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Is promoted by higher temperatures (10). In addition to proteases, the DnaK chaperone system consisting of DnaK (Hsp70), DnaJ (Hsp40), and GrpE (nucleotide exchange factor) is required for the rapid degradation of 32 in vivo because the half-life of 32 is much longer in dnaK, dnaJ, and grpE mutants (11, 12). 32 directly interacts with DnaK or DnaJ and forms a stable ternary complex in the presenc
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, I54A 32, a very stable mutant, is more susceptible to ClpYQ and FtsH proteases than wild-type 32, indicating that the stability of 32 does not always reflect its susceptibility to proteases. Co-precipitation and gel filtration analyses show that purified 32 mutants exhibit a reduced affinity for DnaJ, leading to a marked decrease in forming a complex with DnaK in the presence of DnaJ and ATP. O
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Or color figure charges ?Immediate publication on acceptance ?Inclusion in PubMed, CAS, Scopus and Google Scholar ?Research which is freely available for redistributionSubmit your manuscript at www.biomedcentral.com/submitSeo et al. BMC Cancer 2014, 14:36 http://www.biomedcentral.com/1471-2407/14/RESEARCH ARTICLEOpen AccessPMA synergistically enhances apicularen A-induced cytotoxicity by dis
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Luble/secreted plasmid product may simultaneously gain access to the majorLuble/secreted plasmid product may simultaneously gain access to the major histocompatibility complex (MHC) class II exogenous pathway in phagocytic cells, for the [15] activation of B cells, CD4+ and CD8+ T lymphocytes . Many reports emphasized on the ability of DNA vaccines to induce immune responses against a variet
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