ライフサイエンスコーパス: link protein

1 ct hyaladherins (aggrecan G1-NITEGE(373) and link proteins).

2 ntracellular scaffolding partner of this tip-link protein.

3 sulfate proteoglycans (CSPGs), aggrecan and link protein.

4 achinery, including the MET channels and tip-link proteins.

5 ands making multiple contacts with the cross-linked protein.

6 ar cyclization and a high yield of the cross-linked protein.

7 mor cells as a glycosyl-phosphatidylinositol-linked protein.

8 ross-linking sites are adjacent in the cross-linked protein.

9 dimers in the membrane by analysis of cross-linked proteins.

10 conjugation to visualize and identify cross-linked proteins.

11 oponin and exposed to UV light to form cross-linked proteins.

12 implicated in the processing of other ataxia-linked proteins.

13 keys, give rise to efficiently processed GPI-linked proteins.

14 g ortholog partners in pairs of functionally linked proteins.

15 luble structure composed of covalently cross-linked proteins.

16 ization, and interaction with itself and ALS-linked proteins.

17 ormed after enzymatic digestion of the cross-linked proteins.

18 raplakin, as a model actin-microtubule cross-linking protein.

19 hat differ in expression of this actin cross-linking protein.

20 ich is progressively stabilized by the cross-linking proteins.

21 V) and vascular stiffness, in part via cross-linking proteins.

22 otors and static forces from non-motor cross-linking proteins.

23 of plasma membrane-actin cytoskeleton cross-linking proteins.

24 band of cortical nodes and bundled by cross-linking proteins.

25 Cartilage Link Protein 1 (Crtl1) is an extracellular matrix (ECM)

26 approximately 200 genes, including cartilage link protein 1 (Crtl1).

27 n (HA), and link proteins, such as cartilage link protein 1 (Crtll).

28 inin alpha1, and hyaluronan and proteoglycan link protein 1 (Hapl1) production as well as proliferati

29 , we report that hyaluronan and proteoglycan link protein 1 (HAPLN1) is produced in bone marrow strom

30 oglycan versican/hyaluronan and proteoglycan link protein 1 rich myxoid matrix, which is in direct co

31 in, a vertebrate hyaluronan and proteoglycan link protein 1.

32 Hyaluronan-linked protein 1 (HAPLN1) which has been shown to be hig

33 de fluorogold labeling and brain-expressed X-linked protein-1/2 (Bex1/2) immunoreactivity.

34 It links protein 3D structure data with sequence data, sequ

35 inantly of the proteoglycan versican and its linking protein, a vertebrate hyaluronan and proteoglyca

36 ce of unbinding and unfolding of actin cross-linking proteins (ACPs) in the dynamic properties of the

37 aggregation of glycosylphosphatidylinositol-linked proteins activates Src-family kinases, the activa

38 n moieties are substituted for the thioester-linked protein acyl-modifications through a sequence of

39 We propose that O-linked protein ADPr is the key signal in PARP-1/PARP-2-d

40 e findings, we propose that 2 mechanisms may link protein aggregation and cardiac function: oligomer-

41 mutations in FHL1, thereby defining a new X-linked protein aggregation disorder of muscle.

42 olated raft fractions were enriched in a GPI-linked protein, alkaline phosphatase, and were poor in N

43 ciated proteins, isolation of the covalently linked proteins allows their identity to be assigned.

44 king is modulated by the Parkinson's disease-linked protein alpha-synuclein, but the contribution of

45 chizosaccharomyces pombe, in which the cross-linking protein alpha-actinin SpAin1 bundles the actin f

46 tin bundling by interacting with actin-cross-linking protein alpha-actinin-1 and increasing its affin

47 s, regulation of the homodimeric actin cross-linking protein alpha-actinin-4 (ACTN4) during cell migr

48 uscle cells contain the actin filament-cross-linking protein alpha-actinin.

49 egment, reminiscent of the Parkinson disease-linked protein, alpha-synuclein, which we show shares a

50 l peptide (LPP) is a proteolytic fragment of link protein, an important cross-linker and stabilizer o

51 We present a robust strategy to covalently link proteins and DNA using HUH-endonuclease domains as

52 M, integrates static and time series data to link proteins and the pathways they regulate in these ne

53 elin (HJV) is a glycosylphosphatidylinositol-linked protein and binds both bone morphogenic proteins

54 d layers, and produced lower levels of cross-linked protein and cornified envelopes.

55 p contains the virus-encoded proteins genome-linked protein and helper-component proteinase.

56 e that HJV is a glycosylphosphatidylinositol-linked protein and undergoes a partial autocatalytic cle

57 family of extracellular matrix receptors and linked proteins and discuss the evidence supporting thes

58 t significantly reduced association with ALS-linked proteins and inclusion into stress granules.

59 ope is assembled from transglutaminase cross-linked proteins and lipids in the outermost epidermal la

60 nding this method to the separation of lipid-linked proteins and transmembrane proteins while minimiz

61 l genomic analysis, we identify functionally linked proteins and verify their interaction in vitro by

62 These findings suggest roles for Lon in linking protein and mtDNA quality control.

63 aralog-specific behaviors of different cross-linking proteins and identify a zone of optimal actin-bi

64 cross-linking can also be applied for cross-linking proteins and phosphatidylethanolamine (PE).

65 tween the density of myosin motors and cross-linking proteins and the rigidity, initial orientation,

66 s a ubiquitously expressed enzyme that cross-links proteins and its overexpression, linked to a drug

67 lity to internalize bacterial exotoxins, GPI-linked proteins, and extracellular fluid.

68 of receptors, signal transducing kinases and linking proteins, and is responsible for the motile resp

69 ting of actin filaments, alpha-actinin cross-linking proteins, and non-muscle myosin IIA mini-filamen

70 aninum produces a family of small, disulfide-linked protein anticoagulants (75-84 amino acid residues

71 n the premise that hair cell stereocilia tip-link proteins are closely coupled with MET, these result

72 ll as the cognate kinase EnvZ, and the cross-linked proteins are capable of binding to DNA.

73 ific toxicity, despite the fact that disease-linked proteins are generally ubiquitously expressed.

74 esting the importance of incorrect disulfide-linked protein as key to MTSOD1 toxicity.

75 lioside GM1 and glycosylphosphatidylinositol-linked proteins as lipid raft markers.

76 ighly expressed genes encoding keratin cross-linking proteins associated with rumen evolution.

77 of actin filaments, myosin motors, and cross-linking proteins at biologically relevant time and lengt

78 ding with elevated expression of actin-cross-linking proteins at the neuronal growth cone, namely pho

79 n the central hydrophobic core and the cross-linked protein body periphery, respectively, but little

80 tructures contains actin filaments and cross-linking proteins, but the role of cross-linking proteins

81 The stereociliary link protein cadherin 23 (Cdh23) was targeted to the pla

82 The AP2 clathrin adaptor complex links protein cargo to the endocytic machinery but it is

83 pha-actinin-4 (Actn4), a dynamic actin cross-linking protein, cause proteinuric disease in humans and

84 to the carboxyl terminus of stereocilia tip-link protein CDH23 +68 (cadherin 23 with expressed exon

85 otein interaction for CNGA3 and a second tip-link protein, CDH23 +68, further suggests possible assoc

86 In this study, cartilage link protein (cLP) and the G1-domains of aggrecan (AG1)

87 stabilization of lipid microdomains by cross-linked protein clusters or ordered protein coats.

88 of genes in XXY female genotypes in which Y-linked protein-coding genes are not transcribed.

89 ene expression in XXY females in which the Y-linked protein-coding genes are not transcribed.

90 es of adaptive evolution for autosomal and X-linked protein-coding genes.

91 In addition, when cross-linked protein complexes are collisionally activated in

92 ubstrate pairs into stable, covalently cross-linked protein complexes, thereby facilitating their sub

93 We envision that disease-linked proteins confer stress on all relevant brain cell

94 ction of stable secondary and tertiary amine-linked protein conjugates without affecting the structur

95 flection generates a force by pulling on tip-link proteins connecting adjacent stereocilia.

96 Actin cross-linking proteins create a connected network from individ

97 riggered by neuronal production of cartilage link protein Crtl1 (Hapln1), which is up-regulated in th

98 Expression of the link protein Crtl1/Hapln1 in neurons has recently been i

99 of caveolin-3 and filamin (an F-actin cross-linking protein), decreased phosphorylation of caveolin-

100 vel regulators of endoplasmic reticulum (ER)-linked protein degradation and ER function, we determine

101 f proteomic pathway analysis to functionally link proteins differentially expressed in bone and skin

102 Disulfide-linked protein-DNA complexes can be trapped and analyzed

103 ne the rate of cross-link reversal for cross-linked protein-DNA complexes from yeast cell lysate.

104 ese base lesions in duplex DNA using a cross-linked protein-DNA crystallization system.

105 ases that bind and cleave the target through linked protein domains (e.g. TALENs and zinc-finger nucl

106 evation of hydrostatic pressure, the fission-linked protein, Drp-1 was translocated from the cytosol

107 es specific for glycosylphosphatidylinositol-linked proteins (e.g., CD48, CD55, and CD59).

108 Substrate Linked Protein Evolution (SLiPE) was used to optimize th

109 Robust, mechanistically-linked protein expression markers, by integrating cis- a

110 localized activation of the membrane-F-actin linking protein ezrin.

111 between EBP50 and the membrane-cytoskeletal linking protein ezrin.

112 closely related to the membrane-cytoskeleton linking proteins Ezrin, Radixin, and Moesin, and localiz

113 s (potentially containing new members of the link protein family), in which other chondroitin sulfate

114 Recent studies showed that the actin cross-linking protein, fascin, undergoes rapid cycling between

115 y actin bundles assembled by the actin cross-linking protein, fascin.

116 investigate the behaviors of two actin cross-linking proteins, fascin and alpha-actinin, during the f

117 ll GTPase Rab1A as well as the F-actin cross-linking protein filamin (actin-binding protein 120, abp1

118 Depletion of the actin cross-linking protein filamin A (FlnA) causes a collapse of th

119 esis that interactions between F-actin cross-linking protein filamin A and caveolin-1 facilitate the

120 entified the non-muscle actin filament cross-linking protein filamin A as a novel Gag binding partner

121 The actin cross-linking protein Filamin has an important role in the con

122 so interacted with the mammalian actin cross-linking protein filamin in the yeast two-hybrid assay th

123 skeleton by interacting with the actin cross-linking protein filamin.

124 The actin cross-linking protein, filamin (Fln), has been implicated in t

125 ctivation), whereas binding of another actin-linking protein, filamin, to the integrin beta CTs negat

126 ssociated protein AFAP-110 is an actin cross-linking protein first identified as a substrate of the v

127 ning stable polymers and can open avenues to link protein folding to jamming theory.

128 (374)ALGS) fragments as well as biglycan and link protein from the aortic wall.

129 ydrolyzing PI and cleaving glycosyl-PI (GPI)-linked proteins from cell surfaces.

130 ly become appreciated as a modification that links protein function to cellular oxidative status.

131 ed to the identification of 50 potential Trx-linked proteins functional in 12 processes: photorespira

132 The targeted disruption of cartilage link protein gene (Crtl1) in homozygous mice resulted in

133 Herein, enzymes in the N-linked protein glycosylation (Pgl) pathway of Campylobac

134 olyprenol reductase with a crucial role in N-linked protein glycosylation and pinpoint SRD5A3 mutatio

135 Changes in O-linked protein glycosylation are known to correlate with

136 ome underscores the importance of asparagine-linked protein glycosylation for proper functioning of t

137 Our findings underscore the importance of N-linked protein glycosylation for proper functioning of t

138 framework for understanding the process of N-linked protein glycosylation in Bacteria and for devisin

139 D-glucosamine, along with decreased O- and N-linked protein glycosylation in patients' cells.

140 N-Linked protein glycosylation is a frequent post-translat

141 N-Linked protein glycosylation is a very common post-trans

142 N-Linked protein glycosylation is an essential and highly

143 Asparagine-linked protein glycosylation is essential for the virule

144 N-Linked protein glycosylation is one of the most prevalen

145 N-linked protein glycosylation occurs in all three branche

146 The O-linked protein glycosylation pathway in Neisseria gonorr

147 Campylobacter jejuni has an N-linked protein glycosylation pathway that is required fo

148 s recently discovered to contain a general N-linked protein glycosylation pathway.

149 dependent acetyltransferase in both N- and O-linked protein glycosylation pathways.

150 yme catalyzing the first committed step of N-linked protein glycosylation.

151 the GALNT enzyme in initiating mucin type O-linked protein glycosylation.

152 by tunicamycin (TM), an agent that blocks N-linked protein glycosylation.

153 ampylobacter jejuni has systems for N- and O-linked protein glycosylation.

154 opneumoniae encodes an unusual pathway for N-linked protein glycosylation.

155 the first two committed steps of asparagine-linked protein glycosylation.

156 since the discovery of asparagine-linked (N-linked) protein glycosylation pathways in bacteria, majo

157 llapse radially due to the activity of cross-linking proteins, hence producing conical-shaped filamen

158 oxyl terminus of protocadherin 15 CD3, a tip link protein implicated in mechanosensory transduction.

159 As such, Tim54p links protein import, assembly, and turnover pathways in

160 some mothers develop antibodies against a Y-linked protein important in male brain development, and

161 Immune assays targeting two Y-linked proteins important in brain development-protocadh

162 levels coding for aggrecan, collagen II, and link protein in chondrocytes exposed to endoplasmic reti

163 xamined for the first time the expression of link proteins in human brain and malignant gliomas.

164 three-dimensional matrixes composed of cross-linked protein in cellular and microfluidic environments

165 s that females have, yet the expression of X-linked proteins in males is the same because of a sex-sp

166 proteomic approaches to identify soluble Trx-linked proteins in mitochondria isolated from photosynth

167 Our results indicate a role for GPI-linked proteins in NK cell subset homeostasis and sugges

168 he role of typical Rho GTPases and other Rho-linked proteins in synaptic plasticity and cognitive fun

169 1 along with collagen biosynthesis and cross-linking protein in HG condition.

170 The role of actin cross-linking proteins in cortical dynamics is still incomplet

171 f cellular localization of known actin cross-linking proteins in mouse melanoma B16F1 cells revealed

172 aracterized actin-filament bundling or cross-linking proteins in plants and each is encoded by a mult

173 ross-linking proteins, but the role of cross-linking proteins in the initial steps of structure forma

174 of filamin A (FLNa), an actin filament cross-linking protein, in wound contraction and maintenance of

175 Additional evolutionarily linked proteins include a thioredoxin reductase homolog

176 In this study, we examined whether tip-link proteins, including Cadherin 23 (Cdh23), regulate A

177 oposed that the partial proteolysis of cross-linked proteins into smaller oligopeptides constitutes a

178 d accumulation of polyubiquitinated (K48/K63-linked) proteins into juxtanuclear aggresomes, without a

179 ncrease the expression of one of these cross-linked proteins, involucrin, and that this effect can be

180 identified filamin A (FLNa), an actin-cross-linking protein involved in cell movement, as a bona fid

181 rotein that regulates the Arp2/3 complex and links proteins involved in endocytosis to the actin cyto

182 indicate that the conformation of the cross-linked protein is non-native.

183 e; subsequently, DNA together with all cross-linked proteins is isolated by centrifugation under dena

184 osylated, glycosylphosphatidylinositol (GPI)-linked protein, is expressed preferentially by myofiber

185 Lysyl oxidase (LOX), a matrix cross-linking protein, is known to be selectively expressed an

186 alpha-actinin and palladin, two actin-cross-linking proteins, is essential for proper bidirectional

187 (also known as Shotgun) and the microtubule-linked proteins Katanin-60, EB1, Milton and aPKC.

188 Integrin-linked protein kinase was identified as a positive regul

189 und to participate in multiprotein complexes linking protein kinase A to the activation of phosphodie

190 Here we present data linking protein kinase C alpha (PKCalpha) to the regulat

191 RACK1 serves as a scaffold, linking protein kinase C to its substrates.

192 that alpha actinin 4 (ACTN4), an actin-cross-linking protein known to coordinate cytoskeletal organiz

193 We have successfully linked protein library screening directly with the ident

194 key challenge in cell biology is to directly link protein localization to function.

195 There is abundant epidemiological evidence linking protein malnutrition to impaired vaccine efficac

196 h consisting of dynamic MTs and the MT-cross-linking protein MAP65-1.

197 or a d-amino acid polymer antigen in a cross-linked protein matrix was shown to be sufficient to prod

198 ymer bundles, which also suggests that cross-linking proteins may contribute to the regulation of the

199 tolithographic method for constructing cross-linked protein microstructures, permits one to compartme

200 ggest that CHOP is a fundamental factor that links protein misfolding in the ER to oxidative stress a

201 Glyoxal acted faster than PFA, cross-linked proteins more effectively, and improved the prese

202 Link protein N-terminal peptide (LPP) is a proteolytic f

203 Asparagine-linked protein N-glycosylation, the most complex glycosy

204 functions in the early stages of asparagine-linked protein (N-) glycosylation.

205 ases the activity and function of plasticity-linked protein networks in the amygdala that regulate th

206 it is possible that STIM1 represents a nexus linking protein O-GlcNAcylation with Ca(2+)-mediated tra

207 interactions between myosin and actin cross-linking proteins observed in cellular mechanosensation,

208 targets PI and glycosylphosphatidylinositol-linked proteins of eukaryotic cells.

209 SDS-PAGE analysis of non-covalently linked proteins of the cell wall of the mutant, compared

210 tsZ polymers, which makes it the first cross-linking protein of the bacterial cytoskeleton.

211 s lacking glycosylphosphatidylinositol (GPI)-linked proteins on their surface (GPI(neg)) exist alongs

212 It may also permit one to cross-link proteins or to obscure specific protein surfaces du

213 Actin filament cross-linking proteins organize filaments into higher order ne

214 lagen biosynthesis as well as collagen cross-linking protein, P4HA1 and PLOD2 were observed along wit

215 lly associated with actin and an actin cross-linking protein palladin.

216 t-resistant membrane domains, into which GPI-linked proteins partition, are enriched in cholesterol a

217 Mutations of the X-linked protein PHF6 cause the intellectual disability di

218 immune signaling module downstream of PRRs, linking protein phosphorylation cascades to metabolic re

219 orporation of a glycosylphosphatidylinositol-linked protein (placental alkaline phosphatase) occurred

220 volutionarily conserved actin bundling/cross-linking protein plastin is instrumental for the generati

221 Cross-linked protein-polymer surfactant films consisting of en

222 that Ubc13, an E2 enzyme that catalyzes K63-linked protein polyubiquitination, is largely dispensabl

223 Uev1a, specifically mediates lysine 63 (K63)-linked protein polyubiquitylation, a process that does n

224 identification and characterization of cross-linked proteins presents a significant analytical challe

225 repeat containing 2 (XIRP2), an actin-cross-linking protein previously reported to be specifically e

226 Our findings reveal that mTOR links protein production with quality control.

227 The tip link protein protocadherin 15 (PCDH15) is a central comp

228 ein-protein interaction between HCN1 and tip-link protein protocadherin 15 CD3, a protein-protein int

229 coupling between HCN1 and stereociliary tip-link protein protocadherin 15 has been described for a t

230 l for hearing, physically interacts with tip link protein protocadherin-15.

231 The presence of cross-linked proteins provides an analogy to mussel and barnac

232 ied by alkaline partial hydrolysis and cross-linked protein residues were identified by mass spectrom

233 denaturing washes, the resulting covalently linked protein-RNA complexes are purified with oligo(dT)

234 Systematically collected data that link protein sequence to binding are valuable for elucid

235 an intra- and intermolecular cysteine cross-linked protein shell called the chlamydial outer membran

236 However, charging the cross-linked protein solution with niosomal suspension resulte

237 to the capability to produce multiple cross-linked protein species and polymeric additions to protei

238 re activity in a ligand-dependent manner, we linked protein splicing to cell survival or fluorescence

239 r, we have utilized a genetic selection that links protein stability to antibiotic resistance to isol

240 ndroitin sulfate proteoglycan aggrecan forms link protein-stabilized complexes with hyaluronan (HA),

241 F-box proteins specify ubiquitination by linking protein substrates to the terminal E3 ligase.

242 ssumed that a specific ubiquitin ligase (E3) links protein substrates to polyubiquitin chains contain

243 Actin cytoskeleton-linked proteins such as talin, vinculin and filamin func

244 bsence of other glycosylphosphatidylinositol-linked proteins such as urokinase-type plasminogen activ

245 Gs), tenascin-R (TN-R), hyaluronan (HA), and link proteins, such as cartilage link protein 1 (Crtll).

246 duces CaMKIIalpha binding to established ASD-linked proteins, such as Shank3 and subunits of l-type c

247 onan (HA) receptor Lyve-1 is a member of the Link protein superfamily most similar to the leukocyte H

248 results suggest general physical mechanisms linking protein symmetry, the lattice architecture of me

249 propose that specialized machinery exists to link protein synthesis with class I peptide ligand gener

250 These findings link protein synthesis, insulin sensitivity, and body we

251 Binding of the actin-linking protein, talin, to integrin beta cytoplasmic tai

252 omers and physically associates with the ALS-linked proteins TDP-43 and FUS in the nucleus.

253 accurately estimates functional coupling of linked proteins than use individual data sources alone.

254 The other link protein that shows a perineuronal net pattern in th

255 Poliovirus (PV) VPg is a genome-linked protein that is essential for the initiation of v

256 y encode glycosyl-phosphatidylinositol (GPI)-linked proteins that are essential for activity of the t

257 ocol for the large-scale purification of Ubl-linked proteins that minimizes sample contamination with

258 (CaMKIIalpha) and a network of functionally linked proteins that regulate neural plasticity and glut

259 10)), encoding plectin, a cytoskeletal cross-linking protein that contributes to integrity of cardiac

260 Filamin A (FlnA) is an important actin cross-linking protein that is required for cellular processes

261 and functions as an actin stress fiber cross-linking protein that promotes the maturation of nascent

262 Spectrins are tetrameric actin-cross-linking proteins that form an elastic network, termed th

263 Filamins are actin-binding and cross-linking proteins that organize the actin cytoskeleton an

264 ave wider implications for other actin cross-linking proteins that share a villin-like headpiece doma

265 ed receptor V1 (adgrv1), another hair bundle link protein, the entry of Cdhr23- and Cdhr15-expressing

266 e 3-deoxythreosone, which modified and cross-linked proteins through the formation of an arginine add

267 anslational modification of the ECM by cross-linking proteins, thus making these proteins resistant t

268 expression of the glycophosphatidylinositol-linked protein Thy-1 affects proliferation and myofibrob

269 nriched for the glycosylphosphatidylinositol-linked protein Thy-1, the ganglioside GM1, palmitoylated

270 and glycoproteins such as the tenascins and link proteins to form the matrix scaffold.

271 mologous proteins ezrin, radixin, and moesin link proteins to the actin cytoskeleton.

272 omeostasis, or proteostasis, enables disease-linked proteins to adopt aberrant tertiary structures, a

273 to pairs of non-homologous but functionally linked proteins to find specific regions of the protein

274 ing how CLASP collaborates with functionally linked proteins to regulate MT dynamics.

275 The two thioether bonds linking protein to heme in cyt c are present in 1, and t

276 Linking proteins to PEI required no other treatment beyo

277 ross-bridge peptide of the cell wall or they link proteins together to form pili.

278 how they facilitate expanded functions that link protein translation to other cellular pathways.

279 derstanding of an important regulatory loop, linking protein turnover to gene regulation.

280 Receptor-linked protein-tyrosine phosphatases (RPTPs) are essenti

281 The central chemical step in Lys 63-linked protein ubiquitination involves the reaction of a

282 clonal antibody AGG-C1/anti-NITEGE(373)) and link proteins (using monoclonal antibody 8-A-4), as well

283 rB9-2, and VirB10 justify their testing as a linked protein vaccine against A. marginale.

284 ytosis of glycosylphosphatidylinositol (GPI)-linked proteins via a specific pathway into GPI-enriched

285 between Capsicum-eIF4E and the viral genome-linked protein (VPg) is required for the viral infection

286 s between PAP and turnip mosaic virus genome-linked protein (VPg) were investigated.

287 Potyvirus genome linked protein, VPg, interacts with translation initiati

288 alpha-Actinin-4, an actin cross-linking protein, was identified.

289 proteolysis assays on this semisynthetic ATP-linked protein, we have obtained unique evidence for an

290 n levels for aggrecan, type II collagen, and link protein were up-regulated approximately 2-3-fold du

291 air or with exogenous oxidant, and the cross-linked proteins were reconstituted to assess their funct

292 Importantly, deafness-linked proteins were significantly enriched in HCs, sugg

293 ce HA synthetic enzymes (HASs), thus HA, and link proteins, which are scaffolding molecules for an or

294 outer membrane containing a network of cross-linked proteins, which together confer cell envelope sta

295 re also developed in our laboratory by cross-linking proteins while preserving their native structure

296 se of alpha-synuclein, a Parkinson's disease-linked protein whose monomer exhibits significant disord

297 opropyl)carbodiimide (EDC) was used to cross-link proteins with complementary charged groups in close

298 pping uses gene ontology (GO) information to link proteins with similar biological functions from dif

299 e de novo computational design of multicross-linked proteins with predictable and well-defined folds,

300 microtubules are organized by numerous cross-linking proteins yet the mechanical properties of those