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1.
Lipids Health Dis ; 19(1): 195, 2020 Aug 23.
Article in English | MEDLINE | ID: mdl-32829709

ABSTRACT

BACKGROUND: The regulation of exocytosis is physiologically vital in cells and requires a variety of distinct proteins and lipids that facilitate efficient, fast, and timely release of secretory vesicle cargo. Growing evidence suggests that regulatory lipids act as important lipid signals and regulate various biological processes including exocytosis. Though functional roles of many of these regulatory lipids has been linked to exocytosis, the dynamic behavior of these lipids during membrane fusion at sites of exocytosis in cell culture remains unknown. METHODS: Total internal reflection fluorescence microscopy (TIRF) was used to observe the spatial organization and temporal dynamics (i.e. spatial positioning and timing patterns) of several lipids, and accessory proteins, like lipid kinases and protein kinases, in the form of protein kinase C (PRKC) associated with sites of exocytosis of matrix metalloproteinase-9 (MMP-9) in living MCF-7 cancer cells. RESULTS: Following stimulation with phorbol myristate acetate (PMA) to promote exocytosis, a transient accumulation of several distinct regulatory lipids, lipid kinases, and protein kinases at exocytic sites was observed. This transient accumulation centered at the time of membrane fusion is followed by a rapid diffusion away from the fusion sites. Additionally, the synthesis of these regulatory lipids, degradation of these lipids, and the downstream effectors activated by these lipids, are also achieved by the recruitment and accumulation of key enzymes at exocytic sites (during the moment of cargo release). This includes key enzymes like lipid kinases, protein kinases, and phospholipases that facilitate membrane fusion and exocytosis of MMP-9. CONCLUSIONS: This work suggests that these regulatory lipids and associated effector proteins are locally synthesized and/or recruited to sites of exocytosis, during membrane fusion and cargo release. More importantly, their enrichment at fusion sites serves as an important spatial and temporal organizing "element" defining individual exocytic sites.


Subject(s)
Matrix Metalloproteinase 9/metabolism , Animals , Blotting, Western , Exocytosis/genetics , Exocytosis/physiology , Humans , MCF-7 Cells , Microscopy, Fluorescence , Protein Kinase C/metabolism , Secretory Vesicles/metabolism
2.
Trends Cancer ; 6(4): 273-276, 2020 04.
Article in English | MEDLINE | ID: mdl-32209442

ABSTRACT

For metastasis to occur, cancer cells must exocytose proteases, like matrix metalloproteinases (MMPs), that are key in extracellular matrix (ECM) degradation. Growing evidence suggests that cancer cells use distinct spatial and temporal clustering patterns or organizing 'elements' that facilitate secretory vesicle fusion and the subsequent exocytosis of proteins that contribute to metastasis.


Subject(s)
Exocytosis , Extracellular Matrix/pathology , Neoplasm Metastasis/pathology , Actin Cytoskeleton/metabolism , Cell Membrane/metabolism , Humans , Lipid Metabolism , Matrix Metalloproteinases/metabolism , Secretory Vesicles/metabolism , rab27 GTP-Binding Proteins/metabolism
3.
J Gen Physiol ; 151(12): 1386-1403, 2019 12 02.
Article in English | MEDLINE | ID: mdl-31676484

ABSTRACT

Altered regulation of exocytosis is an important mechanism controlling many diseases, including cancer. Defects in exocytosis have been implicated in many cancer cell types and are generally attributed to mutations in cellular transport, trafficking, and assembly of machinery necessary for exocytosis of secretory vesicle cargo. In these cancers, up-regulation of trafficking and secretion of matrix metalloproteinase-9 (MMP-9), a proteolytic enzyme, is responsible for degrading the extracellular matrix, a necessary step in tumor progression. Using TIRF microscopy, we identified proteins associated with secretory vesicles containing MMP-9 and imaged the local dynamics of these proteins at fusion sites during regulated exocytosis of MMP-9 from MCF-7 breast cancer cells. We found that many regulators of exocytosis, including several Rab GTPases, Rab effector proteins, and SNARE/SNARE modulator proteins, are stably assembled on docked secretory vesicles before exocytosis. At the moment of fusion, many of these components are quickly lost from the vesicle, while several endocytic proteins and lipids are simultaneously recruited to exocytic sites at precisely that moment. Our findings provide insight into the dynamic behavior of key core exocytic proteins, accessory proteins, lipids, and some endocytic proteins at single sites of secretory vesicle fusion in breast cancer cells.


Subject(s)
Breast Neoplasms/metabolism , Exocytosis/physiology , Matrix Metalloproteinase 9/metabolism , Biological Transport/physiology , Cell Line, Tumor , Cell Membrane/metabolism , Cell Membrane/physiology , Female , Humans , MCF-7 Cells , Membrane Fusion/physiology , SNARE Proteins/metabolism , Secretory Vesicles/metabolism , rab GTP-Binding Proteins/metabolism
4.
PLoS One ; 10(3): e0117495, 2015.
Article in English | MEDLINE | ID: mdl-25798887

ABSTRACT

For metastasis to occur cells must communicate with to their local environment to initiate growth and invasion. Exosomes have emerged as an important mediator of cell-to-cell signalling through the transfer of molecules such as mRNAs, microRNAs, and proteins between cells. Exosomes have been proposed to act as regulators of cancer progression. Here, we study the effect of exosomes on cell migration, an important step in metastasis. We performed cell migration assays, endocytosis assays, and exosome proteomic profiling on exosomes released from three breast cancer cell lines that model progressive stages of metastasis. Results from these experiments suggest: (1) exosomes promote cell migration and (2) the signal is stronger from exosomes isolated from cells with higher metastatic potentials; (3) exosomes are endocytosed at the same rate regardless of the cell type; (4) exosomes released from cells show differential enrichment of proteins with unique protein signatures of both identity and abundance. We conclude that breast cancer cells of increasing metastatic potential secrete exosomes with distinct protein signatures that proportionally increase cell movement and suggest that released exosomes could play an active role in metastasis.


Subject(s)
Biomarkers, Tumor/metabolism , Breast Neoplasms/metabolism , Breast Neoplasms/pathology , Cell Movement , Cell Proliferation , Exosomes/metabolism , Proteomics , Blotting, Western , Cell Communication , Chromatography, Liquid , Female , Humans , Tandem Mass Spectrometry , Tumor Cells, Cultured , Wound Healing
5.
J Cell Biol ; 194(1): 77-87, 2011 Jul 11.
Article in English | MEDLINE | ID: mdl-21746852

ABSTRACT

Mammals lacking BLOC-3 have impaired formation of melanosomes, a type of lysosome-related organelle (LRO), and, in earlier work, we found that a subunit of the BLOC-3 complex inhibits loading of Argonaute (Ago) proteins with small ribonucleic acids (RNAs) in Drosophila melanogaster cells. Small RNAs such as small interfering RNAs (siRNAs) direct Ago proteins to repress the stability of messenger RNA transcripts. In this paper, we show that BLOC-3 is required for biogenesis of Drosophila LROs called pigment granules. Other complexes that sort cargo to pigment LROs also negatively regulate siRNA activity. However, regulation is not obligately linked to biogenesis of LROs but instead to specific cargo-sorting processes. Negative regulation is also not linked to sorting into all LROs but only a specific class of pigment LRO. Thus, regulation of siRNA activity is tied to sorting of specific types of cargo to particular LROs.


Subject(s)
Drosophila Proteins/genetics , Gene Silencing , Lysosomes/metabolism , Organelles/metabolism , Pigments, Biological/metabolism , RNA, Messenger/genetics , RNA, Small Interfering/metabolism , RNA-Induced Silencing Complex/genetics , Animals , Argonaute Proteins , Drosophila melanogaster
6.
J Mol Biol ; 341(2): 389-403, 2004 Aug 06.
Article in English | MEDLINE | ID: mdl-15276831

ABSTRACT

The two forms of the hepatitis delta virus ribozyme are derived from the genomic and antigenomic RNA strands of the human hepatitis delta virus (HDV), where they serve a crucial role in pathogen replication by catalyzing site-specific self-cleavage reactions. The HDV ribozyme requires divalent metal ions for formation of its tertiary structure, consisting of a tight double-nested pseudoknot, and for efficient self- (or cis-) cleavage. Comparison of recently solved crystal structures of the cleavage precursor and 3' product indicates that a significant conformational switch is required for catalysis by the genomic HDV ribozyme. Here, we have used the lanthanide metal ion terbium(III) to footprint the precursor and product solution structures of the cis-acting antigenomic HDV ribozyme. Inhibitory Tb(3+) binds with high affinity to similar sites on RNA as Mg(2+) and subsequently promotes slow backbone scission. We find subtle, yet significant differences in the terbium(III) footprinting pattern between the precursor and product forms of the antigenomic HDV ribozyme, consistent with differences in conformation as observed in the crystal structures of the genomic ribozyme. In addition, UV melting profiles provide evidence for a less tight tertiary structure in the precursor. In both the precursor and product we observe high-affinity terbium(III) binding sites in joining sequence J4/2 (Tb(1/2) approximately 4 microM) and loop L3, which are key structural components forming the catalytic core of the HDV ribozyme, as well as in several single-stranded regions such as J1/2 and the L4 tetraloop (Tb(1/2) approximately 50 microM). Sensitized luminescence spectroscopy confirms that there are at least two affinity classes of Tb(3+) binding sites. Our results thus demonstrate that a significant conformational change accompanies catalysis in the antigenomic HDV ribozyme in solution, similar to the catalytic conformational switch observed in crystals of the genomic form, and that structural and perhaps catalytic metal ions bind close to the catalytic core.


Subject(s)
DNA Footprinting , Hepatitis Delta Virus/enzymology , RNA, Catalytic/chemistry , RNA, Viral/chemistry , Terbium/metabolism , Base Pairing , Base Sequence , Binding Sites , Catalytic Domain , Hepatitis Delta Virus/chemistry , Humans , Molecular Sequence Data , Nucleic Acid Conformation , RNA, Catalytic/metabolism , RNA, Viral/genetics , RNA, Viral/metabolism , Structure-Activity Relationship , Terbium/pharmacology
7.
Biochemistry ; 43(28): 8935-45, 2004 Jul 20.
Article in English | MEDLINE | ID: mdl-15248751

ABSTRACT

The ability of divalent metal ions to participate in both structure formation and catalytic chemistry of RNA enzymes (ribozymes) has made it difficult to separate their cause and effect in ribozyme function. For example, the recently solved crystal structures of precursor and product forms of the cis-cleaving genomic hepatitis delta virus (HDV) ribozyme show a divalent metal ion bound in the active site that is released upon catalysis due to an RNA conformational change. This conformational switch is associated with a repositioning of the catalytically involved base C75 in the active-site cleft, thus controlling catalysis. These findings confirm previous data from fluorescence resonance energy transfer (FRET) on a trans-acting form of the HDV ribozyme that found a global conformational change to accompany catalysis. Here, we further test the conformational switch model by measuring the Mg(2+) dependence of the global conformational change of the trans-acting HDV ribozyme, using circular dichroism and time-resolved FRET as complementary probes of secondary and tertiary structure formation, respectively. We observe significant differences in both structure and Mg(2+) affinity of the precursor and product forms, in the presence and absence of 300 mM Na(+) background. The precursor shortens while the product extends with increasing Mg(2+) concentration, essentially amplifying the structural differences observed in the crystal structures. In addition, the precursor has an approximately 2-fold and approximately 13-fold lower Mg(2+) affinity than the product in secondary and tertiary structure formation, respectively. We also have compared the C75 wild-type with the catalytically inactive C75U mutant and find significant differences in global structure and Mg(2+) affinity for both their precursor and product forms. Significantly, the Mg(2+) affinity of the C75 wild-type is 1.7-2.1-fold lower than that of the C75U mutant, in accord with the notion that C75 is essential for a catalytic conformational change that leads to a decrease in the local divalent metal ion affinity and release of a catalytic metal. Thus, a consistent picture emerges in which divalent metal ions and RNA functional groups are intimately intertwined in affecting structural dynamics and catalysis in the HDV ribozyme.


Subject(s)
Hepatitis Delta Virus/enzymology , Magnesium/pharmacology , RNA, Catalytic/chemistry , Catalysis , Hepatitis Delta Virus/genetics , Magnesium/chemistry , Models, Molecular , Mutation , Nucleic Acid Conformation/drug effects , RNA, Catalytic/genetics
8.
J Am Chem Soc ; 125(46): 13972-3, 2003 Nov 19.
Article in English | MEDLINE | ID: mdl-14611229

ABSTRACT

The exchange of deuterium for hydrogen in water often produces solvent kinetic isotope effects (KSIEs) on the rate constants associated with enzyme reactions, including those catalyzed by RNA. Recently, KSIEs have been used to show that proton transfer occurs in the rate-limiting step of cleavage by the hepatitis delta virus (HDV) ribozyme and other catalytic RNAs. To test the underlying assumption that KSIEs are related to the chemistry step of ribozyme-mediated cleavage reactions, we developed fluorescence resonance energy transfer assays to measure KSIEs on the rate constants of conformational changes associated with substrate binding and dissociation by a trans-acting HDV ribozyme. We observe comparable KSIEs ( approximately 2-2.5-fold) of rate constants of conformational change and cleavage, while proton inventory experiments are consistent with a shift in the ensemble of transition states upon increase of D2O in the solvent. Taken together, these results challenge the common assumption that pL profiles of RNA-catalyzed reactions yielding a pKa and KSIE necessarily provide evidence for an ionization (chemistry) step to be rate-limiting. They also suggest that an unusual proton inventory may provide a signature for a conformational change contributing to the rate-limiting step.


Subject(s)
Hepatitis Delta Virus/genetics , RNA, Catalytic/chemistry , RNA, Viral/chemistry , Base Sequence , Deuterium Exchange Measurement , Hepatitis Delta Virus/chemistry , Kinetics , Nucleic Acid Conformation
9.
Curr Protoc Nucleic Acid Chem ; Chapter 6: Unit 6.8, 2003 Aug.
Article in English | MEDLINE | ID: mdl-18428913

ABSTRACT

The function of an RNA molecule is determined by its overall secondary and tertiary structure. The tertiary structure is facilitated and stabilized by the interaction with metal ions. The current chapter offers a detailed protocol on the use of the lanthanide metal ion terbium(III) as a powerful probe of RNA structure and metal-binding properties. When incubating RNA with low (micromolar) concentrations of terbium(III), specific backbone scission by partially deprotonated aqueous terbium(III) complexes can be used to detect high-affinity metal-binding sites, while incubation with high (millimolar) terbium(III) concentrations cleaves the RNA backbone preferentially at structurally accessible regions, providing a footprint of the RNA secondary and tertiary structure.


Subject(s)
Metals/metabolism , RNA/chemistry , Sequence Analysis, RNA/methods , Terbium/pharmacology , Base Sequence , Binding Sites , Models, Biological , Molecular Sequence Data , Nucleic Acid Conformation , RNA/metabolism , RNA Probes/chemistry , Radioisotopes/pharmacology
10.
Biochemistry ; 41(40): 12051-61, 2002 Oct 08.
Article in English | MEDLINE | ID: mdl-12356305

ABSTRACT

The hepatitis delta virus (HDV) is a human pathogen and satellite RNA of the hepatitis B virus. It utilizes a self-cleaving catalytic RNA motif to process multimeric intermediates in the double-rolling circle replication of its genome. Previous kinetic analyses have suggested that a particular cytosine residue (C(75)) with a pK(a) close to neutrality acts as a general acid or base in cleavage chemistry. The crystal structure of the product form of a cis-acting HDV ribozyme shows this residue positioned close to the 5'-OH leaving group of the reaction by a trefoil turn in the RNA backbone. By modifying G(76) of the trefoil turn of a synthetic trans-cleaving HDV ribozyme to the fluorescent 2-aminopurine (AP), we can directly monitor local conformational changes in the catalytic core. In the ribozyme-substrate complex (precursor), AP fluorescence is strongly quenched, suggesting that AP(76) is stacked with other bases and that the trefoil turn is not formed. In contrast, formation of the product complex upon substrate cleavage or direct product binding results in a significant increase in fluorescence, consistent with AP(76) becoming unstacked and solvent-exposed as evidenced in the trefoil turn. Using AP fluorescence and fluorescence resonance energy transfer (FRET) in concert, we demonstrate that this local conformational change in the trefoil turn is kinetically coincidental with a previously observed global structural change of the ribozyme. Our data show that, at least in the trans-acting HDV ribozyme, C(75) becomes positioned for reaction chemistry only along the trajectory from precursor to product.


Subject(s)
Hepatitis Delta Virus/metabolism , RNA, Catalytic/metabolism , RNA, Viral/metabolism , 2-Aminopurine/metabolism , Binding Sites , Catalytic Domain , Hepatitis Delta Virus/enzymology , Hepatitis Delta Virus/genetics , Hydrogen-Ion Concentration , Kinetics , Nucleic Acid Conformation , Spectrometry, Fluorescence , Transcriptional Activation
11.
Biochemistry ; 41(3): 730-40, 2002 Jan 22.
Article in English | MEDLINE | ID: mdl-11790094

ABSTRACT

The hepatitis delta virus (HDV), an infectious human pathogen and satellite of hepatitis B virus, leads to intensified disease symptoms, including progression to liver cirrhosis. Both the circular RNA genome of HDV and its complementary antigenome contain the same cis-cleaving catalytic RNA motif that plays a crucial role in virus replication. Previously, the high-resolution crystal structure of the product form of a cis-acting genomic HDV ribozyme has been determined, while a trans-acting version of the ribozyme was used to dissect the cleavage reaction pathway. Using fluorescence resonance energy transfer (FRET) on a synthetic trans-cleaving form of the ribozyme, we are able to directly observe substrate binding (at a rate constant k(on) of 7.8 x 10(6) M(-1) min(-1) at pH 7.5, 11 mM MgCl(2), and 25 degrees C) and dissociation (at 0.34 min(-1)). Steady-state and time-resolved FRET experiments in solution and in nondenaturing gels reveal that the substrate (precursor) complex is slightly more compact (by approximately 3 A) than the free ribozyme, yet becomes significantly extended (by approximately 15 A) upon cleavage and product complex formation. We also find that trans cleavage is characterized by a high transition-state entropy (-26 eu). We propose that the significant global conformational change that we observe between the precursor and product structures occurs on the reaction trajectory into a constrained product complex-like transition state. Our observations may present the structural basis of the recently described utilization of intrinsic substrate binding energy to the overall catalytic rate enhancement by the trans-acting HDV ribozyme.


Subject(s)
Hepatitis Delta Virus/physiology , RNA, Catalytic/chemistry , Base Sequence , Calcium/pharmacology , Genome, Viral , Hepatitis Delta Virus/genetics , Humans , Hydrogen-Ion Concentration , Kinetics , Manganese/pharmacology , Models, Molecular , Molecular Sequence Data , Nucleic Acid Conformation , Oligoribonucleotides/chemistry , Phosphorylation , RNA, Catalytic/metabolism , Substrate Specificity , Thermodynamics , Virus Replication
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