ライフサイエンスコーパス: link protein

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

2 ntracellular scaffolding partner of this tip-link protein.

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

4 odon level for five of these six hair bundle link proteins.

5 re found in unique groups of six hair bundle link proteins.

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

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

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

9 multi-pass, or glycosylphosphatidylinositol-linked proteins.

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

11 conjugation to visualize and identify cross-linked proteins.

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

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

14 n and localization of identified and network-linked proteins.

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

16 g ortholog partners in pairs of functionally linked proteins.

17 luble structure composed of covalently cross-linked proteins.

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

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

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

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

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

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

24 V) and vascular stiffness, in part via 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 n moieties are substituted for the thioester-linked protein acyl-modifications through a sequence of

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

55 will support the development of novel cross-linked proteins and enable a more rational design proces

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

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

58 selective identification of dityrosine cross-linked proteins and peptides in complex biological sampl

59 The association between disease-linked proteins and stress granules further implicates i

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 Biopolymer filaments, cross-linking proteins, and enzymatically active motor protein

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

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

71 h, the actin cortex, comprising actin, cross-linking proteins, and nonmuscle myosin II (MII), begins

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

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

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

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

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

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

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

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

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

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

82 Cross-linked proteins bonded metal and wood with high strength

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

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

85 Cross-linking, protein capture and two-hybrid studies demonstr

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

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

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

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

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

91 whole exome sequence we identified two new X-linked protein coding variants that arose de novo in BAL

92 No BALB/cJ-specific X-linked protein coding variants were found, implicating i

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

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

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

96 Integral to these processes is the tip-link protein complex, which conveys force to open the in

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

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

99 This work establishes an approach for linking protein components into robust, higher-order str

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

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

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

103 hology, targeting vimentin or vimentin cross-linking proteins could provide a therapeutic approach to

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

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

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

107 pose that incorporation of BMAA into the ALS-linked protein Cu,Zn superoxide dismutase (SOD1) upon tr

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

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

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

111 New findings have linked protein, DNA, and lipid oxidation at the biochemi

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

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

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

115 Several RdRP-linked protein domains not previously detected in any RN

116 codes the glycosylphosphatidylinositol (GPI)-linked protein doppel, which is expressed on the surface

117 tes the phosphorylation of the lissencephaly-linked protein doublecortin (DCX) by cdk5/p35, but the p

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

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

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

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

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

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

124 be achieved through evaluating functionally linked protein families.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

145 Burkholderia cenocepacia O-linked protein glycosylation has been reported, but the

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

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

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

149 N-Linked protein glycosylation is an essential and highly

150 Asparagine-linked protein glycosylation is essential for the virule

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

152 N-linked protein glycosylation occurs in all three branche

153 The O-linked protein glycosylation pathway in Neisseria gonorr

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

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

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

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

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

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

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

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

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

163 ong the screen hits were genes involved in N-linked protein glycosylation.

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

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

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

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

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

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

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

171 cently labeled Bacteroides and fluorescently linked proteins in actively growing nanaerobic gut symbi

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

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

174 1 along with collagen biosynthesis and cross-linking protein in HG condition.

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

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

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

178 ation factor XIIIa (FXIIIa) covalently cross-links proteins in blood and vasculature, such as in bloo

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

180 Additional evolutionarily linked proteins include a thioredoxin reductase homolog

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

182 It is also unclear whether disease-linked proteins influence the proteome under conditions

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

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

185 In addition, microtubule and actin cross-linking protein IQGAP1 localized to fused secretory vesi

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

223 filament overlap length marked by the cross-linking protein PRC1 decreases during anaphase as chromo

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 and LigI forming a terminal structure of two linked protein rings encircling the ligated DNA.

234 denylated RNA, and apply it to recover cross-linked protein-RNA and free protein, or protein-bound RN

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

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

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

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

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

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

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

242 is perturbed upon the expression of disease-linked proteins such as FUS.

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 osed of filaments bundled by different cross-linking proteins, such as filopodia (fascin), lamellipod

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

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

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

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

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

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

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

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

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

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 ) is a complex and dynamic meshwork of cross-linked proteins that supports cell polarization and func

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

277 The receptor-linked protein tyrosine phosphatases (RPTPs) are key reg

278 The receptor-linked protein tyrosine phosphatases (RPTPs) receive cue

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

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

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

282 All nine obtained cross-linked protein versions show considerably increased ther

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

284 The potyvirus-derived viral genome-linked protein (VPg) is covalently bound to the 5' end o

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

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

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

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

294 ditions in the absence of any specific cross-linking proteins, which suggests that it is driven by ge

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