ライフサイエンスコーパス: surface protein

1 ocytosis, likely with the help of a cellular surface protein.

2 cell progenitor cells to Abs targeted to 176 surface proteins.

3 -glycosylated sites were quantified from 168 surface proteins.

4 sured 2D Kd values for interacting leukocyte surface proteins.

5 e characterized by upregulation of bacterial surface proteins.

6 nctions with equal efficiencies and ingested surface proteins.

7 eased membrane levels of integrins and other surface proteins.

8 ion with other extracellular matrix and cell surface proteins.

9 urface receptors whose ligands are also cell surface proteins.

10 o manipulate viral tropism by swapping viral surface proteins.

11 nds often presented in large numbers as cell surface proteins.

12 ntrolled by the concentration of immobilized surface proteins.

13 n shedding of metalloprotease-sensitive cell surface proteins.

14 ased directed movement of a subset of apical surface proteins.

15 the downregulation of a broad range of cell-surface proteins.

16 wing proteinase K-mediated clearance of cell-surface proteins.

17 L-4 and analyzed for expression of >300 cell-surface proteins.

18 luding lipooligosaccharide glycans and outer surface proteins.

19 that regulate endosomal trafficking of cell surface proteins.

20 s able to recognize and degrade damaged cell surface proteins.

21 that it lacks the "LPXTG" motif for typical surface proteins.

22 2, NOTCH2 and FLT3, that encode myeloid cell surface proteins.

23 es targeting conserved elements on influenza surface proteins.

24 ling medical devices using a variety of cell-surface proteins.

25 es of interactions between host and parasite surface proteins.

26 the C-terminal 19-kDa fragment of merozoite surface protein 1 (MSP119) to P. falciparum MSP8 (PfMSP8

27 rom Mozambique: 19-kDa fragment of merozoite surface protein 1 (MSP119), erythrocyte binding antigen

28 he 19 kDa fragment of the P. vivax Merozoite Surface Protein 1 (PvMSP119) is one of the most promisin

29 at antibodies to 5 proteins of the Merozoite Surface Protein 1 complex were differentially acquired b

30 tem by targeting the P. falciparum merozoite surface protein 1 gene (msp1), which has previously prov

31 ly variable region of the P. vivax merozoite surface protein 1 gene revealed impressive diversity-gen

32 e circumsporozoite protein and the merozoite surface protein 1.

33 redominately via C1q fixation, and merozoite surface proteins 1 and 2 were identified as major target

34 a major invasion-related protein, merozoite surface protein-1 (MSP-1).

35 -1, apical membrane antigen-1, and merozoite surface protein-1 do not to predict protection from chal

36 notyping of the highly polymorphic merozoite surface protein 2 gene was performed on blood samples co

37 entified PfMSP3.1, a member of the merozoite surface protein 3 family of merozoite surface proteins,

38 Merozoite surface protein 3 of Plasmodium falciparum, a 40-kDa pro

39 antibody-drug conjugates targeting the cell surface protein 6 transmembrane epithelial antigen of pr

40 d on the use of highly immunogenic merozoite surface protein 8 (MSP8) as a vaccine carrier protein.

41 Neisserial surface protein A (NspA) is a highly conserved outer mem

42 Outer surface protein A (OspA) coats the spirochetes from the

43 m concentrations of antibodies against outer surface protein A (OspA) were shown to correlate with pr

44 eta/alpha-sandwich) and another within outer surface protein A (OspA, beta-sheet) to have high sequen

45 e virulence-associated proteins pneumococcal surface protein A (PspA) and pneumococcal choline-bindin

46 nosensor for rapid detection of pneumococcal surface protein A (PspA) peptide and SP lysate from synt

47 In that regard, pneumococcal surface protein A (PspA), a major surface protein of pne

48 triad proteins (PhtD and PhtE), pneumococcal surface protein A (PspA), plasminogen and fibronectin bi

49 nce for the antigenic region of pneumococcal surface protein A (PspA).

50 on humoral memory responses to pneumococcal surface protein A (PspA).

51 nce for the antigenic region of pneumococcal surface protein A and demonstrated that mice immunized w

52 y S. pneumoniae lacking the CBP pneumococcal surface protein A lost its ability to inhibit the IgG an

53 cence assays that combined monoclonal (outer surface protein A) and polyclonal antibodies were perfor

54 ded 109 variants of the diverse pneumococcal surface proteins A and C (PspA and PspC) and zinc metall

55 These outputs included an immunogenic cell-surface protein, a cytokine, a chemokine, and a checkpoi

56 Interestingly, FACIN is a nonclassical cell surface protein, a cytosolic enzyme acetylornithine tran

57 COMP interacts directly with the ubiquitous surface protein A2 of M. catarrhalis.

58 49) through interaction with the ubiquitous surface protein A2/A2H.

59 These viral surface proteins act as the primary interface between th

60 phospholipases C (PLCs; PlcA and PlcB) and a surface protein (ActA).

61 er specific to 8 group B Streptococcus (GBS) surface proteins among 81 HIV-uninfected and 83 HIV-infe

62 tein (APP) is an ubiquitously expressed cell surface protein and a key molecule in the etiology of Al

63 We show that Z2 interacts with ZIKV surface protein and disrupts the integrity of the viral

64 Cell surface protein and lipid molecules are organized in var

65 red from US strains by acquisition of a cell-surface protein and macrolide resistance determinants vi

66 pecific and stronger binding between exosome surface protein and the aptamer displaces aptamers from

67 ted in the late 1970s by acquisition of cell surface proteins and antimicrobial resistance determinan

68 er surface proteins in adhesion to host cell surface proteins and extracellular matrix components, al

69 host cuticle led to a selective radiation of surface proteins and hydrolytic enzymes.

70 th antibodies to enable profiling of exosome surface proteins and proteins present in exosome lysates

71 om our initial analysis of 62 B. burgdorferi surface proteins and synthetic peptides by assessing bin

72 etry was used to evaluate expression of cell-surface proteins and the cytokine production profile of

73 antibodies that are specific to tumour cell-surface proteins and, thus, have tumour specificity and

74 M protein is the most abundant GAS surface protein, and M1 serotype GAS strains are associa

75 proteins regulate Eph/ephrins and other cell-surface proteins, and can function in a non-cell-autonom

76 es encoding toxins, adhesins, and other cell surface proteins, and over 200 BtrA-repressed genes that

77 ellular adhesin (PIA) and extracellular DNA, surface proteins appear to mediate the transition of bac

78 We found that while specific S. aureus surface proteins are a prerequisite for agglomeration in

79 rtebrate clustered protocadherin (Pcdh) cell surface proteins are encoded by three closely linked gen

80 Glycosylation alterations of cell surface proteins are often observed during the progressi

81 geted biocarrier that exploits the HER3 cell surface protein as a portal to sneak therapeutics into t

82 ber of the six-cysteine family of Plasmodium surface proteins, as its direct interaction partner.

83 ozoite surface protein 3 family of merozoite surface proteins, as the direct interaction partner.

84 host entry factors, such as CD81, a key cell surface protein associated with HCV entry.

85 BST-2 co-localized with HBV surface protein at multivesicular bodies (MVBs) and phys

86 s is dependent upon the display of bacterial surface proteins attached to the cell wall by the B. ant

87 through its interaction with the erythrocyte surface protein basigin (also known as CD147 and EMMPRIN

88 processes require dynamic modulation of cell surface proteins by endocytosis.

89 flammatory dermatoses were analyzed for cell surface proteins by flow cytometry and for copy number a

90 re we report comprehensive profiling of cell surface proteins by flow cytometry in naive and primed h

91 The frequent modification of cell-surface proteins by N-linked glycans is known to be corr

92 Outer surface protein C (OspC) is one of the major lipoprotein

93 d virulence factor B (PavB) and pneumococcal surface protein C (PspC) are key players for the interac

94 with low titers against group 3 pneumococcal surface protein C (PspC) variants were more likely to be

95 Here, we identify new roles for two apical surface proteins - Cadherin 99C (Cad99C) and Stranded at

96 Gram-positive surface proteins can be covalently or non-covalently anc

97 Antibodies against viral surface proteins can blunt the spread of viral infection

98 Here, we demonstrate that the cell-surface protein CD276/B7-H3 is broadly overexpressed by

99 sis is normally inhibited by binding of cell surface protein CD47 to macrophage signal regulatory pro

100 quitously express the immunosuppressive cell surface protein CD80 (B7-1).

101 modium vivax, rely on two distinct host cell surface proteins, CD81 and the Scavenger Receptor BI (SR

102 ired PanNETs characterized by increased cell-surface protein CD90 expression and aldehyde dehydrogena

103 Antibody-induced shedding of the major surface protein circumsporozoite protein (CSP) exposed t

104 Expression of the surface protein Cnm has been directly implicated in the

105 te that Reck and Gpr124 are part of the cell surface protein complex that transduces Wnt7a- and Wnt7b

106 nd further characterized the major merozoite surface protein complex.

107 lish LD identity by defining positioning and surface-protein composition.

108 y particle size, emulsifying activity index, surface protein concentration at the interface and by tr

109 However, the molecular mechanisms by which surface proteins contribute to biofilm formation are inc

110 Bacterial surface proteins covalently attach to host cells via a m

111 Here we show that the conserved cell-surface protein CwpV provides antiphage protection in C.

112 . also identify the unique expression of the surface protein DC-HIL on psoriatic Mo-MDSC.

113 n, the last step of endocytosis required for surface protein degradation.

114 have identified a unique mouse Pneumocystis surface protein, designated Pneumocystis cross-reactive

115 -structural protein NS1, rather than a viral surface protein, determines IEC tropism.

116 However, specific charge modification of surface proteins did not change cell migration motility

117 st, sortase A mutants, which cannot assemble surface proteins, display delayed time to death and incr

118 nds for apical membrane antigen (AMA) family surface proteins displayed on the parasite.

119 ry-triggering protein to bind the human cell surface protein DNase X.

120 enefit their survival, and the study of cell surface proteins downregulated by viruses has provided i

121 usual members of the MSP-3 family, merozoite surface protein duffy binding-like (MSPDBL)1 and MSPDBL2

122 The upregulation of naive-specific cell surface proteins during primed-to-naive resetting enable

123 Expression analysis of >300 surface proteins enabled identification of IL-4-upregula

124 enes are evolving at higher rates than other surface protein-encoding genes.

125 etabolic pathways, but contain expansions of surface proteins, especially a unique and complex surfac

126 argets ROR1, which encodes an onco-embryonic surface protein expressed on the CLL cells of over 90% o

127 unoglobulin-like lectin (Siglec)-8 is a cell-surface protein expressed selectively on human eosinophi

128 To identify and characterize surface proteins expressed by the relapsing fever (RF) a

129 especially on the roles of secreted and cell surface proteins, expressed in a sex-specific manner, th

130 The CD133 cell-surface protein expresses the AC133 epitope that is asso

131 TNFRSF13C, which are bound by HuR, increase surface protein expression compared to their correspondi

132 analysis approach to evaluate heterogeneous surface protein expression in single circulating exosome

133 DLL3, although orders of magnitude lower in surface protein expression than typical oncology targets

134 Moreover, IL-33 increases NK-1 gene and surface protein expression, as well as IKbeta-alpha phos

135 urrent density without perturbing Kv4.3 cell surface protein expression.

136 astric tissue samples were analyzed for cell surface protein expression.

137 ell understood because of the number of cell surface proteins, factors, and conditions found to be as

138 hese parasites have evolved specialized cell-surface protein families, overlaid on a well-conserved c

139 This highlights the extent to which such a surface protein family can diversify while maintaining l

140 ence are mediated by the parasite-derived IE surface protein family Plasmodium falciparum erythrocyte

141 , and ess extracellular B (EsxB) and the two surface proteins ferric hydroxamate uptake D2 and conser

142 We screened Leptospira outer membrane/surface proteins for their ability to activate/inhibit T

143 ites on Fn-binding protein A (FnBPA), a cell surface protein from Staphylococcus aureus, are implicat

144 molecular and structural study of the major surface proteins from an A(H3N8) influenza virus isolate

145 prevaccination concentrations of IL-10 (RV5 surface proteins G1 and P1) and IFNgamma (G1) in the HIV

146 In this study, the FbaA surface protein gene was found to be present in most ski

147 ental contributions to fitness of individual surface protein genes and the multifactorial nature of G

148 erves as an essential chaperone for the cell-surface protein glycoprotein A repetitions predominant (

149 Antibody directed against the viral surface protein glycoprotein B functionalized with gluco

150 The EBV surface protein gp350 is a major target for antibodies.

151 that the glycophosphatidylinositol-anchored surface protein GPI-80 defines a subpopulation of human

152 s, the antibody-binding domains of the viral surface protein haemagglutinin.

153 can be found in gram-positive bacterial cell surface proteins, has previously been used to develop a

154 In particular, streptococcal surface proteins have been implicated as potent neutroph

155 uenza A(H3N2) virus based on the sequence of surface protein hemagglutinin (HA).

156 between the functions of the influenza virus surface proteins hemagglutinin (HA) and neuraminidase (N

157 between the functions of the influenza virus surface proteins hemagglutinin (HA) and neuraminidase (N

158 an in-house database of genes encoding cell surface proteins (herein referred to as the surfaceome)

159 entry mediator (HVEM) is one of several cell surface proteins herpes simplex virus (HSV) uses for att

160 Using conserved surface proteins highly expressed during virulent transi

161 arum circumsporozoite protein (CSP), a major surface protein implicated in the structural strength, m

162 Neuropilins are a class of cell surface proteins implicated in cell migration and angiog

163 we report synthesis of core-shell structured surface protein-imprinted nanoparticles with reversible

164 chanism driving polar localization of a cell surface protein in plants.

165 ibing the roles of many B. burgdorferi outer surface proteins in adhesion to host cell surface protei

166 Surface proteins in all vertebrate HBVs contain similar

167 ggest the importance of lateral diffusion of surface proteins in contributing to a gradual increase i

168 sporozoite surface proteome and the roles of surface proteins in distinct biological activities of sp

169 ceptors belong to the largest family of cell surface proteins in eukaryotes, the G protein-coupled re

170 Surface proteins in Gram-positive bacteria are incorpora

171 port a sensor platform that profiles exosome surface proteins in minutes by the naked eye.

172 cal basis for molecular recognition of viral surface proteins in order to build predictive molecular

173 mined whether beta-1,3-glucans are masked by surface proteins in Pneumocystis and what role beta-gluc

174 enia are likely to be those directed to cell surface proteins, in which the likelihood of pathogenici

175 sma membrane via interaction with other cell surface proteins including glycosylphosphatidylinositol-

176 and induced a set of immune-suppressive cell-surface proteins, including BTLA, IRF4, and Siglec G.

177 metalloprotease ADAM10 sheds a range of cell surface proteins, including ligands and receptors of the

178 ch catalyzes transpeptidation reactions.1, 2 Surface proteins, including virulence factors, that have

179 Two interacting pairs of cell surface proteins independently promote fasciculation bet

180 study, we show that Abs against cancer cell surface proteins induce complement-dependent cytolysis o

181 actions among pancreatic beta-cells via cell surface proteins inhibit basal and enhance stimulated in

182 mediated by the interaction of two bacterial surface proteins, InlA and InlB, with their respective r

183 ted endocytosis is a major regulator of cell-surface protein internalization.

184 fe cycle and a complex array of co-expressed surface proteins involved in host cell binding.

185 on toxicity; (iii) higher expression of cell surface proteins involved in immune evasion and stress r

186 n leukocyte antigen (HLA) system encode cell-surface proteins involved in regulation of immune respon

187 erium displays a set of virulence-associated surface proteins involved in the interaction with the ho

188 on to the F fusion protein, the G attachment surface protein is a target for neutralizing antibodies

189 Endocytic down-regulation of cell-surface proteins is a fundamental cellular process for c

190 Aberrant glycosylation on surface proteins is associated with different cellular s

191 The PfEMP1 family of surface proteins is central for Plasmodium falciparum vi

192 in to maintain ER homeostasis, and as a cell surface protein, is known to regulate the phosphatidylin

193 Immunogold labeling and surface protein isolation identified decreased plasma me

194 his study, we show that the Egr2-driven cell surface proteins LAG-3 and 4-1BB can identify dysfunctio

195 mily lectins or Siglecs are a family of cell surface proteins largely expressed in hematopoietic cell

196 sing a monoclonal antibody against a hepatic surface protein, leucine amino peptidase (LAP).

197 nding in ITGAM, we quantitated ITGAM RNA and surface protein levels in monocytes from patients with e

198 ies (BsAbs) is affected by the relative cell-surface protein levels of the respective targets.

199 provide phenotypic information such as cell-surface protein levels.

200 Moreover, heme interaction with a surface protein like MSP3, which does not participate in

201 We compared GBS capsular and surface-protein maternal immunoglobin G antibody concent

202 In Gram-positive pathogens, surface proteins may be covalently anchored to the bacte

203 rferi harbors a limited set of transmembrane surface proteins, most of which constitute key targets o

204 ons between nanotubes and AMB-1 via the cell surface protein MSP-1 and flagellin.

205 um erythrocyte membrane protein 1, merozoite surface protein (MSP) 10, MSP2, liver-stage antigen 3, P

206 odel with T cells specific for the merozoite surface protein (MSP)-1 of Plasmodium chabaudi to show t

207 dium falciparum, genotyping of the merozoite surface protein (MSP1/2) genes is a standard method for

208 The most abundant merozoite surface protein, MSP1, is synthesized as a large precurs

209 We have shown that the peripheral merozoite surface proteins MSPDBL1 and MSPDBL2 are part of the lar

210 e suggests that antibodies against merozoite surface proteins (MSPs) play an important role in clinic

211 aining the scaffold protein and deficient in surface proteins needed for cell entry.

212 eumococcal surface protein A (PspA), a major surface protein of pneumococci, is a promising vaccine t

213 SasX is a recently described surface protein of Staphylococcus aureus that is linked

214 transmembrane protein 119 (Tmem119), a cell-surface protein of unknown function, as a highly express

215 d eastern equine encephalitis expressing the surface proteins of all three viruses.

216 strate this novel approach by characterizing surface proteins of different cell types at the single-c

217 Neuraminidase (NA) is one of the major surface proteins of influenza virus, serving as an impor

218 Two surface proteins of P. gingivalis, PGN_0294 and PGN_0806

219 ple preparation technique to enrich for cell surface proteins of the intrahepatic cholangiocarcinoma

220 es, in which loci that encode immunodominant surface proteins (ompA and pmpEFGH) have been replaced b

221 mAbs specific for surface proteins on APCs can serve as Ag-delivery vehicl

222 bodies to target functionally important cell-surface proteins on bone-resorbing osteoclasts represent

223 Biotin labeling of surface proteins on infected cells indicated that only h

224 environment and influence S-nitrosylation of surface proteins on platelets and endothelial cells.

225 ost-microbe interface that involve microbial surface proteins, or adhesins.

226 lular adhesion molecule 1 (ICAM-1) is a cell-surface protein overexpressed in many diseases and explo

227 in a majority of the animals, antibodies to surface proteins persisted beyond the duration of the st

228 rphism in the Plasmodium gene coding for the surface protein Pfs47 modulates resistance of some paras

229 Hic, a PspC-like pneumococcal surface protein, possesses vitronectin and factor H bind

230 transporters are a large superfamily of cell surface proteins produced by Gram-negative bacteria that

231 of techniques for the detection of reactive surfaces, protein-protein docking and molecular simulati

232 Assessing exosome surface proteins provides a powerful means of identifyin

233 seases; they arise from misfolding of a cell surface protein, PrP(C) to a form called PrP(Sc).

234 Isolation of the streptococcal surface proteins recognised by pooled human immunoglobul

235 T, and NK cells may modulate the function of surface proteins recognized by natural or immune IgM Abs

236 ceptors, one of the largest families of cell surface proteins, representing a major class of drug tar

237 charomyces pombe shu1(+) gene encodes a cell-surface protein required for assimilation of exogenous h

238 ers (Pra1 and Zrt1) and other zinc-regulated surface proteins, resulted in lower autoaggregation and

239 of the extracellular matrix as well as cell surface proteins resulting in degradation or release of

240 Isolation of surface proteins revealed higher amounts of alpha4 or be

241 coding the transcription factor repressor of surface proteins (rsp).

242 PagM promotes group motility by a surface protein(s), as a pagM-expressing strain conferre

243 Staphylococcus aureus surface protein SasG promotes cell-cell adhesion during

244 We examined the ability of the surface protein SdrF to adhere to keratin, a major molec

245 neumococci express a versatile repertoire of surface proteins sequestering and interacting specifical

246 Here we show that the streptococcal surface protein SfbI mediates covalent interaction with

247 Biotinylating platelet surface proteins showed ADAMDEC1 hydrolyzed surface pro-

248 Exosomes contain surface proteins, some of which can act as labels in ord

249 e characterize a novel, conserved sporozoite surface protein (SSP3) in the rodent malaria parasite Pl

250 s enabled identification of IL-4-upregulated surface proteins, such as CD90, CD108, CD109, and CD200R

251 at mutations accumulate in epitopes of viral surface proteins, suggesting selection for immune escape

252 We aimed to identify novel cell surface proteins targeted for downregulation by HIV-1.

253 primary tumors, and showed that CD47, a cell-surface protein that acts as a "don't eat me" signal co-

254 - gestation mouse placenta as well as a cell surface protein that can be used to identify and isolate

255 Here, we identify P113 as a merozoite surface protein that directly interacts with RH5Nt.

256 ression of staphylococcus protein A (SpA), a surface protein that drives polyclonal B cell expansion

257 eceptor (FLVCR) is a 12-transmembrane domain surface protein that exports heme from cells, and it was

258 2 (NL2), an inhibitory synapse-specific cell surface protein that functions in cell adhesion and syna

259 accine development, Pfs25, is a sexual stage surface protein that has been produced for vaccine testi

260 CD38 is a multifunctional cell surface protein that has receptor as well as enzyme func

261 ific angiogenesis inhibitor (BAI3) as a cell surface protein that interacts with ELMO.

262 In this study, we show that THY-1, a cell surface protein that is critical for the early stage of

263 tine/glutamate antiporter system xc(-), as a surface protein that is upregulated specifically in tumo

264 nduce the formation of antibodies to a viral surface protein that neutralize the infectivity of the v

265 CD47 is a cell surface protein that transmits an anti-phagocytic signal

266 ted via a range of strain-specific bacterial surface proteins that bind to a variety of platelet rece

267 and viral decoys, including challenging cell surface proteins that cannot be produced using typical d

268 tive bacteria, anchors on the cell wall many surface proteins that facilitate bacterial pathogenesis

269 Ephrins are cell surface proteins that regulate diverse biological proces

270 rearrangement and crosslinking of the viral surface proteins that result in neutralization.

271 heating was developed to perform a rapid on-surface protein thermal decomposition and digestion suit

272 Bacteria exploit surface proteins to adhere to other bacteria, surfaces a

273 ells, VZV alters cell signaling and remodels surface proteins to enhance T cell skin trafficking.

274 P1 interacts with other peripheral merozoite surface proteins to form a large complex.

275 Pathogens use a variety of secreted and surface proteins to interact with and manipulate their h

276 Enveloped viruses employ specialized surface proteins to mediate fusion of cellular and viral

277 ere, we defined the contributions of the Prg surface proteins to plasmid transfer, biofilm formation

278 It requires parasite surface proteins to provide attachment to host cells and

279 zed epithelial cells, newly synthesized cell surface proteins travel in carrier vesicles from the tra

280 IV-1 spread; critically, however, which cell surface protein triggers contact-induced polarization at

281 us infects cells when the hemagglutinin (HA) surface protein undergoes irreversible pH-induced confor

282 t did not affect osteogenesis, adipogenesis, surface-protein unfolding or underlying substrate deform

283 uman immunization with a candidate merozoite surface-protein vaccine.

284 sor, cystatin, and numerous Variant-specific Surface Proteins (VSPs).

285 ce conservation of the core, polymerase, and surface proteins was low and ranged from 16 to 27% at th

286 thod of limited proteolysis of lipid droplet surface proteins, we found that the C terminus of Tgl3p

287 lular biotin acceptor tag to directly assess surface proteins, we observed significant PDZ ligand-dep

288 emonstrated that many glycosylation sites on surface proteins were down-regulated in statin-treated c

289 Cell surface proteins were quantified by flow cytometry.

290 n mechanics and adhesion in a staphylococcal surface protein, which may represent a general mechanism

291 ing pilus structures, along with other LPXTG surface proteins, which are processed by sortases upon s

292 gnify a large family of structurally related surface proteins, which contribute to the ability of str

293 llate a set of AS and DE genes encoding cell surface proteins, which present promising diagnostic and

294 only conferred by the interaction of a viral surface protein with a host receptor complex.

295 glycosylphosphatidylinositol (GPI)-anchored surface protein with a modified eight-cysteine motif (M8

296 Thy1 (CD90), a cell surface protein with an enigmatic function, is expressed

297 eaction involves ClfA (clumping factor A), a surface protein with serine-aspartate (SD) repeats that

298 reviously reported, interaction of S. aureus surface proteins with host matrix proteins such as fibri

299 gregation factor A (CafA), is one of 14 cell surface proteins with the LPXTG motif predicted in A. or

300 o monitor fluorescent ligand binding on cell-surface proteins with time-resolved Forster resonance en