• 제목/요약/키워드: helical structure

검색결과 266건 처리시간 0.024초

Effects of the Hinge Region of Cecropin A(1-8)-Melittin 2(1-12), a Synthetic Antimicrobial Peptide on Antibacterial, Antitumor, and Vesicle-Disrupting Activity

  • Shin, Song-Yub;Kang, Joo-Hyun;Jang, So-Yun;Kim, KiI-Lyong;Hahm, Kyung-Soo
    • BMB Reports
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    • 제32권6호
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    • pp.561-566
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    • 1999
  • CA(1-8)-ME(1-12) [CA-ME], composed of cecropin A(1-8) and melittin(1-12), is a synthetic antimicrobial peptide having potent antibacterial and antitumor activities with minimal hemolytic activity. In order to investigate the effects of the flexible hinge sequence, Gly-Ile-Gly, of CA-ME on antibiotic activity, CA-ME and three analogues, CA-ME1, CA-ME2, and CA-ME3, were synthesized. The Gly-Ile-Gly sequence of Ca-ME was deleted in CA-ME1 and replaced with Pro and Gly-Pro-Gly in CA-ME2 and CA-ME3, respectively. CA-ME1 and CA-ME3 showed a significant decrease in antitumor activity and phospholipid vesicle-disrupting ability. However, CA-ME2 showed similar antitumor and vesicle-disrupting activities, as compared with CA-ME. These results suggest that the flexibility or ${\beta}$-turn induced by Gly-Ile-Gly or Pro in the central part of CA-ME may be important in the electrostatic interaction of the N-terminus cationic ${\alpha}$-helical region with the cell membrane surface and the hydrophobic interaction of the C-terminus amphipathic ${\alpha}$-helical region with the hydrophobic acyl chains in the cell membrane. CA-ME3 exhibited lower antitumor and vesicle-disrupting activities than CA-ME and CA-ME2. This result suggests that the excessive ${\beta}$-turn structure caused by the Gly-Pro-Gly sequence in CA-ME3 seems to interrupt ion channel/pore formation in the lipid bilayer. We concluded that the appropriate flexibility or bilayer. We concluded that the appropriate flexibility or ${\beta}$-turn structure provided by the central hinge is responsible for the effective antibiotic activity of the antimicrobial peptides with the helix-hinge-helix structure.

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Structure and Bacterial Cell Selectivity of a Fish-Derived Antimicrobial Peptide, Pleurocidin

  • Yang Ji-Young;Shin Song-Yub;Lim Shin-Saeng;Hahm Kyung-Soo;Kim Yang-Mee
    • Journal of Microbiology and Biotechnology
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    • 제16권6호
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    • pp.880-888
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    • 2006
  • Pleurocidin, an $\alpha$-helical cationic antimicrobial peptide, was isolated from skin mucosa of winter flounder (Pleuronectes americamus). It had strong antimicrobial activities against Gram-positive and Gram-negative bacteria, but had very weak hemolytic activity. The Gly$^{13,17}\rightarrow$Ala analog (pleurocidin-AA) showed similar antibacterial activities, but had dramatically increased hemolytic activity. The bacterial cell selectivity of pleurocidin was confirmed through the membrane-disrupting and membrane-binding affinities using dye leakage, tryptophan fluorescence blue shift, and tryptophan quenching experiments. However, the non-cell-selective antimicrobial peptide, pleurocidin-AA, interacts strongly with both negatively charged and zwitterionic phospholipid membranes, the latter of which are the major constituents of the outer leaflet of erythrocytes. Circular dihroism spectra showed that pleurocidin-AA has much higher contents of $\alpha$-helical conformation than pleurocidin. The tertiary structure determined by NMR spectroscopy showed that pleurocidin has a flexible. structure between the long helix from $Gly^3$ to $Gly^{17}$ and the short helix from $Gly^{17}$ to $Leu^{25}$. Cell-selective antimicrobial peptide pleurocidin interacts strongly with negatively charged phospholipid membranes, which mimic bacterial membranes. Structural flexibility between the two helices may play a key role in bacterial cell selectivity of pleurocidin.

섬유체적비 불균일 및 수지응집층이 복합재 격자 구조체 리브의 강성도 거동에 미치는 영향 (The Effect of the Fiber Volume Fraction Non-uniformity and Resin Rich Layer on the Rib Stiffness Behavior of Composite Lattice Structures)

  • 강민송;전민혁;김인걸;김문국;고은수;이상우
    • Composites Research
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    • 제31권4호
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    • pp.161-170
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    • 2018
  • 원통형 복합재 격자 구조체는 필라멘트 와인딩 기법으로 제작되며 제작 공정에서 발생할 수 있는 섬유체적비 불균일과 수지응집층은 구조체의 강성도 및 강도에 영향을 줄 수 있다. 구조체의 주요 요소인 후프 및 헬리컬 리브의 단면 분석을 통해 섬유체적비 불균일 및 수지응집층의 존재 여부를 확인하였으며, 단면 분석 결과를 바탕으로 후프 및 헬리컬 리브에 대한 실험 및 이론적 접근을 통해 섬유체적비 불균일 및 수지응집층이 리브 요소의 강성도에 미치는 영향을 분석하였다. 섬유체적비 불균일이 후프 리브의 굽힘 거동에 영향을 미치는 것을 확인하였으며 헬리컬 리브의 경우 섬유체적비 불균일 및 수지응집층에 의해 강성도에 변화가 있음을 확인하였다.

Alcohol and Temperature Induced Conformational Transitions in Ervatamin B: Sequential Unfolding of Domains

  • Kundu, Suman;Sundd, Monica;Jagannadham, Medicherla V.
    • BMB Reports
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    • 제35권2호
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    • pp.155-164
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    • 2002
  • The structural aspects of ervatamin B have been studied in different types of alcohol. This alcohol did not affect the structure or activity of ervatamin B under neutral conditions. At a low pH (3.0), different kinds of alcohol have different effects. Interestingly, at a certain concentration of non-fluorinated, aliphatic, monohydric alcohol, a conformational switch from the predominantly $\alpha$-helical to $\beta$-sheeted state is observed with a complete loss of tertiary structure and proteolytic activity. This is contrary to the observation that alcohol induces mostly the $\alpha$helical structure in proteins. The O-state of ervatamin B in 50% methanol at pH 3.0 has enhanced the stability towards GuHCl denaturation and shows a biphasic transition. This suggests the presence of two structural parts with different stabilities that unfold in steps. The thermal unfolding of ervatamin B in the O-state is also biphasic, which confirms the presence of two domains in the enzyme structure that unfold sequentially. The differential stabilization of the structural parts may also be a reflection of the differential stabilization of local conformations in methanol. Thermal unfolding of ervatamin B in the absence of alcohol is cooperative, both at neutral and low pH, and can be fitted to a two state model. However, at pH 2.0 the calorimetric profiles show two peaks, which indicates the presence of two structural domains in the enzyme with different thermal stabilities that are denatured more or less independently. With an increase in pH to 3.0 and 4.0, the shape of the DSC profiles change, and the two peaks converge to a predominant single peak. However, the ratio of van't Hoff enthalpy to calorimetric enthalpy is approximated to 2.0, indicating non-cooperativity in thermal unfolding.

Effect of Double Replacement of L-Pro, D-Pro, D-Leu or Nleu in Hydrophobic Face of Amphipathic α-Helical Model Antimicrobial Peptide on Structure, Cell Selectivity and Mechanism of Action

  • Shin, Song Yub
    • Bulletin of the Korean Chemical Society
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    • 제35권11호
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    • pp.3267-3274
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    • 2014
  • In order to investigate the effects of the double replacement of $\small{L}$-Pro, $\small{D}$-Pro, $\small{D}$-Leu or Nleu (the peptoid residue for Leu) in the hydrophobic face (positions 9 and 13) of amphipathic ${\alpha}$-helical non-cell-selective antimicrobial peptide $L_8K_9W_1$ on the structure, cell selectivity and mechanism of action, we synthesized a series of $L_8K_9W_1$ analogs with double replacement of $\small{L}$-Pro, $\small{D}$-Pro, $\small{D}$-Leu or Nleu in the hydrophobic face of $L_8K_9W_1$. In this study, we have confirmed that the double replacement of $\small{L}$-Pro, $\small{D}$-Pro, or Nleu in the hydrophobic face of $L_8K_9W_1$ let to a great increase in the selectivity toward bacterial cells and a complete destruction of ${\alpha}$-helical structure. Interestingly, $L_8K_9W_1$-$\small{L}$-Pro, $L_8K_9W_1$-$\small{D}$-Pro and $L_8K_9W_1$-Nleu preferentially interacted with negatively charged phospholipids, but unlike $L_8K_9W_1$ and $L_8K_9W_1$-$\small{D}$-Leu, they did not disrupt the integrity of lipid bilayers and depolarize the bacterial cytoplasmic membrane. These results suggested that the mode of action of $L_8K_9W_1$-$\small{L}$-Pro, $L_8K_9W_1$-$\small{D}$-Pro and $L_8K_9W_1$-Nleu involves the intracellular target other than the bacterial membrane. In particular, $L_8K_9W_1$-$\small{L}$-Pro, $L_8K_9W_1$-$\small{D}$-Pro and $L_8K_9W_1$-Nleu had powerful antimicrobial activity (MIC range, 1 to $4{\mu}M$) against methicillin-resistant Staphylococcus aureus (MRSA) and multidrug-resistant Pseudomonas aeruginosa (MDRPA). Taken together, our results suggested that $L_8K_9W_1$-$\small{L}$-Pro, $L_8K_9W_1$-$\small{D}$-Pro and $L_8K_9W_1$-Nleu with great cell selectivity may be promising candidates for novel therapeutic agents, complementing conventional antibiotic therapies to combat pathogenic microorganisms.

Effect of γ-Irradiation on the Molecular Properties of Bovine Serum Albumin and β-Lcatoglobulin

  • Cho, Yong-Sik;Song, Kyung-Bin
    • BMB Reports
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    • 제33권2호
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    • pp.133-137
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    • 2000
  • To elucidate the effect of oxygen radicals on the molecular properties of proteins, the secondary and tertiary structure and molecular weight size of BSA and ${\beta}$-lactoglobulin were examined after irradiation of proteins at various doses. Gamma-irradiation of protein solutions caused the disruption of the ordered structure of protein molecules as well as degradation, cross-linking, and aggregation of the polypeptide chains. As a model system, BSA and ${\beta}$-lactoglobulin were used as a typical ${\alpha}$-helical and a ${\beta}$-sheet structure protein, respectively. A circular dichroism study showed that the increase of radiation decreased the ordered structure of proteins with a concurrent increase of aperiodic structure content. Fluorescence spectroscopy indicated that irradiation quenched the emission intensity excited at 280 nm. SDS-PAGE and a gel permeation chromatography study indicated that radiation caused initial fragmentation of proteins resulting in a subsequent aggregation due to cross-linking of protein molecules.

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수소 결합을 통한 Helix 폴리 펩타이드사이의 복합체 형성 (Intermacromolecular Complex Formation between Helix Strilctilral Polypeptides through Hydrogen Bonding)

  • 조병기;김창규
    • 대한화장품학회지
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    • 제18권1호
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    • pp.99-132
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    • 1992
  • 물-알코올 용액에서 염기성으로 작용하는 폴리펩타이드와 산성으로 작용하는 폴리펩타이드 사이에 수소결합을 통한 복합체 형성에 관한 연구를 점도, PH, 빛산란, 원편광이색성, 광회전도 등으로 조사했다. 얻어진 결과는 여러가지 복합체 시스템 모두가 1:2 조성으로 복합체 형성을 한다는 것을 알 수 있었으며, 우선성 헬릭스를 가지는 폴리펩타이드와 좌선성 헬릭스를 가지는 폴리펩타이드, 즉 반대방향성의 헬릭스 구조를 가지는 폴리펩타이드들 사이에 강한 상호작용을 나타내고, 반면, 같은 방향성의 헬릭스 구조를 가지는 폴리펩타이드의 형태가 복합체 형성에 매우 중요한 역할을 한다는 것을 나타낸다. 즉, 입체선택적 복합체 형성을 보인다. 또한 구조적으로 유연한 구조를 가지는 폴리펩타이드가 강한 상호 작용을 나타낸다. 즉, PHPL보다 PLP(I)이, PLP(I)보다 PLP(II)가, PAA보다 PGA가 더 강한 상호작용을 나타낸다. 이런 상호 복합체 형성이 일어나면 형태전이가 일어난다는 것도 확인할 수 있었다. 위의 결과를 근거로 하여, 좌선성 헬릭스 구조의 모발의 케라틴에 PLP(I, II)와 PHLP를 흡착시킨 후, 흡착량을 HPLC로 측정한 결과, PLP(II)보다 PLP(I)이, PHLP보다 PLP(II)가 더 많이 흡착되었다. 결론적으로, 모발에 폴리펩타이드를 사용시, 좌선성헬릭스 구조의 폴리펩타이드 보다 우선성헬릭스 구조의 폴리펩타이드가 더 많이 흡착되고, rigid conformation의 폴리펩타이드보다 foexible conformation의 폴리펩타이드가 더 많이 모발에 흡착되어, 효과가 좋다는 것을 알 수 있다.

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붉은머리 오목눈이 (Paradoxornis webbiana)의 정자변태 과정 중 정자형성세포의 미세구조 (Fine Structure of the Spermatogenic Cells during the Spermiogenesis of Paradoxornis webbiana)

  • 이정훈;함규황
    • Applied Microscopy
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    • 제31권3호
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    • pp.245-256
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    • 2001
  • 본 연구는 붉은머리오목눈이(Paradoxornis webbiana)의 정자변태 과정을 알아보기 위하여 전자현미경으로 세포분화 단계에 따른 세포구조물의 특징을 기초로 하여 관찰한 결과 정자변태의 전과정을 10단계로 나타내었다. 염색질의 변화는 골지기에서 균질한 섬유상의 형태가 두모기에서는 서서히 응축하여 첨체기에 막대상으로 응축되고 성숙기에 이르러 더욱 응축되고, 균질화되어 완전한 핵을 형성하였다. 꼬리의 형성시기는 초기 골지단계에서 시작하여 성숙후기에 완료되었다. 축사는 9+2구조이며, 미토콘드리아 다발은 2개가 1조를 이루어 축사를 중심으로 $15^{\circ}$ 각도로 규칙적으로 배열되어 있었다. 그리고 microtubules들이 미토콘드리아 외막을 둘러싸고 있었다 정자의 파동막의 형태는 S자형으로 정자원형질막을 둘러싸고 있었다.

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Effects of Temperature and Additives on the Thermal Stability of Glucoamylase from Aspergillus niger

  • Liu, Yang;Meng, Zhaoli;Shi, Ruilin;Zhan, Le;Hu, Wei;Xiang, Hongyu;Xie, Qiuhong
    • Journal of Microbiology and Biotechnology
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    • 제25권1호
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    • pp.33-43
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    • 2015
  • GAM-1 and GAM-2, two themostable glucoamylases from Aspergillus niger B-30, possess different molecular masses, glycosylation, and thermal stability. In the present study, the effects of additives on the thermal inactivation of GAM-1 and GAM-2 were investigated. The half-lives of GAM-1 and GAM-2 at 70℃ were 45 and 216 min, respectively. Data obtained from fluorescence spectroscopy, circular dichroism spectroscopy, UV absorption spectroscopy, and dynamic light scattering demonstrated that during the thermal inactivation progress, combined with the loss of the helical structure and a majority of the tertiary structure, tryptophan residues were partially exposed and further led to glucoamylases aggregating. The thermal stability of GAM-1 and GAM-2 was largely improved in the presence of sorbitol and trehalose. Results from spectroscopy and Native-PAGE confirmed that sorbitol and trehalose maintained the native state of glucoamylases and prevented their thermal aggregation. The loss of hydrophobic bonding and helical structure was responsible for the decrease of glucoamylase activity. Additionally, sorbitol and trehalose significantly increased the substrate affinity and catalytic efficiency of the two glucoamylases. Our results display an insight into the thermal inactivation of glucoamylases and provide an important base for industrial applications of the thermally stable glucoamylases.

21톤급 휠 굴착기용 트랜스미션의 기어 트레인에 대한 강도 해석 (Strength Analysis of Complex Gear Train for Transmission of 21-Ton Grade Wheel Excavator)

  • 이준희;배명호;조연상
    • Tribology and Lubricants
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    • 제38권5호
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    • pp.179-184
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    • 2022
  • The power train of transmission for 21-ton grade wheel excavator makes use of a complex gear train composed of a planetary and helical gear system to drive the wheel excavator by transmitting power to the axle. The complex gear train with a shift mode is an important part of the transmission because of strength problems in an extreme environment. To calculate the specifications of the complex gear train and analyze the gear bending and compressive stresses of the complex gear train, this study analyzes gear bending and compressive stresses accurately for the optimal design of the complex gear train with respect to cost and reliability. In this article, the gear bending and compressive stresses of the complex gear train are calculated using the Lewes and Hertz equation. Evaluating the results with the data of the allowable bending and compressive stress from the stress and number of cycles curves of the gears verified the calculated specifications of the complex gear train. A computer structure analysis is performed with the 3D model of the planetary and helical gears to analyze the structure strength of the complex gear train. The results demonstrate that the durability and strength of the complex gear train are safe, because the safety factors of the bending and compressive stresses are more than 1.0.