Amyloid fibrils are rich in β-sheet and can be observed with thioflavin

selleckchem T (ThT) assay or by staining with Congo red, indicating that they contain a hydrophobic region. Although these fibrillar amyloids were previously considered to be the primary factor in the induction of pathology in these protein conformational diseases, recent studies indicate that small oligomers or protofibrils, rather than amyloid fibrils, may play an important role in cytotoxicity (Lesnéet al., 2006; Haataja et al., 2008). In this study, we compared TDH and TRH to investigate whether membrane toxicity by the toxins is induced by amyloidogenicity upon heating or small oligomerized tetrameric structures. TRH showed less amyloidogenicity compared with that of TDH. However, the hemolytic activity of TRH was similar to that of TDH. These data indicate that membrane disruption by the TDH family is mediated by tetrameric structures and not by the amyloidogenicity. We also compared

the circular dichroism (CD) spectra of TDH and TRH in the heat-denatured state and found that an incorrect Ivacaftor molecular weight refolding process resulted in loss of the Arrhenius effect of TRH. Purification of recombinant TDH was performed as described previously (Naim et al., 2001). N-terminal signal peptide-deleted (1–24 amino acids) trh1 (GenBank accession no. AB112353) was inserted into the expression vector pET-28a (Novagen). For the expression of recombinant TRH, we transformed a plasmid vector pET28-a harboring trh1 gene into Escherichia coli JM109 (DE3) cells (Promega). The transformant was cultured in Luria–Bertani broth (1% Bacto tryptone, 0.5% yeast extract, and 1% NaCl) containing 100 μg mL−1 of kanamycin at 30 °C for 30 h with rotary shaking, and then centrifuged at 6000 g for 30 min. We added ammonium sulfate (55% saturation) to the supernatant and allowed it to stir overnight, followed by centrifugation at 10 000 g for 1 h. The pellet was Avelestat (AZD9668) dissolved in 10 mM phosphate buffer

(pH 7.4) and dialyzed against the same buffer. We applied this solution to a series of columns: Cellulofine Hap (hydroxyapatite) (Seikagaku-Kogyo, Tokyo, Japan), Toyopearl DEAE-650M (Tosoh, Tokyo, Japan), Resource-Phe (Amersham Pharmacia Biotech AB, Uppsala, Sweden), and Superose 6 (GE Healthcare, Uppsala, Sweden). Hemolytic activities were measured as described previously (Fukui et al., 2005). Far-UV CD spectra were recorded with a J-720W spectropolarimeter (Jasco, Tokyo, Japan) equipped with a thermoelectric temperature controller. Data were analyzed with the software provided by Jasco. Measurements were taken in a quartz cuvette with a path length of 2 mm, scanned in steps of 0.2 nm at a rate of 50 nm min−1. Samples of 0.2 mg mL−1 TRH in 10 mM phosphate buffer (pH 7.4) were heated up from 37 to 90 °C at a heating rate of 0.1 °C min−1. After heat treatment at 90 °C, the temperature was decreased rapidly by 30 °C min−1 or slowly by 1 °C min−1 decrements to 37 °C.