Perfect Binding Research Articles

Primer extension refractory PCR: an efficient and reliable genome walking method.

Genome walking, a molecular technique for obtaining unknown flanking genomic sequences from a known genomic sequence, has been broadly applied to determine transgenic sites, mine new genetic resources, and fill in chromosomal gaps. This technique has advanced genomics, genetics, and related disciplines. Here, an efficient and reliable genome walking technique, called primer extension refractory PCR (PER-PCR), is presented. PER-PCR uses a set of primary, secondary, and tertiary walking primers. The middle 15 nt of the primary walking primer overlaps with the 3' parts of the secondary and tertiary primers. The 5' parts of the three primers are heterologous to each other. The short overlap allows the walking primer to anneal to its predecessor only in a relaxed-stringency PCR cycle, resulting in a series of single-stranded DNAs; however, the heterologous 5' part prevents the creation of a perfect binding site for the walking primer. In the next stringent cycle, the target single strand can be extended into a double-stranded DNA molecule by the sequence-specific primer and thus can be exponentially amplified by the remaining stringent cycles. The nontarget single strand fails to be enriched due to the lack of a perfect binding site for any primer. PER-PCR was validated by extension into unknown flanking regions of the hyg gene in rice and the gadR gene in Levilactobacillus brevis CD0817. In summary, in this study, a new practical PER-PCR method was constructed as a potential alternative to existing genome walking methods.

Potent ROS inhibitors from Zanthoxylum armatumDC of Nepali origin

A bioassay-guided isolation on the plant Zanthoxylum armatum DC yielded compounds tambulin (1), and prudomestin (2), from ethyl acetate fraction which showed the highest ROS inhibiting activity (IC50 = 17.8 ± 1.1 µg/mL). Structure elucidation of pure compounds was done using mass and NMR spectroscopic techniques. Compounds 1 and 2 revealed potent ROS inhibition with IC50 = 7.5 ± 0.3 and 1.5 ± 0.3 µg/mL, respectively, as compared to standard ibuprofen (IC50 = 11.2 ± 1.9 µg/mL). Likewise, both compounds 1 and 2 showed potent antioxidant activity with IC50 = 32.65 ± 0.31 and 26.96 ± 0.19 µg/mL, respectively. In vitro studies were supported by molecular docking and drug-likeliness properties. In silico studies of 1 and 2 with cyclooxygenase-2 (COX-2) showed perfect binding affinity with binding energies of −8.4 and −8.6 kcal/mol, respectively, comparable to standard ibuprofen (−7.7 kcal/mol). Drug likeness and ADMET showed higher gastrointestinal absorption of 1 and 2 and no toxic impact.

Efficiency of the dye from Spinacia olerace linn for augmentation of charge transfer to Tio2 in dye sensitized solar cell

A chlorophyll-rich dye was made from the leaves of Spinaciaoleracealinn using ethanol and a TiO2 nanoparticle-coated FTO substrate immersed in the dye to achieve ideal binding to maximize absorption of photon energy. The dye's visible light absorbance ranges from 400 nm to 700 nm, with a notable peak at 657 nm and the existence of functional groups allowing perfect binding to the semiconductor material. oxide was confirmed by UV–Visible and FTIR spectroscopy. The SEM image of the dye-impregnated TiO2-coated FTO shows a uniform dispersion of the dye over the entire surface for better photon absorption. Dye-sensitive solar cells are made using a graphene-based counter electrode and an electrolyte of the redox pair I-/I-3. The bonding characteristics of the fabricated solar cells were analyzed to predict the solar cell parameters, and it was found that the fabricated solar cells produced 0.78% efficiency with open circuit voltage., short circuit current, current density and fill factor are 0.49 V., 2.01 mA/cm2 and 0.54 respectively.

Semi-Site-Specific Primer PCR: A Simple but Reliable Genome-Walking Tool

Genome-walking has been frequently applied to molecular biology and related areas. Herein, a simple but reliable genome-walking technique, termed semi-site-specific primer PCR (3SP-PCR), is presented. The key to 3SP-PCR is the use of a semi-site-specific primer in secondary PCR that partially overlaps its corresponding primary site-specific primer. A 3SP-PCR set comprises two rounds of nested amplification reactions. In each round of reaction, any primer is allowed to partially anneal to the DNA template once only in the single relaxed-stringency cycle, creating a pool of single-stranded DNAs. The target single-stranded DNA can be converted into a double-stranded molecule directed by the site-specific primer, and thus can be exponentially amplified by the subsequent high-stringency cycles. The non-target one cannot be converted into a double-strand due to the lack of a perfect binding site to any primer, and thus fails to be amplified. We validated the 3SP-PCR method by using it to probe the unknown DNA regions of rice hygromycin genes and Levilactobacillus brevis CD0817 glutamic acid decarboxylase genes.

Guidelines on Designing MicroRNA Sponges: From Construction to Stable Cell Line.

Single microRNA (miRNA) can be inhibited using antagomiR which efficiently knocks down a specific miRNA. However, the effect is transient and often results in subtle phenotype. Here we report a guideline on designing miRNA sponges inhibiting a miRNA family. As a model system, we targeted miR-30 family, known as tumor suppressor miRNAs in multiple tumors. To achieve an efficient knockdown, we generated perfect and bulged-matched miRNA binding sites (MBS) and introduced multiple copies of MBS. The protocol here demonstrates the miRNA sponge as a useful tool to examine the functional impact of inhibition miRNAs.

Recognition of a Flexible Protein Loop in Taspase 1 by Multivalent Supramolecular Tweezers.

Many natural proteins contain flexible loops utilizing well-defined complementary surface regions of their interacting partners and usually undergo major structural rearrangements to allow perfect binding. The molecular recognition of such flexible structures is still highly challenging due to the inherent conformational dynamics. Notably, protein-protein interactions are on the other hand characterized by a multivalent display of complementary binding partners to enhance molecular affinity and specificity. Imitating this natural concept, we here report the rational design of advanced multivalent supramolecular tweezers that allow addressing two lysine and arginine clusters on a flexible protein surface loop. The protease Taspase 1, which is involved in cancer development, carries a basic bipartite nuclear localization signal (NLS) and thus interacts with Importin α, a prerequisite for proteolytic activation. Newly established synthesis routes enabled us to covalently fuse several tweezer molecules into multivalent NLS ligands. The resulting bi- up to pentavalent constructs were then systematically compared in comprehensive biochemical assays. In this series, the stepwise increase in valency was robustly reflected by the ligands' gradually enhanced potency to disrupt the interaction of Taspase 1 with Importin α, correlated with both higher binding affinity and inhibition of proteolytic activity.

A Simple Two-Dimensional Convective-Diffusive Based Modelling Study of a Biosensor for Glucose Detection

Over the past decade, novel technologies for biomolecular detection of target molecules of interest have been reported. The chemical reactions that govern the kinetics of the transport of target molecules to the sensor are also of significant importance. Here we analyze how the diffusion, convection, and reaction kinetics can drive the experimental design of a simple glucose biosensor. In this work, a physically intuitive and practical understanding of analyte transport is presented by modelling and simulating a two-dimensional convective-diffusive transport phenomenon in COMSOL Multiphysics to understand the mechanism of surface capture dynamics of a biosensor under the assumption of perfect binding kinetics. The target molecule of interest is glucose. In the model, 1 mol/m3 of the glucose solution is introduced at the inlet at 1 mm/s, and the process is simulated as a stationary study. It was found that by decreasing the flow rate, a threshold exists where the detection of target molecules by the sensor is solely controlled by diffusion. Comparison of convective and diffusive fluxes of the system as well as the concentration distribution reveal that a decrease in flow rate increases diffusive transport, thus increasing the fraction of target molecules that are captured by the sensor.

The Assessment of Anticancer and VEGFR-2 Inhibitory Activities of a New 1H-Indole Derivative: In Silico and In Vitro Approaches

Corresponding to the reported features of anti-VEGFR-2-approved compounds, a new 1H-indole derivative (compound 7) was designed. The inhibitory potential of the designed compound was revealed via a molecular docking study that showed the appropriate binding. Then, MD simulation (six studies) over a period of 100 ns was performed to confirm the precise binding and optimum energy. Additionally, MM-GBSA reaffirmed the perfect binding, exhibiting a total precise energy of −40.38 Kcal/Mol. The MM-GBSA experiments named the essential amino acids in the protein–ligand interaction, employing the binding energy decomposition and revealing the diversity of interactions of compound 7 inside the VEGFR-2 enzyme. As compound 7 is new, DFT experiments were utilized for molecular structure optimization. Additionally, the DFT results validated the coherent interaction of compound 7 with the VEGFR-2 enzyme. A good value of drug-likeness of compound 7 was acknowledged via in silico ADMET studies. Interestingly, the experimental in vitro prohibitory potential of compound 7 was better than that of sorafenib, demonstrating an IC50 value of 25 nM. Notably, the strong inhibitory effects of compound 10 against two cancer cell lines (MCF-7 and HCT 116) were established with IC50 values of 12.93 and 11.52 μM, disclosing high selectivity indexes of 6.7 and 7.5, respectively.

Ca-Al LDH hybrid self-healing microcapsules for corrosion protection

Ca-Al LDH hybrid self-healing microcapsules were fabricated with tung oil as core and ethyl cellulose (EC) as wall via solvent evaporation method. The self-healing and chlorine adsorption properties of hybrid microcapsules in cement-based materials were investigated. The corrosion resistance performance of microcapsules in simulated chlorine-contaminated concrete pore solution (SCPS) was characterized by electrochemical probe technique. First-principles based on density functional theory was applied to study the hybrid mechanism of Ca-Al LDH on self-healing microcapsules. The results demonstrate that the nano-layered Ca-Al LDH within the hybrid wall provided additional nucleation sites for cement hydration. The chlorine adsorption capacity of cement paste doped with 3 wt% and 6 wt% microcapsules was 14.7% and 26.7% higher than that of pure cement paste in SCPS, respectively. Hybrid microcapsules improved the anticorrosion of steel bars in SCPS by coupling effect of self-healing and chlorine resistance. The formation of Ca-Al LDH@EC hybrid materials is an exothermic process with perfect binding stability. The chlorine adsorption property of microcapsules was improved by the interface charge redistribution of Ca-Al LDH@EC hybrid materials.

Wristwatch PCR: A Versatile and Efficient Genome Walking Strategy.

Genome walking is a method used to retrieve unknown flanking DNA. Here, we reported wristwatch (WW) PCR, an efficient genome walking technique mediated by WW primers (WWPs). WWPs feature 5′- and 3′-overlap and a heterologous interval. Therefore, a wristwatch-like structure can be formed between WWPs under relatively low temperatures. Each WW-PCR set is composed of three nested (primary, secondary, and tertiary) PCRs individually performed by three WWPs. The WWP is arbitrarily annealed somewhere on the genome in the one low-stringency cycle of the primary PCR, or directionally to the previous WWP site in one reduced-stringency cycle of the secondary/tertiary PCR, producing a pool of single-stranded DNAs (ssDNAs). A target ssDNA incorporates a gene-specific primer (GSP) complementary at the 3′-end and the WWP at the 5′-end and thus can be exponentially amplified in the next high-stringency cycles. Nevertheless, a non-target ssDNA cannot be amplified as it lacks a perfect binding site for any primers. The practicability of the WW-PCR was validated by successfully accessing unknown regions flanking Lactobacillus brevis CD0817 glutamate decarboxylase gene and the hygromycin gene of rice. The WW-PCR is an attractive alternative to the existing genome walking techniques.

Synthesis, Characterization and Screening of Some Novel 2-Methyl-N'- [(Z)-Substituted-Phenyl ethylidene] Imidazo [1, 2-a] Pyridine-3-Carbohy drazide Derivatives as DPP-IV Inhibitors for the Treatment of Type 2 Diabetes Mellitus

Background: One of the leading global metabolic diseases marked by insulin resistance and chronic hyperglycemia is type 2 diabetes mellitus (T2DM). Since the last decade, DPP-4 enzyme inhibition has proven to be a successful, safe, and well-established therapy for the treatment of T2DM. Objective: The present work reports the synthesis, characterization, and screening of some novel 2- methyl-N'-[(Z)-substituted-phenyl ethylidene] imidazo [1, 2-a] pyridine-3-carbohydrazide derivatives as DPP-IV inhibitors for the treatment of T2DM. Methods: The molecular docking was performed to study these derivatives' binding mode in the enzyme's allosteric site. All the synthesized compounds were subjected for DPP-IV enzyme assay and in vivo antihyperglycemic activity in STZ-induced diabetic rats. Results: The synthesized derivatives exhibited potent antidiabetic activity as compared to the standard drug Sitagliptin. Out of sixteen compounds, A1, A4, B4, C2, C3, and D4 have shown promising antidiabetic activity against the DPP-IV enzyme. The most promising compound, C2, showed a percentage inhibition of 72.02±0.27 at 50 μM concentration. On the 21st-day, compound C2 showed a significant reduction in serum blood glucose level, i.e., 156.16±4.87 mg/dL, then diabetic control, which was 280.00±13.29 mg/dL whereas, standard Sitagliptin showed 133.50±11.80 mg/dL. In the in vivo antihyperglycemic activity, the compounds have exhibited good hypoglycemic potential in fasting blood glucose in the T2DM animal model. All the docked molecules have exhibited perfect binding affinity towards the active pocket of the enzyme. The synthesized derivatives were screened through Lipinski's rule of five for better optimization, and fortunately, none of them violated the rule. Conclusion: The above results indicate that compound C2 is a relatively active and selective hit molecule that can be structurally modified to enhance the DPP-IV inhibitor's potency and overall pharmacological profile. From the present work, it has been concluded that substituted pyridine-3-carbohydrazide derivatives possess excellent DPP-IV inhibitory potential and can be better optimized further by generating more in vivo, in vitro models.

CircHIPK3 Exacerbates Folic Acid-Induced Renal Tubulointerstitial Fibrosis by Sponging miR-30a.

Renal tubulointerstitial fibrosis is a common pathological feature of progressive chronic kidney disease (CKD), and current treatment has limited efficacy. The circular RNA circHIPK3 is reported to participate in the pathogenesis of various human diseases. However, the role of circHIPK3 in renal fibrosis has not been examined. In this study, we aimed to determine whether and how circHIPK3 might participate in the pathogenesis of renal fibrosis. Mice received a peritoneal injection of folic acid (250 mg/kg). Of note, 30 days later, renal fibrosis was present on periodic acid–Schiff (PAS) and Masson staining, and mRNA and protein of profibrotic genes encoding fibronectin (FN) and collagen 1 (COL1) were increased. Renal circHIPK3 was upregulated, while miR-30a was downregulated, assessed by quantitative PCR (qPCR) and fluorescence in situ hybridization (FISH). The expression of transforming growth factor beta-1 (TGF-β1) was increased by qPCR analysis, immunoblotting, and immunofluorescence. Renal circHIPK3 negatively correlated with miR-30a, and kidney miR-30a negatively correlated with TGF-β1. Target Scan and miRanda algorithms predicted three perfect binding sites between circHIPK3 and miR-30a. We found that circHIPK3, miR-30a, and TGF-β1 colocalized in the cytoplasm of human tubular epithelial cells (HK-2 cells) on FISH and immunofluorescence staining. We transfected circHIPK3 and a scrambled RNA into HK-2 cells; miR-30a was downregulated, and the profibrotic genes such as TGF-β1, FN, and COL1 were upregulated and assessed by qPCR, immunoblotting, and immunofluorescence staining. Third, the upregulation of circHIPK3, downregulation of miR-30a, and overproduction of profibrotic FN and COL1 were also observed in HK-2 cells exposed to TGF-β1. Finally, renal biopsies from patients with chronic tubulointerstitial nephritis manifested similar expression patterns of circHIPK3, miR-30a, and profibrotic proteins, such as TGF-β1, FN, and COL1 as observed in the experimental model. A feed-forward cycle was observed among circHIPK3, miR-30a, and TGF-β1. Our results suggest that circHIPK3 may contribute to progressive renal fibrosis by sponging miR-30a. circHIPK3 may be a novel therapeutic target for slowing CKD progression.

A microRNA‑17‑5p/homeobox B13 axis participates in the phenotypic modulation of vascular smooth muscle cells.

Vascular smooth muscle cells (VSMCs) serve a decisive role in intimal hyperplasia, a common pathophysiological process that leads to numerous vascular disorders. The present study aimed to investigate the unknown mechanisms underlying VSMC phenotypic modulation and identified a novel microRNA (miRNA/miR)-17-5p/homeobox B13 (HOXB13) axis involved in the phenotypic switching, proliferation and migration of VSMCs. VSMCs were isolated from the thoracic aorta of Sprague-Dawley rats, cell proliferation was determined by Cell Counting Kit-8 (CCK-8) assay, cell migration was examined by Transwell migration assay and gene expression was detected using reverse transcription-quantitative PCR and western blot analyses. It was firstly found that incubation with platelet-derived growth factor-BB (PDGF-BB) recombinant protein resulted in a significant increase in HOXB13 expression in VSMCs. Using multiple miRNA prediction tools, miR-17-5p was identified as a potential regulator for HOXB13, since it had a 7-base perfect binding site and a 5-base imperfect binding site with the 3′-untranslated region of HOXB13 mRNA, and these sequences were highly conserved across species. The regulatory effect of miR-17-5p on HOXB13 was validated using luciferase reporter assays. The expression level of miR-17-5p was increased in VSMCs under PDGF-BB stimulation, and was negatively correlated with HOXB13 mRNA and protein expression. Moreover, the miR-17-5p mimics significantly inhibited the proliferation and migration of VSMCs, while antagomiR-17-5p showed the opposite effects, which could be abolished by HOXB13 knockdown. The miR-17-5p/HOXB13 axis also regulated the expression levels of the markers of differentiated VSMCs (α-smooth muscle actin, transgelin and smoothelin), proliferating cell nuclear antigen and cell migration proteins, including MMP-2 and −9. In conclusion, the present study demonstrated that miR-17-5p inhibited the phenotypic modulation VSMCs stimulated by PDGF-BB by downregulating HOXB13, indicating that these factors may be potential therapeutic targets for intimal hyperplasia.

REVIEW OF THE STRENGTH OF FOX GLUE IN DEVELOPMENT BOOK VOLS TECHNOLOGY USING THE YOSHINO 602 ENGINE

Competition in the manufacture of raw materials for printing and binding purposes is undeniable, as is the hot glue required for binding on books. The method used in this writing is descriptive method, namely by presenting factual information obtained from observations obtained and seen in the Industrial Practices place. The binding technique without thread or perfect binding is used for binding books, magazines and others. The main ingredient in the perfect binding binding process is glue. Glue greatly affects the production result, if the adjustments are not done properly the temperature of the glue and the thickness of the glue. The purpose of writing this paper is to determine the adhesion strength of Fox brand glue and to find out the problems that occur in the gluing unit during the volume of the book "Technology Development in the Yoshino 602 machine. Fox glue has high adhesion strength and the adhesion dries quickly so as not to waste a lot of time. , Fox glue is also very suitable for binding paper types (coated and uncoated) with a temperature of 1650C-1800C and a side glue temperature of 1400C on the Yoshino 602 machine. So Fox brand glue is very suitable for the binding process of "Technology Development" books using a machine. Yoshino 602 at PT. Putra Nugraha Sentosa. The problems that occur in the gluing unit are the temperature of the glue, the thickness of the glue on the roller and the glue roller, due to the lack of accuracy of the machine operator.Keywords: Adhesion, Glue and Machine

Pillar[5]arene-Derived endo-Functionalized Molecular Tube for Mimicking Protein-Ligand Interactions.

Artificial tubular molecular pockets bearing polar functionalities on their inner surface are useful model systems for understanding the mechanisms of protein-ligand interactions in living systems. We herein report a pillar[5]arene-derived molecular tube, [P4-(OH)BPO], whose endo conformational isomer endo-[P4-(OH)BPO] possesses an inwardly pointing hydrogen-bond (H-bond) donor (OH) in its deep cavity and a strong H-bond acceptor (C═O) on its predominantly hydrophobic inner surface, rendering it a perfect protein binding pocket mimetic. A fragment-based drug design model was established using endo-[P4-(OH)BPO] and a library of various shape-complementary fragment ligands (1-38). On the basis of the binding affinity data for "fragment-pocket" complexes G⊂endo-[P4-(OH)BPO] (G = 1-38), two rationally designed "lead molecules" (39 and 40) were identified as being able to enhance binding affinity significantly by forming H-bonds with both the donor and acceptor of endo-[P4-(OH)BPO]. The described work opens new avenues for developing pillar[n]arene-derived protein binding pocket-mimetic systems for studies of protein-ligand interactions and mechanisms of enzymatic reactions.

Oxidized curdlan activates dendritic cells and enhances antitumor immunity

Curdlan activates dendritic cells (DCs) and enhances DC-based antitumor immunity. However, hydrophobicity and heterogeneity of curdlan particulates hinder perfect binding of curdlan to dectin-1 receptor, resulting in the reduced activation of antigen presenting cells and limited antitumor effects. Herein, we synthesized partially oxidized curdlan derivative (β-1,3-polyglucuronic acid, denote PGA). PGA-45 polymer, the reaction product prepared from curdlan by oxidation with 4-acetamido-TEMPO/NaClO/NaClO2 systems under acid conditions for 45 min, activated DCs, induced the expression of co-stimulatory molecules and cytokines, and promoted allogenic T cell proliferation as well as the expression of IL-2. Mechanistically, PGA-45 polymer strongly enhanced phosphorylation of IKK-β and reduced the expression of phosphorylated Akt, suggesting that PGA-45 may activate multiple cell surface receptors such as TLR4 and dectin-1. Administration of tumor lysate pulsed DCs pre-treated with PGA-45 particles induced strong antitumor activity in B16F10 melanoma model. Our data suggest that PGA-45 have strong adjuvant effects for anti-cancer immunity and the design of PGA polymers may provide insights in the development of novel adjuvants for cancer immunotherapy.

Cross of Snow: A Life of Henry Wadsworth Longfellow. By Nicholas A. Basbanes

Cross of Snow: A Life of Henry Wadsworth Longfellow. By Nicholas A. Basbanes

Identification of Potential Flavonoid Inhibitors of the SARS-CoV-2 Main Protease 6YNQ: A Molecular Docking Study

ObjectiveSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent for coronavirus disease 2019 (COVID-19), is responsible for the recent global pandemic. As there are no effective drugs or vaccines available for SARS-CoV-2, we investigated the potential of flavonoids against SARS-CoV-2 main protease 6YNQ. MethodsIn silico molecular simulation study against SARS-CoV-2 main protease 6YNQ. ResultsAmong the 21 selected flavonoids, rutin demonstrated the highest binding energy (− 8.7 kcal/mol) and displayed perfect binding with the catalytic sites. ConclusionsOur study demonstrates the inhibitory potential of flavonoids against SARS-CoV-2 main protease 6YNQ. These computational simulation studies support the hypothesis that flavonoids might be helpful for the treatment of COVID-19.

Molecular docking and simulation investigation: effect of beta-sesquiphellandrene with ionic integration on SARS-CoV2 and SFTS viruses

BackgroundAt present, viral diseases become major concern for the world. SARS-CoV2 and SFTS viruses are deadly in nature, and there is a need for developing best treatments for them. Modern in silico approaches were found to be very handy in determining putative drug molecules. In this study, we analyze interaction of beta-sesquiphellandrene (compound belongs to ginger) with spike protein (Sp) and membrane glycoprotein polyprotein (MPp). ResultsOur molecular docking and simulation study reveals the perfect binding pocket of Sp and MPp holding beta-sesquiphellandrene (bS). Binding energies for MPp-bS and Sp-bS were found to be − 9.5 kcal/mol and − 10.3 kcal/mol respectively. RMSD and RMSF values for docked complexes were found to be in selectable range, i.e., 1 to 3 Å and 1 to 8 Å respectively. Modern computational tools were used here to make this investigation fast and effective. Further, ADME analysis reveals the therapeutic validations for beta-sesquiphellandrene to act as a useful pharmacoactive compound. Beta-sesquiphellandrene provides not only inhibitory effect on spike protein of SARS-CoV2 but also similar inhibitory effects on membrane glycoprotein polyprotein complex of SFTS virus, which hampers the pathological initiation of the diseases caused by both the viruses, i.e., COVID-19 and severe fever with thrombocytopenia syndrome. ConclusionThis method of computational analysis was found to be rapid and effective, and opens new doors in the domain of in silico drug discovery. Beta-sesquiphellandrene can be used as effective medicine to control these harmful pathogens after wet lab validations.

Research of the backing technology of the book block spine

The factors influencing the backing process of the book block spine are deter-mined and their priorities are established. The method of backing the spine of book blocks in the production of publications by the method of perfect binding is proposed. This method involves gluing the backingcaptal braid to the spine of the block with a preapplied adhesive layer. The positive influence of the presence of the adhesive layer of a certain thickness on the physical and mechanical characteristics of the backing material is determined. It is established that the thickness of the blocks, the type of paper, from which the publications are made, and the direction of the cutting of the backing mate-rial is influenced by the process of backing the spine. With the growth of the tension deformation of backing materials from 1.2% (for kraft paper) to 3.8% (for the backing braid), the stability of the spine zone of the block increases to damage in the process of multiple flippers. The investigated materials in the longitudinal direction are more durable than in the transverse in 2-2.5 times, so the backed blocks can withstand 4,800 to 15,000 flippers when using kraft paper and backing braid, respectively. With the help of optical microscopy, changes in the structure of the backingcaptal braid after the multiple flippers of the book block have been investigated. It is shown that the strength of the binding of a book block depends on the choice of the method of backing. In the process of optimizing the parameters of backing the block root, various variants of linear models were tested, which are described by the functions of the dependences of the breaking forces in the longitudinal or transverse directions Z on the thickness of the block Tb. The allowable elongation of the edging material for its longitudinal and transverse cuttingV is also taken into account. The obtained models allow for the particular type of paper to pick up the necessary backing materials, which will provide a sufficient strength to the perfect binding book blocks.