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1.
The recent crystallization and structural analysis of the ATP(ADP)-complex of the N-terminal domain of the 90 kDa heat shock
protein (Hsp90) confirmed our earlier findings on the ATP-binding properties of Hsp90. Here we further characterize the nucleotide
binding of Hsp90 by demonstrating that surface plasmon resonance measurements also indicate a low-affinity binding of ATP
to Hsp90 and that [α-32P]ATP seems to have an equal preference for monomers, dimers and oligomers of Hsp90 on native polyacrylamide gels. Finally
we discuss some of our results which raise the possibility that Hsp90 has two nucleotide binding sites (one in its N-terminal
and another in the C-terminal domain) and that the nucleotide binding to Hsp90 dimers may display a positive cooperativity
under some special conditions. The submillimolar binding affinity of ATP to Hsp90 allows the regulation of some Hsp90-related
functions just in the range of ATP-level fluctuations during stress or during the cell cycle. 相似文献
2.
《Bioorganic & medicinal chemistry》2019,27(21):115080
Cells constantly need to adopt to changing environmental conditions, maintaining homeostasis and proteostasis. Heat shock proteins are a diverse class of molecular chaperones that assist proteins in folding to prevent stress-induced misfolding and aggregation. The heat shock protein of 90 kDa (HSP90) is the most abundant heat shock protein. While basal expression of HSP90 is essential for cell survival, in many tumors elevated HSP90 levels are found, which is often associated with bad prognosis. Therefore, HSP90 has emerged as a major target in tumor therapy. The HSP90 machinery is very complex in that it involves large conformational changes during the chaperoning cycle and a variety of co-chaperones. At the same time, this complexity offers a plethora of possibilities to interfere with HSP90 function. The best characterized class of HSP90 modulators are competitive inhibitors targeting the N-terminal ATP-binding pocket. Nineteen compounds of this class entered clinical trials. However, due to severe adverse effects, including induction of the heat shock response, no N-terminal inhibitor has been approved by the FDA so far. As alternatives, compounds commonly referred to as “C-terminal inhibitors” have been developed, either as natural product-based analogues or by rational design, which employ multiple mechanisms to modulate HSP90 function, including modulation of the interaction with co-chaperones, induction of conformational changes that influence the chaperoning cycle, or inhibition of C-terminal dimerization. In this review, we summarize the current development state of characteristic C-terminal inhibitors, with an emphasis on their (proposed) molecular modes of action and binding sites. 相似文献
3.
X. Preville P. Mehlen N. Fabre-Jonca S. Chaufour C. Kretz-Remy M. R. Michel A. -P. Arrigo 《Journal of biosciences》1996,21(2):221-234
The α-crystallin-related stress protein HSP27, which promotes cellular resistance to different types of stress, is constitutively
expressed during the growth of several primate tissue culture cells. Here, we report an analysis of the cellular localization
of this protein in CV-1 monkey cells. Following cell lysis and fractionation in the absence of detergent about 2 5 % of the
cellular content of HSP27 was recovered in the particu late fractions while the remaining of this protein was in the soluble
cytoplasmic fraction. This association of HSP27 with particulate fractions was no more observed when cells were lysed in the
presence of non-ionic detergent or when cells were pretreated with drugs, such as monensin and colcemid, that disrupt cytoskeletal
architecture. Immunofluorescence analysis revealed that HSP27 is concentrated in a polarized perinuclear zone of CV-1 cells
from where microtubules radiate. The particular locale of HSP27 was investigated in cells exposed to drugs or treatments,
such as monensin, colcemid, cold stess and serum starvation, that disrupt the cellular architecture of microtubules. A correlation
was observed between HSP27 cellular locale and microtubules integrity. Our results suggest a possible interaction of a fraction
of HSP27 with cytoplasmic organelles or structures, different from the Golgi apparatus, whose distribution depends upon the
organization of microtubules. 相似文献
4.
5.
Purification and characterization of porcine testis 90-kDa heat shock protein (HSP90) as a substrate for various protein kinases 总被引:1,自引:0,他引:1
Huang HC Yu JS Tsay CC Lin JH Huang SY Fang WT Liu YC Tzang BS Lee WC 《Journal of Protein Chemistry》2002,21(2):111-121
We purified a large quantity of HSP90 from porcine testis by hydroxylapatite (HA-HSP90) and SDS-PAGE/electroelution (eluted-HSP90) to explore the molecular mechanism of HSP90 phosphorylation affecting its metabolism. The purified HSP90 was used as an antigen to raise polyclonal antibodies in rabbits. Immunoblot analysis revealed that most purified HSP90 was HSP90. Compared with the commercial anti-HSP90 antibody, the polyclonal antibody raised in this study could specifically detect the testis HSP90 and immunoprecipitate HSP90 from tissue homogenates or cell extracts. Incubation of the purified HSP90 or HSP90 immunoprecipitated from extracts of human A431 cells, Balb/c 3T3 fibroblasts, and porcine testis with [-32P]ATP/Mg2+ resulted in phosphorylation of HSP90. However, the eluted-HSP90 lost its phosphorylation ability when incubated with [-32P]ATP·Mg2+ alone but could be phosphorylated by various protein kinases, including PKA, CKII, kinase FA/GSK-3 , and AK. The order of phosphorylation of HSP90 by these kinases is PKA = CKII > AK >> kinase FA/GSK-3 . 相似文献
6.
《Bioorganic & medicinal chemistry》2016,24(22):6082-6093
Based on the lead compound L-80 (compound 2), a potent heat shock protein 90 (HSP90) inhibitor, a series of C-ring truncated deguelin analogs were designed, synthesized and evaluated for Hypoxia Inducible Factor-1α (HIF-1α) inhibition as a primary screening method. Their structure–activity relationship was investigated in a systematic manner by varying the A/B ring, linker and D/E ring, respectively. Among the synthesized inhibitors, compound 5 exhibited potent HIF-1α inhibition in a dose-dependent manner and significant antitumor activity in human non-small cell lung carcinoma (H1299), with better activities than L-80. It also inhibited in vitro hypoxia-mediated angiogenic processes in human retinal microvascular endothelial cells (HRMEC). The docking study of 5 showed a similar binding mode as L-80: it occupied the C-terminal ATP-binding pocket of HSP90, indicating that the anticancer and antiangiogenic activities of 5 were derived from HIF-1α destabilization by inhibiting the C-terminal ATP-binding site of hHSP90. 相似文献
7.
8.
Variations on a theme: Combined molecular chaperone and proteolysis functions in Clp/HSP100 proteins
Adrian K. Clarke 《Journal of biosciences》1996,21(2):161-177
Most stress-inducible polypeptides are members of broader protein families that function either as molecular chaperones or
constituents of proteolytic pathways. These systems control many aspects of protein structure and function throughout the
cell under all types of growth regimes. The Clp/HSP1 00 protein family is a recently characterized representative, with constitutive
and stress-inducible members found in many different organisms and various intracellular locations. Besides being regulators
of energy-dependent proteolysis, Clp proteins may also function as molecular chaperones. Constitutive Clp proteins are involved
foremost in cellular protein maintenance and repair, in cooperation with other chaperone and proteolytic systems. At high
temperatures, additional Clp proteins are induced in response to rising levels of inactive polypeptides, resulting from either
biosynthetic errors, thermal denaturation and aggregation. Clp proteins presumably help to stabilize selected polypeptides
during severe thermal stress and enable resolubilization of non-functional protein aggregates, as well as promoting the degradation
of irreversibly damaged polypeptides. The union of chaperone and proteolytic regulatory functions in one molecule suggests
that certain Clp proteins play a decisive role in determining the destiny of proteins, not only during normal growth but also
under conditions of extreme stress. This review briefly covers recent findings on the diversity of Clp proteins and their
potential importance within the cell. 相似文献
9.
Among the monoclonal antibodies (mAb) against Toxoplasma gondii, mAb Tg485 specifically reacted with an 82-kDa cytoplasmic protein of tachyzoites. The protein was secreted from extracellular tachyzoites, but was not released into the parasitophorous vacuole after invasion. The cDNA fragment encoding the protein was obtained by screening a T. gondii cDNA expression library with Tg485. The full-length cDNA was amplified by the 5(')-RACE method and sequenced. The deduced amino acid sequence of the 82 kDa protein reacting with Tg485 revealed a polypeptide of 708 amino acids showing significant homology to the heat shock protein 90 (HSP90) family of other organisms, especially to those of apicomplexan species. Treatment with geldanamycin, a drug known to interfere with HSP90 function, did not affect the secretion of TgHSP90 from extracellular tachyzoites, but the entry of the tachyzoites into host cells and the intracellular growth of the parasite were significantly disturbed. 相似文献
10.
Effect of the 90 kDa heat shock protein, HSP90, on glucocorticoid receptor binding to DNA-cellulose 总被引:1,自引:0,他引:1
K J Howard C W Distelhorst 《Biochemical and biophysical research communications》1988,151(3):1226-1232
Glucocorticoid receptors in the IM-9 human lymphoblastoid cell line were affinity labeled with [3H]dexamethasone 21-mesylate and activated to a DNA-binding form by filtration through a Bio-Gel A-1.5m column. The 90 kDa heat shock protein, HSP90, was identified by labeling IM-9 cells with 35S-methionine at both 37 degrees C and 42 degrees C and purified to near homogeneity by sequential chromatography through DE52 and hydroxyapatite. Addition of purified HSP90 to activated, affinity labeled glucocorticoid receptors in a molecular ratio of 16 to 1 inhibited the binding of the receptors to DNA-cellulose. HSP90 did not affect the binding of other proteins to DNA-cellulose, indicating that the inhibitory effect of HSP90 was specific for the glucocorticoid receptor. These results suggest that HSP90 may associate with the glucocorticoid receptor, masking its DNA-binding site and thereby inhibiting receptor interaction with DNA. 相似文献
11.
Overexpression of heat shock protein 27 (HSP27) increases gemcitabine sensitivity in pancreatic cancer cells through S‐phase arrest and apoptosis
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Yang Guo Andreas Ziesch Sandra Hocke Eric Kampmann Stephanie Ochs Enrico N. De Toni Burkhard Göke Eike Gallmeier 《Journal of cellular and molecular medicine》2015,19(2):340-350
We previously established a role for HSP27 as a predictive marker for therapeutic response towards gemcitabine in pancreatic cancer. Here, we investigate the underlying mechanisms of HSP27‐mediated gemcitabine sensitivity. Utilizing a pancreatic cancer cell model with stable HSP27 overexpression, cell cycle arrest and apoptosis induction were analysed by flow cytometry, nuclear staining, immunoblotting and mitochondrial staining. Drug sensitivity studies were performed by proliferation assays. Hyperthermia was simulated using mild heat shock at 41.8°C. Upon gemcitabine treatment, HSP27‐overexpressing cells displayed an early S‐phase arrest subsequently followed by a strongly increased sub‐G1 fraction. Apoptosis was characterized by PARP‐, CASPASE 3‐, CASPASE 8‐, CASPASE 9‐ and BIM‐ activation along with a mitochondrial membrane potential loss. It was reversible through chemical caspase inhibition. Importantly, gemcitabine sensitivity and PARP cleavage were also elicited by heat shock‐induced HSP27 overexpression, although to a smaller extent, in a panel of pancreatic cancer cell lines. Finally, HSP27‐overexpressing pancreatic cancer cells displayed an increased sensitivity also towards death receptor‐targeting agents, suggesting another pro‐apoptotic role of HSP27 along the extrinsic apoptosis pathway. Taken together, in contrast to the well‐established anti‐apoptotic properties of HSP27 in cancer, our study reveals novel pro‐apoptotic functions of HSP27—mediated through both the intrinsic and the extrinsic apoptotic pathways—at least in pancreatic cancer cells. HSP27 could represent a predictive marker of therapeutic response towards specific drug classes in pancreatic cancer and provides a novel molecular rationale for current clinical trials applying the combination of gemcitabine with regional hyperthermia in pancreatic cancer patients. 相似文献
12.
Nuclear localization and the heat shock proteins 总被引:1,自引:0,他引:1
The highly conserved heat shock proteins (HSP) belong to a subset of cellular proteins that localize to the nucleus. HSPs
are atypical nuclear proteins in that they localize to the nucleus selectively, rather than invariably. Nuclear localization
of HSPs is associated with cell stress and cell growth. This aspect of HSPs is highly conserved with nuclear localization
occurring in response to a wide variety of cell stresses. Nuclear localization is likely important for at least some of the
heat shock proteins’ protective functions; little is known about the function of the heat shock proteins in the nucleus. Nuclear
localization is signalled by the presence of a basic nuclear localization sequence (NLS) within a protein. Though most is
known about HSP 72’s nuclear localization, the NLS(s) has not been definitively identified for any of the heat shock proteins.
Likely more is involved than presence of a NLS; since the heat shock proteins only localize to the nucleus under selective
conditions, nuclear localization must be regulated. HSPs also function as chaperons of nuclear transport, facilitating the
movement of other macromolecules across the nuclear membrane. The mechanisms involved in chaperoning of proteins by HSPs into
the nucleus are still being identified. 相似文献
13.
The technique of fine needle aspiration (FNA) is increasingly used in the investigation of breast abnormalities both palpable and impalpable. However, up to 20% of aspirates fall into two categories which require further investigation, because they either show cytological atypia or exhibit features which are suspicious of malignancy (reporting categories C3 and C4). The usefulness of the 27-kD heat shock protein (HSP27) expression in refining these categories of suspicion, and possibly in predicting malignancy, was investigated using an established immunocytochemical staining procedure. Positive HSP27 staining was shown by 73.1% of C4 and 33.3% of C3 FNAs. Statistical analysis showed a significant difference between the results obtained for the C3 and C4 FNAs. 相似文献
14.
Robert V. Blackburn Sandra S. Galoforo Christine M. Berns Peter M. Corry Yong J. Lee 《Journal of thermal biology》1996,21(5-6):365-372
- 1. 1. We examined rodent cells transfected with an expression plasmid encoding a human small heat shock protein for possible compensatory expression of endogenous heat shock genes. For these investigations, human hsp27 was transfected into CHO cells which express endogenous HSP25.
- 2. 2. Both endogenous HSP25 and transfected HSP27 were expressed and multiple phosphorylated isoforms were detected upon exposure to thermal stress.
- 3. 3. Levels of endogenous HSP70 and HSP25 did not appear to be altered by expression of the heterologous heat shock protein.
- 4. 4. These results suggest that compensatory interactions are not exhibited in the expression of the heat shock genes examined, and that independent regulation may exist not only between the large and small heat shock proteins, but also between individual small heat shock proteins as well.
15.
16.
Ho Shin Kim Van-Hai Hoang Mannkyu Hong Kyung Chul Kim Jihyae Ann Cong-Truong Nguyen Ji Hae Seo Hoon Choi Jun Yong Kim Kyu-Won Kim Woong Sub Byun Sangkook Lee Seungbeom Lee Young-Ger Suh Jie Chen Hyun-Ju Park Tae-Min Cho Ji Young Kim Jeewoo Lee 《Bioorganic & medicinal chemistry》2019,27(7):1370-1381
On the basis of deguelin, a series of the B,C-ring truncated surrogates with N-substituted amide linkers were investigated as HSP90 inhibitors. The structure activity relationship of the template was studied by incorporating various substitutions on the nitrogen of the amide linker and examining their HIF-1α inhibition. Among them, compound 57 showed potent HIF-1α inhibition and cytotoxicity in triple-negative breast cancer lines in a dose-dependent manner. Compound 57 downregulated expression and phosphorylation of major client proteins of HSP90 including AKT, ERK and STAT3, indicating that its antitumor activity was derived from the inhibition of HSP90 function. The molecular modeling of 57 demonstrated that 57 bound well to the C-terminal ATP-binding pocket in the open conformation of the hHSP90 homodimer with hydrogen bonding and pi-cation interactions. Overall, compound 57 is a potential antitumor agent for triple-negative breast cancer as a HSP90 C-terminal inhibitor. 相似文献
17.
Identification of enteric pathogens by heat shock protein 60 kDa (HSP60) gene sequences 总被引:8,自引:0,他引:8
A highly specific and reproducible approach for the simultaneous detection of enteric pathogenic bacteria was developed using bacterial hsp60 gene and molecular biological tools. A single pair of universal primers was derived from the highly conserved sequence of hsp60 genes encompassing a 600-bp hypervariable region. PCR amplification followed by either dot blot hybridization or restriction enzyme digestion performed on 38 enteric bacteria indicated that this approach could differentiate not only different genera such as Campylobacter, Yersinia and Vibrio, but also species that are closely related genetically, such as between C. jejuni and C. coli, or between Salmonella and Shigella or Escherichia coli. 相似文献
18.
19.
Montagna GN Buscaglia CA Münter S Goosmann C Frischknecht F Brinkmann V Matuschewski K 《The Journal of biological chemistry》2012,287(4):2410-2422
Plasmodium sporozoites, single cell eukaryotic pathogens, use their own actin/myosin-based motor machinery for life cycle progression, which includes forward locomotion, penetration of cellular barriers, and invasion of target cells. To display fast gliding motility, the parasite uses a high turnover of actin polymerization and adhesion sites. Paradoxically, only a few classic actin regulatory proteins appear to be encoded in the Plasmodium genome. Small heat shock proteins have been associated with cytoskeleton modulation in various biological processes. In this study, we identify HSP20 as a novel player in Plasmodium motility and provide molecular genetics evidence for a critical role of a small heat shock protein in cell traction and motility. We demonstrate that HSP20 ablation profoundly affects sporozoite-substrate adhesion, which translates into aberrant speed and directionality in vitro. Loss of HSP20 function impairs migration in the host, an important sporozoite trait required to find a blood vessel and reach the liver after being deposited in the skin by the mosquito. Our study also shows that fast locomotion of sporozoites is crucial during natural malaria transmission. 相似文献
20.
M K Ruohonen-Lehto M F Rothschild R G Larson M K Ruohonen-Lehto M F Rothschild R G Larson 《Animal genetics》1993,24(1):67-68
Pigs from a population consisting of eight US breeds or strains and three Chinese breeds were examined by restriction fragment length polymorphism (RFLP) analysis of the heat shock protein HSP70 gene(s). Limited polymorphisms with PstI and PvuII restriction enzymes were observed, but there were no polymorphisms with BomIII and BglI. 相似文献