ライフサイエンスコーパス: fusion

1 protein that is required to elicit membrane fusion.

2 ggering conformational changes essential for fusion.

3 1 EML4-ALK gene fusion and 1 KIF5B-RET gene fusion.

4 se lysines contributed to gB/gH-gL cell-cell fusion.

5 cristae structure and mitochondrial network fusion.

6 satellite cell proliferation, activation and fusion.

7 n a method developed to study yeast vacuolar fusion.

8 is required for outer mitochondrial membrane fusion.

9 expression with dysregulated gBcyt-mediated fusion.

10 ing the mechanism of virus-mediated membrane fusion.

11 vivo in a melanoma cells harboring the BRAF fusion.

12 y few milliseconds delay between docking and fusion.

13 appear to be able to regulate yeast vacuolar fusion.

14 s to host cell receptors to mediate membrane fusion.

15 an significantly enhance, cell-cell membrane fusion.

16 ctors that control mitochondrial fission and fusion.

17 (TGN) to endosome traffic and TGN homotypic fusion.

18 er functions at the plasma membrane to drive fusion.

19 , and low doses of methanol mildly inhibited fusion.

20 ndergo determination and eventually cellular fusion.

21 is sufficient to promote mammalian cell-cell fusion.

22 tate at the time of virus-host cell membrane fusion.

23 roteases to mediate virus-cell and cell-cell fusion.

24 olar compartment (PVC) and for TGN homotypic fusion.

25 r suppressing TMEM16F inhibited Env-mediated fusion.

26 myogenic development by repressing myoblast fusion.

27 ng 1 eye and with strategies used to recover fusion.

28 networks constantly remodeled by fission and fusion.

29 A receptor with a cytochrome b562-RIL (BRIL) fusion (A2AR-BRIL) in the intracellular loop 3 (ICL3) wa

30 An increase in PV-endosomal/lysosomal fusion accompanied by augmented PV degradation in Wnt5a-

31 Whereas reduced predocked SG fusion accounted for reduced first-phase GSIS, selective

32 microscopy, we now show that, after granule fusion, actin recovers at the synapse and no further sec

33 ndicated mitochondrial network formation and fusion activity in ventricular cardiomyocytes.

34 heptad-repeat domain, is required for normal fusion activity with HOPS.

35 Using a novel FUSION algorithm, we integrate all data creating a compr

36 However, fusion alone is not sufficient.

37 expression of EP300-ZNF384 and CREBBP-ZNF384 fusion altered differentiation of mouse hematopoietic st

38 d 1 MET mutation, as well as 1 EML4-ALK gene fusion and 1 KIF5B-RET gene fusion.

39 NARE) proteins play a major role in membrane fusion and contribute to cell expansion, signaling, and

40 called autophagosomes, followed by lysosomal fusion and degradation.

41 Both fusion and fission of lysosomal membrane are accompanied

42 n WQ in blocking HIV-1 Env-mediated membrane fusion and had higher levels of binding affinity with NH

43 d PS strongly promotes Env-mediated membrane fusion and HIV-1 infection.

44 Cellular localization of the MybA::Gfp fusion and immunoprecipitation of the MybA::Gfp or MybA:

45 ane-bound mediator of mitochondrial membrane fusion and inter-organelle communication.

46 the mechanisms by which it controls vesicle fusion and plasticity are not well understood.

47 n and membrane solubilization of an MsrQ-GFP fusion and set up a purification scheme allowing the pro

48 ork maintenance requires continuous membrane fusion and that Yop1p favours the generation of highly c

49 -helix bundle that mediates synaptic vesicle fusion and used it to study vesicle fusion to a tethered

50 no residence time on plasma membrane before fusion and, to a lesser extent, also the predocked SGs.

51 Gene fusions and duplications have further shaped the composi

52 nt-derived xenograft models (PDX) with RSPO3 fusions and in tumors with common CRC mutations such as

53 angements, DNA amplifications and transcript fusions and predictive of telomerase activity.

54 rafish embryogenesis coincides with myoblast fusion, and genetic deletion of myomixer using CRISPR/Ca

55 uired Fc gamma receptor engagement, bypassed fusion, and initiated signaling through both TLR7 and TL

56 ct membrane curvature and vesicle formation, fusion, and trafficking.

57 by progressive vertebral, carpal and tarsal fusions, and mild short stature.

58 immunization of mice with the recombinant Ct fusion antigen CTH522.

59 ive metrics to evaluate the results of image fusion are also discussed.

60 for simultaneous detection of multiple gene fusions are limited by tedious and prolonged experimenta

61 re we report that, unlike BRAF fusions, CRAF fusions are unresponsive to both generations of RAFi, ve

62 ole in the induction of osteoclast (OC) cell fusion, as well as DC-mediated immune regulation.

63 Using a synchronized fusion assay, we demonstrated that myomaker functions at

64 e, using a reconstituted "flipped" cell-cell fusion assay, we show that lipid-anchored STX11 and its

65 e fusion levels in an in vitro gB/gH-gL cell fusion assay.

66 in Saccharomyces cerevisiae Using cell-free fusion assays and light microscopy, we find that GTPase

67 Cell-cell fusion assays show a strain-independent failure of fusio

68 e results imply that SERINC5 restricts HIV-1 fusion at a step prior to small pore formation by select

69 providing mechanistic insight into compound fusion at ribbon-style synapses.

70 y expressing truncated versions of SS4 and a fusion between the N-terminal region of SS4 and GS in th

71 subsequently undergoes a series of breakage-fusion-bridge (BFB) cycles.

72 generates palindromic DNA, such as Breakage-Fusion-Bridge cycles.

73 inase Yck3, is dispensable for tethering and fusion but can affect tethering if phosphorylated.

74 panol enhanced fusion, butanol also enhanced fusion but was less potent, and low doses of methanol mi

75 found to be required for virus-mediated cell fusion, but only for mutants that harbor syncytial mutat

76 Ethanol and propanol enhanced fusion, butanol also enhanced fusion but was less potent

77 -Ubp2-Rsp5 crosstalk regulates mitochondrial fusion by coordinating an intricate balance between Fzo1

78 ction with M1 protein, while the stunting of fusion by deacylated HA acting in isolation may be balan

79 n1 in the chick otic vesicle prevented canal fusion by inhibiting apoptosis.

80 of yeast vacuolar SNAREs into complexes for fusion can be studied in chemically defined reactions.

81 rapeutic window for LGK974 treatment of RSPO-fusion cancers.

82 tochondrial fractions suggested that loss of fusion capacity targets fragmented mitochondria to the p

83 We conclude that an entire fusion cascade can be controlled by a GEF.

84 At the ZCF and during fusion, Cdc42p and Fus2p colocalized.

85 Namely, 5RK acts as a fusion clamp, making release dependent on stimulation by

86 ine substitutions induced a 440% increase in fusion compared to that of the wild-type gBcyt while arg

87 the ribbon-style active zones were initially fusion competent.

88 priming step that renders synaptic vesicles fusion-competent, and their genetic elimination causes a

89 ansmembrane proteins that comprise the entry fusion complex (EFC), and had increased amounts of unpro

90 pre-fusion state and triggering to the post-fusion conformation is important for understanding F pro

91 tested in a paper-based assay format using a fusion construct consisting of an rcSso7d binding module

92 f mitochondria and mitochondrial fission and fusion contribute to this rejuvenation, but local protei

93 sms that regulate rates of crypt fission and fusion could provide insights into intestinal adaptation

94 ope, which is responsible for attachment and fusion, could aid in the development of a vaccine and/or

95 Here we report that, unlike BRAF fusions, CRAF fusions are unresponsive to both generatio

96 However, dispersion of fusion dates is common and interpretation is complicated

97 ression of the viral glycoprotein, but not a fusion defective mutant, is sufficient to cause CO2 sens

98 In conclusion, BRAF fusions define a new molecular subset of PMM that can be

99 atients with MPNs, detection of the BCR-ABL1 fusion delineates chronic myeloid leukemia from classic

100 candidate materials will ensure that future fusion devices design components with optimal thermal st

101 into heterodimers, whereas the interparticle fusion drives assembled HNCs into ordered heterorod arra

102 Here we report that formation of the pre-fusion Env-CD4-coreceptor complexes triggers non-apoptot

103 Finally, we show that this fusion event is prevented by inhibition of the IKKbeta2

104 image analysis to detect individual vesicle fusion events with approximately 27 nm localization prec

105 Furthermore, we show that these novel GSDMD fusions execute inflammasome-dependent pyroptotic cell d

106 Virion-cell and cell-cell fusion experiments revealed that LY6E promotes membrane

107 eloped previously as a vector expressing RSV fusion (F) protein to confer bivalent protection against

108 uce a method, which we refer to as colloidal fusion, for fabricating functional patchy particles in a

109 Hyperfusogenic gB could restore the fusion function with PILRalpha when a gD constructed con

110 s a proto-oncogene well known as part of the fusion gene BCR-ABL1 in the Philadelphia chromosome of l

111 isease driven by expression of the oncogenic fusion gene PAX3-FOXO1A.

112 search options and graphic representation of fusion gene structure.

113 study, we analyzed the status of TMPRSS2-ERG fusion genes and interstitial genes in tumors from a lar

114 We also identify recurrent fusion genes that significantly impact both progression-

115 The fusion glycoprotein (F) of RSV in either its postfusion

116 tive guidance, (b) biopsy with MR imaging/US fusion guidance, and (c) in-gantry MR imaging-guided bio

117 On the other hand, GPCR-G protein fusions have been used extensively to understand the sel

118 rigins and the convergent reduction of notal fusion in more derived clades, presumably due to wing ro

119 analyses, we show that mitochondrial fission/fusion in reactive microglia is differentially regulated

120 during homotypic vacuolar lysosome membrane fusion in Saccharomyces cerevisiae Using cell-free fusio

121 ion in POMC neurons, promoting mitochondrial fusion in their neurites, and increasing POMC neuronal f

122 ic mutant of SNAP23 can mediate homotypic SG fusion in triggered cells.

123 a transmembrane domain, can support membrane fusion in vivo is uncertain, as is the precise role of M

124 g CRISPR/Cas9 mutagenesis abolishes myoblast fusion in vivo.

125 fy somatic SNVs, small indels, CNVs and gene fusions in 508 tumor-related genes.

126 , we identified several novel oncogenic gene fusions in colorectal cancer that may drive malignant de

127 breakpoints of TMEM135-CCDC67 and MAN2A1-FER fusions in human prostate cancer or hepatocellular carci

128 e, called INTEGRATE-Neo, by identifying gene fusions in prostate cancers that may produce neoantigens

129 al basis for several activities required for fusion, including a C2B surface implicated in SNARE comp

130 ate and harbour organized sarcomeres but are fusion-incompetent.

131 tion into the target cell membrane increases fusion inhibitor potency.

132 n previous work, we have generated potent MV fusion inhibitors by dimerizing the F-derived peptides a

133 We hypothesize that the fusion inhibitors could interfere with the structural ch

134 known as the classic drug target to develop fusion inhibitors derived from the gp41 CHR.

135 inding site of these aniline-based influenza fusion inhibitors, which significantly overlaps with the

136 he potency of the existing peptide-based HIV fusion inhibitors.

137 est a new framework for developing effective fusion inhibitory peptides.

138 ructure that can be specifically targeted by fusion-inhibitory peptides.

139 sed and nonfused SMAs, we show that the ring-fusion introduces several beneficial effects on the prop

140 We also found a novel fusion involving USP9X-ERAS formed by chromothripsis and

141 se tumors also frequently displayed ERG gene fusions involving alternative 5'-partners to TMPRSS2, sp

142 Myoblast fusion is an indispensable step for skeletal muscle deve

143 Whether myomaker-mediated heterologous fusion is functional in vivo and whether the newly intro

144 We found treatment of MLL-fusion leukaemia cells (MV4;11 cell line) with the BET b

145 chromatin as an effective treatment for MLL-fusion leukaemia".

146 le arginine substitutions had wild-type-like fusion levels in an in vitro gB/gH-gL cell fusion assay.

147 increase the activation energy required for fusion, likely through an increase in membrane fluidity.

148 The fusion loop is also a target of pan-flavivirus antibodie

149 s identified within the epitopes in the EDII fusion loop likely explain the sequence and antigenic co

150 synthetic peptide corresponding to the HAP2 fusion loop was found to interact directly with model me

151 by patients with intermittent exotropia when fusion loss occurs spontaneously and to compare them wit

152 quisition on the Orbitrap Elite and Orbitrap Fusion Lumos.

153 lial cells is mediated by the conserved core fusion machinery, composed of the fusogen gB and the rec

154 te Ca(2+) activation of the synaptic vesicle fusion machinery.

155 -terminal in-frame green fluorescent protein fusion may slow down the proteasome-mediated proteolysis

156 y eukaryotic organisms share a common gamete fusion mechanism.

157 y that is required for efficient ER membrane fusion mediated by RHD3.

158 monstrating that MLL1 is dispensable for MLL-fusion-mediated leukemogenesis.

159 A novel sample fusion method is developed, tested, and validated to pro

160 n were rapidly isolated and deposited from a fusion mixture as single-cell clones via FACS.

161 a rhodopsin (Rho)-guanylyl cyclase (GC) gene fusion molecule that is central to zoospore phototaxis i

162 The membrane fusion necessary for vesicle trafficking is driven by th

163 3 null mice represent a novel mouse model of fusion-negative RMS.

164 We demonstrate the application of our gene fusion neoantigen discovery pipeline, called INTEGRATE-N

165 inhibit autophagosome formation or block the fusion of autophagosomes to endolysosomal compartments c

166 lar processes, including endosome formation, fusion of autophagosomes/amphisomes with lysosomes, and

167 ing film-coupled nanocubes in pixels using a fusion of bottom-up and top-down fabrication techniques

168 cC interacts with other cellular Cdks, but a fusion of CycC to Cdk8 reported here did not cause any o

169 T2 activity in HEK293T cells with an mCherry fusion of EGFP-K85AcK, and showed that this approach can

170 In-frame fusion of green fluorescent protein (GFP) to the C-termi

171 This Ca(2+) release triggered the fusion of lysosomes with the plasma membrane, resulting

172 x differentiation process that culminates in fusion of mononuclear osteoclast precursors.

173 Skeletal muscle development requires fusion of mononuclear progenitors to form multinucleated

174 Vacuole generation involved the homotypic fusion of Munc13-4(+)/Rab7(+) SGs, followed by a merge w

175 ated skeletal muscle fibers form through the fusion of myoblasts during development and regeneration.

176 ll as triggered lamellipodia, spreading, and fusion of myoblasts through the signaling function of th

177 Gm7325, which we name myomerger, induces the fusion of myomaker-expressing fibroblasts.

178 inally, reintroduction of linoleic acid, via fusion of phospholipid vesicles to mitochondria isolated

179 g the hyperfusogenic form of gB may regulate fusion of PILRalpha via a novel mechanism through gH/gL

180 ls that the unitary chromosome arose through fusion of six ancestral chromosomes, with extensive rear

181 ssion of Ihh, leading to abnormal phalanges, fusion of sutures and syndactyly.

182 unnels, which are formed by contact and self-fusion of the apical and basal plasma membranes.

183 es are entirely covered over by a continuous fusion of the cuticle, and consequently plants have decr

184 process that involves sequential growth and fusion of the facial prominences.

185 ancers, chromosomal rearrangements cause the fusion of the promoter and 5'-UTR of the androgen-regula

186 riments revealed that LY6E promotes membrane fusion of the viral entry step.

187 from P. putida reveals that the protein is a fusion of two distinct modules: an N-terminal sugar phos

188 in which the highly exothermic nature of the fusion of two heavy-quark baryons might manifest itself.

189 Munc13-4 promoted the Ca(2+)-stimulated fusion of VAMP8-containing liposomes with liposomes cont

190 he cellular SNARE system, which mediates the fusion of vesicles in healthy cells, and its relation to

191 We expressed fluorescent fusions of FtsZ from diverse photosynthetic organisms in

192 The prevalence of fusions of the transmembrane protease, serine 2, gene (T

193 We demonstrate IM-Fusion on two separate transposon screens of 123 mammary

194 mino acids at C-terminus does not promote LD fusion or TAG accumulation, while it still localizes to

195 her repeated in the same location (two-flash fusion) or moved in space (apparent motion).

196 Comparison of SPOP-mutant and ERG-fusion organoid models showed evidence of divergent, rat

197 cations focused on 186 key genes and 286 key fusion pairs across all cancers.

198 Agena LungFusion panel and ThermoFisher NGS fusion panel) to those obtained from ALK, ROS1 and RET F

199 r group revealed the presence of PDGFRB gene fusions, particularly EBF1-PDGFRB, in almost one third o

200 e demonstrate the versatility of HUH-tags as fusion partners in Cas9-mediated gene editing and the co

201 scoidal nanolipoprotein particles (vNLPs) as fusion partners with cells ectopically expressing cognat

202 gnostic of particular sarcoma types, certain fusion partners, most notably EWSR1, are not tumor speci

203 The exact location of the CoV fusion peptide (FP) has been disputed.

204 Phagosome-with-lysosome fusion (PLF) results in the delivery of lysosomal hydrol

205 assays show a strain-independent failure of fusion pore enlargement among H2 (A/Japan/305/57), H3 (A

206 tion of the plasma membrane might facilitate fusion pore formation during exocytosis.

207 se indicate that G100V/C103V retards initial fusion-pore opening, hinders its expansion and leads to

208 sence of Nef inhibits the formation of small fusion pores between viruses and cells.

209 are released through fluctuating exocytotic fusion pores that can flicker open and shut multiple tim

210 Here, we probed the dilation of single fusion pores using v-SNARE-reconstituted 23-nm-diameter

211 rify that this affects the morphology of the fusion product and regulates transporter protein degrada

212 easier by automating the annotation of gene fusion products and generating easily interpretable visu

213 IV5 was engineered to express either the RSV fusion protein (F) or the RSV major attachment glycoprot

214 We have generated a hexameric-Fc fusion protein (hexameric-Fc) and tested the consequence

215 sses of EPIs that interact with the membrane fusion protein AcrA, a critical component of the AcrAB-T

216 5;17) translocation generates a PML-RARalpha fusion protein causative for acute promyelocytic leukemi

217 support further evaluations of pretargeting fusion protein cocktails as a strategy to enhance nanopa

218 vivo by Mef2c-Dam adenine methyltransferase fusion protein confirmed the link between cognitive enha

219 that immune responses to the more conserved fusion protein contribute to protection against heterolo

220 Finally, we present a workflow for fusion protein design and discuss best practices for eng

221 tial order of allergen and adjuvant within a fusion protein determines its immunologic characteristic

222 y captured by an immobilized SpyCatcher-SrtA fusion protein during purification.

223 inal fusions, this virus expresses more VP26 fusion protein in infected cells and incorporates more V

224 n fluorescent protein [eGFP]) or an NSs-eGFP fusion protein in the NSs locus.

225 in infected cells and incorporates more VP26 fusion protein into virus particles, and individual viru

226 rs show that a chemical inhibitor to a viral fusion protein is effective in reducing viral titre and

227 d Dusp1 suppressed tumor growth in a BCR-ABL fusion protein kinase-induced mouse model of chronic mye

228 ate that expression of either the endogenous fusion protein or a chimeric cDNA leads to the formation

229 We used a soluble IN fusion protein to facilitate structural studies, through

230 the BAF complex is recruited by the EWS-FLI1 fusion protein to tumor-specific enhancers and contribut

231 AtHEMN1-green fluorescent protein fusion protein was found targeted to mitochondria.

232 have minimal impact on the properties of the fusion protein, as they have no propensity to form order

233 es of the Fas death receptor, the HIV-1 gp41 fusion protein, the influenza proton channel, and the MC

234 re metastases, than cells not expressing the fusion protein.

235 ne AML model driven by the MLL-AF9 oncogenic fusion protein.

236 glutide, a glucagon-like peptide 1 (GLP1)-Fc fusion protein.

237 egulated when co-expressed with the J-domain fusion protein.

238 refusion and postfusion conformations of the fusion protein.IMPORTANCE Due to lapses in vaccination w

239 Paramyxovirus viral fusion proteins (F) insert into the target cell membrane

240 cells, we engineered CD200R immunomodulatory fusion proteins (IFPs) with the cytoplasmic tail replace

241 To investigate the interplay of fusion proteins and microenvironment in lineage choice,

242 As therapeutic recombinant fusion proteins become more widely applicable for the tr

243 Such fusion proteins can enhance the efficacy of allergen-spe

244 BAR-domain proteins such as the fusion proteins Fus2p and Rvs161p are known to recognize

245 Chimeric antigen receptors (CARs) are fusion proteins incorporating antigen-recognition domain

246 single-protein convenience of integrase-RDF fusion proteins make them potentially very advantageous

247 ji and Jurkat tumors, pretargeting with both fusion proteins markedly increased nanoparticle targetin

248 We sought to characterize different fusion proteins of flagellin and the major birch pollen

249 we tested whether immunoregulatory cytokine fusion proteins of IL-10/Fc, TGF-beta/Fc, or IL-2/Fc wou

250 Fusion proteins scFvFITC:sTRAIL and scFvFITC:sFasL induc

251 that this spatiotemporal association of the fusion proteins selectively alters the methylation state

252 or genome targeting with Fkbp/Frb dimerizing fusion proteins to allow chemical-induced proximity of a

253 D-L1 antibodies, OX40 ligand, or GITR ligand fusion proteins, produced synergistic antitumor response

254 mixed-lineage leukemia gene (MLL) create MLL-fusion proteins, which could drive both acute lymphoblas

255 t reveal homology to class II viral membrane fusion proteins.

256 chromosomal translocations that create novel fusion proteins.

257 ctron poor units facilitates a visible light fusion reaction in >95% yield, whereas the cove-edge nat

258 s for the first wall/blanket applications in fusion reactor.

259 rge of the lysine residues was necessary for fusion regulation, as alanine substitutions induced a 44

260 the transmembrane domains (TMDs) in membrane fusion remains controversial.

261 ether crossover formation actually energizes fusion remains unclear, as do the sequence of events sur

262 the host receptor and in mediating membrane fusion, respectively.

263 apable of pH-induced triggering for membrane fusion, resulting in lysosomal degradation.

264 o localization of AtCPT7 fluorescent protein fusions showed that AtCPT7 resides in the stroma of meso

265 Fluorescent reporter fusions showed that SLI1 is confined to the margins of s

266 tages over strategies based on liquid phase (fusion) sintering that requires both oxide-free metal su

267 and partially colocalize at the presumptive fusion site.

268 pects of correlative image overlay and image fusion specific to SIMS-based correlative microscopy are

269 is important for F protein function and pre-fusion stability.

270 e elements that control stability of the pre-fusion state and triggering to the post-fusion conformat

271 racterized viruses expressing amino-terminal fusions, this virus expresses more VP26 fusion protein i

272 (2+) release channel P2X4 regulates lysosome fusion through a calmodulin (CaM)-dependent mechanism.

273 y conserved Rho-GTPase Cdc42p promotes yeast fusion through interaction with Fus2p, a pheromone-induc

274 In contrast, patients with FGFR1 and JAK2 fusion TK genes exhibit a more aggressive course and var

275 ound that hyperfusogenic gB mutants enhanced fusion to a greater degree with the gB receptor the pair

276 vesicle fusion and used it to study vesicle fusion to a tethered lipid bilayer.

277 ciples such as focus+context and visual data fusion to enable users to better understand the statisti

278 This pathway may link outer membrane fusion to lipids homeostasis.

279 in which two heavy baryons (Lambdac) undergo fusion to produce the doubly charmed baryon and a neutro

280 arriers, however they often require covalent fusion to the protein for efficient delivery.

281 as a stand-alone protein or as an N-terminal fusion to the respective RS enzyme.

282 ghlighting a distinct responsiveness of CRAF fusions to clinically relevant RAFi.

283 Fluorescent protein fusions to the amino terminus of small capsid protein VP

284 uss the molecular mechanisms that link these fusions to the control of cell death.

285 Consequently, such specific fusion toxin proteins could form the basis of a therapeu

286 method, ChimeRScope that accurately predicts fusion transcripts based on the gene fingerprint (as k-m

287 AREs, and that this assembly undergoes rapid fusion upon addition of Qb and Sec17.

288 rf-like GTPase 8) and its effector homotypic fusion/vacuole protein sorting complex (HOPS) to (phago)

289 In this study, gBcyt-regulated fusion was investigated by comparing melanoma cells infe

290 nd events (i.e. granule-to-granule homotypic fusion) was severely reduced in the absence of Munc13-4.

291 Here, using a translational gene fusion, we show that CrsR sequesters and protects sigma(

292 ancy characterized by expression of SS18-SSX fusions, where treatment options are limited.

293 mation of the ER requires homotypic membrane fusion, which is mediated by a family of Dynamin-like At

294 We expect that IM-Fusion will significantly enhance the accuracy of cancer

295 cell wall deposition within 30 seconds after fusion with a sperm [3], thereby preventing further fert

296 The vesicle uncoats before fusion with a target membrane.

297 The binding properties of 40 CBMs, in fusion with an N-terminal GFP domain, revealed that type

298 tibodies, CL40 and CL59, that block membrane fusion with both B cells and epithelial cells.

299 if that is necessary for promoting cell-cell fusion with myomaker.

300 te that neuronal activity triggers lysosomal fusion with the plasma membrane in dendrites.