1. Ryanoids and imperatoxin affect the modulation of cardiac ryanodine receptors by dihydropyridine receptor Peptide A
Maura Porta, Paula L Diaz-Sylvester, Alma Nani, Josefina Ramos-Franco, Julio A Copello Biochim Biophys Acta. 2008 Nov;1778(11):2469-79. doi: 10.1016/j.bbamem.2008.07.024. Epub 2008 Aug 3.
Ca(2+)-entry via L-type Ca(2+) channels (DHPR) is known to trigger ryanodine receptor (RyR)-mediated Ca(2+)-release from sarcoplasmic reticulum (SR). The mechanism that terminates SR Ca(2+) release is still unknown. Previous reports showed evidence of Ca(2+)-entry independent inhibition of Ca(2+) sparks by DHPR in cardiomyocytes. A peptide from the DHPR loop II-III (PepA) was reported to modulate isolated RyRs. We found that PepA induced voltage-dependent "flicker block" and transition to substates of fully-activated cardiac RyRs in planar bilayers. Substates had less voltage-dependence than block and did not represent occupancy of a ryanoid site. However, ryanoids stabilized PepA-induced events while PepA increased RyR2 affinity for ryanodol, which suggests cooperative interactions. Ryanodol stabilized Imperatoxin A (IpTx(A)) binding but when IpTx(A) bound first, it prevented ryanodol binding. Moreover, IpTx(A) and PepA excluded each other from their sites. This suggests that IpTx(A) generates a vestibular gate (either sterically or allosterically) that prevents access to the peptides and ryanodol binding sites. Inactivating gate moieties ("ball peptides") from K(+) and Na(+) channels (ShakerB and KIFMK, respectively) induced well resolved slow block and substates, which were sensitive to ryanoids and IpTx(A) and allowed, by comparison, better understanding of PepA action. The RyR2 appears to interact with PepA or ball peptides through a two-step mechanism, reminiscent of the inactivation of voltage-gated channels, which includes binding to outer (substates) and inner (block) vestibular regions in the channel conduction pathway. Our results open the possibility that "ball peptide-like" moieties in RyR2-interacting proteins could modulate SR Ca(2+) release in cells.
2. Photosensitized oxidation of methionine-containing dipeptides. From the transients to the final products
Marta T Ignasiak, Tomasz Pedzinski, Filippo Rusconi, Piotr Filipiak, Krzysztof Bobrowski, Chantal Houée-Levin, Bronislaw Marciniak J Phys Chem B. 2014 Jul 24;118(29):8549-58. doi: 10.1021/jp5039305. Epub 2014 Jul 2.
The Met residue oxidation has been studied for decades. Although many efforts have been made on the identification of free radicals, some doubts remain about their final fates, i.e., the nature of stable oxidation products. The photosensitized oxidation processes of two peptides, methionyl lysine (Met-Lys) and lysyl methionine (Lys-Met), were investigated using 3-carboxybenzophenone (3CB) as a sensitizer. Therefore, not only the transients were characterized but also the final products (by high-performance liquid chromatography and mass spectrometry) together with the quantum yields. As for the transients, the sulfur radical cations stabilized by a two-center three electron bonds with a nitrogen (S.·.N)(+) were identified in the case of Met-Lys. On the other hand, in Lys-Met, the intermolecular (S.·.S)(+) radical cations were found. The peptide-3CB adduct was the only stable product detected and was accompanied neither by sulfoxide formation nor by decarboxylation. It shows that both (S.·.N)(+) and (S.·.S)(+) radicals are converted into the relatively long-lived α-(alkylthio)alkyl radicals, which add to the 3CB-derived radicals. This addition reaction prevented all other oxidation processes such as formation of sulfoxide. The lysine residue was totally protected, which may also be of importance in biological processes.
