (putrescine, spermidine, spermine) profiles correlated with tissue metal concentrations, depending on the clone, plant organ and metal. In particular, the high metal-accumulating clone AL35 exhibited a dramatically higher concentration of free and conjugated putrescine. Overall, the results indicate that, given the high GD of Populus even within populations, it is possible to identify genotypes best suited for soil clean-up, and useful also for investigating physiological markers associated with high metal accumulation/tolerance.


Asunto(s)
Células Clonales , Metales Pesados/toxicidad , Hojas de la Planta/química , Poliaminas/análisis , Populus/genética , Contaminantes del Suelo/toxicidad , Cobre/análisis , Cobre/toxicidad , Ecología/métodos , Italia , Metales Pesados/análisis , Hojas de la Planta/efectos de los fármacos , Raíces de Plantas/química , Tallos de la Planta/química , Populus/efectos de los fármacos , Populus/crecimiento & desarrollo , Suelo/análisis , Contaminantes del Suelo/análisis , Zinc/análisis , Zinc/toxicidad
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