Self-assembling systems comprising intrinsically disordered protein polymers like elastin-like recombinamers

被引:12
|
作者
Juanes-Gusano, Diana [1 ]
Santos, Mercedes [1 ]
Reboto, Virginia [1 ]
Alonso, Matilde [1 ]
Rodriguez-Cabello, Jose Carlos [1 ]
机构
[1] Univ Valladolid, BIOFORGE Grp Adv Mat & Nanobiotechnol CIBER BBN, Edificio Lucia,Paseo Belen 19, Valladolid 47011, Spain
关键词
biomineralization; elastin-like recombinamers (ELRs); intrinsically disordered proteins (IDPs); order-disorder; protein domains; self-assembly; BLOCK CO-RECOMBINAMERS; NATIVELY UNFOLDED PROTEINS; FREE-ENERGY TRANSDUCTION; BIOMIMETIC MINERALIZATION; ANTIMICROBIAL PEPTIDES; UNSTRUCTURED REGIONS; DRUG-DELIVERY; CELL-ADHESION; BONE; POLYPEPTIDES;
D O I
10.1002/psc.3362
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Despite lacking cooperatively folded structures under native conditions, numerous intrinsically disordered proteins (IDPs) nevertheless have great functional importance. These IDPs are hybrids containing both ordered and intrinsically disordered protein regions (IDPRs), the structure of which is highly flexible in this unfolded state. The conformational flexibility of these disordered systems favors transitions between disordered and ordered states triggered by intrinsic and extrinsic factors, folding into different dynamic molecular assemblies to enable proper protein functions. Indeed, prokaryotic enzymes present less disorder than eukaryotic enzymes, thus showing that this disorder is related to functional and structural complexity. Protein-based polymers that mimic these IDPs include the so-called elastin-like polypeptides (ELPs), which are inspired by the composition of natural elastin. Elastin-like recombinamers (ELRs) are ELPs produced using recombinant techniques and which can therefore be tailored for a specific application. One of the most widely used and studied characteristic structures in this field is the pentapeptide (VPGXG)(n). The structural disorder in ELRs probably arises due to the high content of proline and glycine in the ELR backbone, because both these amino acids help to keep the polypeptide structure of elastomers disordered and hydrated. Moreover, the recombinant nature of these systems means that different sequences can be designed, including bioactive domains, to obtain specific structures for each application. Some of these structures, along with their applications as IDPs that self-assemble into functional vesicles or micelles from diblock copolymer ELRs, will be studied in the following sections. The incorporation of additional order- and disorder-promoting peptide/protein domains, such as alpha-helical coils or beta-strands, in the ELR sequence, and their influence on self-assembly, will also be reviewed. In addition, chemically cross-linked systems with controllable order-disorder balance, and their role in biomineralization, will be discussed. Finally, we will review different multivalent IDPs-based coatings and films for different biomedical applications, such as spatially controlled cell adhesion, osseointegration, or biomaterial-associated infection (BAI).
引用
收藏
页数:27
相关论文
共 50 条
  • [31] Cholesterol Conjugated Elastin-like Recombinamers: Molecular Dynamics Simulations, Conformational Changes, and Bioactivity
    Costa, Rui R.
    Dominguez-Arca, Vicente
    Velasco, Brenda
    Reis, Rui L.
    Rodriguez-Cabello, Jose Carlos
    Pashkuleva, Iva
    Taboada, Pablo
    Prieto, Gerardo
    ACS APPLIED MATERIALS & INTERFACES, 2024, 16 (48) : 66327 - 66340
  • [32] Bone Regeneration Mediated by a Bioactive and Biodegradable Extracellular Matrix-Like Hydrogel Based on Elastin-Like Recombinamers
    Coletta, Dante J.
    Ibanez-Fonseca, Arturo
    Missana, Liliana R.
    Jammal, Maria V.
    Vitelli, Ezequiel J.
    Aimone, Mariangeles
    Zabalza, Facundo
    Mardegan Issa, Joao P.
    Alonso, Matilde
    Carlos Rodriguez-Cabello, Jose
    Feldman, Sara
    TISSUE ENGINEERING PART A, 2017, 23 (23-24) : 1361 - 1371
  • [33] Layer-by-layer biofabrication of coronary covered stents with clickable elastin-like recombinamers
    Fernandez-Colino, Alicia
    Wolf, Frederic
    Moreira, Ricardo
    Ruetten, Stephan
    Schmitz-Rode, Thomas
    Carlos Rodriguez-Cabello, J.
    Jockenhoevel, Stefan
    Mela, Petra
    EUROPEAN POLYMER JOURNAL, 2019, 121
  • [34] The effect of NaCl on the self-assembly of elastin-like block co-recombinamers: Tuning the size of micelles and vesicles
    Pinedo-Martin, Guillermo
    Santos, Mercedes
    Testera, Ana M.
    Alonso, Matilde
    Carlos Rodriguez-Cabello, J.
    POLYMER, 2014, 55 (21) : 5314 - 5321
  • [35] Purification of an elastin-like fusion protein by microfiltration
    Ge, Xin
    Trabbic-Carlson, Kimberly
    Chilkoti, Ashutosh
    Filipe, Carlos D. M.
    BIOTECHNOLOGY AND BIOENGINEERING, 2006, 95 (03) : 424 - 432
  • [36] Modeling the Early Stages of Aggregation in Disordered Elastin-Like Proteins
    Zhang, Yue
    Zai-Rose, Valeria
    Price, Cody J.
    Bidwell, Gene L., III
    Correia, John J.
    Fitzkee, Nicholas C.
    BIOPHYSICAL JOURNAL, 2017, 112 (03) : 481A - 481A
  • [37] Biofunctionalization of REDV elastin-like recombinamers improves endothelialization on CoCr alloy surfaces for cardiovascular applications
    Isabel Castellanos, Maria
    Zenses, Anne-Sophie
    Grau, Anna
    Carlos Rodriguez-Cabello, Jose
    Javier Gil, Francisco
    Maria Manero, Jose
    Pegueroles, Marta
    COLLOIDS AND SURFACES B-BIOINTERFACES, 2015, 127 : 22 - 32
  • [38] Synthesis and characterization of new recombinant Elastin-Like Recombinamers fused to scFv for the formation of targeted polyplex
    Serrano-Ducar, S.
    Girotti, A.
    Rodriguez-Cabello, J. C.
    Arias, F. J.
    NEW BIOTECHNOLOGY, 2018, 44 : S25 - S25
  • [39] Small Caliber Compliant Vascular Grafts Based on Elastin-Like Recombinamers for in situ Tissue Engineering
    Fernandez-Colino, Alicia
    Wolf, Frederic
    Ruetten, Stephan
    Schmitz-Rode, Thomas
    Carlos Rodriguez-Cabello, Jose
    Jockenhoevel, Stefan
    Mela, Petra
    FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY, 2019, 7
  • [40] Flexible customization of the self-assembling abilities of short elastin-like peptide Fn analogs by substituting N-terminal amino acids
    Suyama, Keitaro
    Shimizu, Marin
    Maeda, Iori
    Nose, Takeru
    BIOPOLYMERS, 2022, 113 (10)