• 제목/요약/키워드: proline-rich

검색결과 89건 처리시간 0.024초

Molecular cloning and characterization of an antigenic protein with a repeating region from clonorchis sinensis

  • Kim, Tae-Yun;Kang, Shin-Yong;Ahn, Il-Young;Cho, Seung-Yull;Hong, Sung-Jong
    • Parasites, Hosts and Diseases
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    • 제39권1호
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    • pp.57-66
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    • 2001
  • In the course of immunoscreening of Clonorchis sinensis cDNA library, a cDNA CsRP12 containing a tandem repeat was isolated. The cDNA CsRP 12 encodes two putative peptides of open reading frames (ORFs) 1 and 2 (CsRP12-1 and -2). The repetitive region is composed of 15 repeats of 10 amino acids. Of the two putative peptides, CsRP12-1 was proline-rich and found to have homologues in several organisms. Recombinant proteins of the putative peptides were bacterially produced and purified by an affinity chromatography Recombinant CsRP12-1 protein was recognized by sera of clonorchiasis patients and experimental rabbits, but recombinant CsRP 12-2 was not. One of the putative peptide, CsRP12-1, is designated CsPRA, proline-rich antigen of C. sinensis. Both the C-termini of CsRP12-1 and -2 were bacterially produced and analysed to show no antigenicity. Recombinant CsPRA protein showed high sensitivity and specificity. In experimental rabbits, IgG antibodies to CsPRA was produced between 4 and 8 weeks after the infection and decreased thereafter over one you. These results indicate that CsPRA is equivalent to a natural protein and a useful antigenic protein for serodiagnosis of human clonorchiasis.

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AtbZIP16 and AtbZIP68, two new members of GBFs, can interact with other G group bZIPs in Arabidopsis thaliana

  • Shen, Huaishun;Cao, Kaiming;Wang, Xiping
    • BMB Reports
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    • 제41권2호
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    • pp.132-138
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    • 2008
  • AtbZIP16 and AtbZIP68 are two putative G group bZIP transcription factors in Arabidopsis thaliana, the other three members of G group bZIPs are GBF1-3 which can bind G-box. Members of G group have conservative protein structure: highly homological basic region and a proline-rich domain in the N-terminal region. Here, we report that AtbZIP16 and AtbZIP68 could bind cis elements with ACGT core, such as G-box, Hex, C-box and As-1, but with different binding affinities which from high to low were G-box > Hex > C-box > As-1; AtbZIP16 and AtbZIP68 could form homodimer and form heterodimer with other members of G group; N-terminal proline rich domain of AtbZIP16 had transactivation activity in yeast cells while that of AtbZIP68 did not; AtbZIP16 and AtbZIP68 GFP fusion protein localized in the nucleus of onion epidermal cells. These results indicated that AtbZIP16 and AtbZIP68 were two new members of GBFs. In Arabidopsis, AtbZIP16 and AtbZIP68 may also participate in light-responsive process in which GBF1-3 are involved.

육용종계와 산란계에서 avian hepatitis E virus의 검출 및 특성 규명 (Detection and characterization of avian hepatitis E virus from broiler breeders and layers in Korea)

  • 문현우;성환우;권혁무
    • 대한수의학회지
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    • 제58권1호
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    • pp.45-49
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    • 2018
  • The helicase genes and hypervariable regions (HVRs) of three avian hepatitis E viruses (HEVs) detected at three different farms were sequenced and characterized. Two isolates (DW-L and GI-B2) were classified as genotype 2 and one isolate (GR-B) was classified as genotype 1. A phylogenetic tree, based on the helicase gene and HVR nucleotide sequences, revealed the newly detected viruses and other avian HEVs were classified similarly. Unlike previously reported avian HEVs, the DW-L isolate detected in broiler breeders with characteristic lesions of avian HEV had no proline-rich motif in its HVR, suggesting that the proline-rich motif is non-essential for viral replication and infection.

A Proline- and Leucine-rich 19 Amino Acid Oligopeptide from FS1 Functions as a Transcriptional Repression Domain

  • Cho, Yong-Seok;Baek. Gum-Hee;Yoon, Sang-Soon;Han, Dong-Uck;Han, Kyu-Hyung
    • Animal cells and systems
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    • 제1권4호
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    • pp.647-651
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    • 1997
  • We have used a transient expression assay employing Drosophila S2 cells to study the transcriptional repression activity of a 27 amino acid residue-long repression domain FS1 which was generated by a frame-shift in a pair-rule gene, even-skipped of Drosophila melanogaster. In an attempt to define a minimal requirement for the repression activity, we constructed a series of truncation mutant forms of the FS1, fused to a heterologous GAL4 DNA-binding domain, and measured their activities. All of the mutant forms, including the GAL4-FS1 (5-23) which retains the smallest number (19) of amino acid residues of FS1, were found to repress an initiator, a minimal TATA-lacking promoter, in a GAL4-binding-site-dependent manner. These findings suggest that a 19 amino acid residue-long region, rich in proline and leucine residues, is a transcriptional repression domain and may interact with the general transcription machinery.

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인체 타액내 당단백질의 구조와 기능 (Structure and Function of Glycoproteins in Human Saliva)

  • Song Han
    • Journal of Oral Medicine and Pain
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    • 제20권1호
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    • pp.19-28
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    • 1995
  • 타액은 구강 환경을 조절하는 여러 가지 유기질과 무기질의 혼합물로 구성되어 있다. 구강 점막은 여러 타액 점액 단백질과 타액 항세균 단백질에 의해서 윤활이 되며 보호된다.타액의 다른 작용은 구강 점막을 축축하게 하고 음식을 부드럽게 한다. 구강건조증은 세균의 침착을 야기시키거나 점막면을 거칠게 하여 출혈이 되기 쉽게 하며 이로 인해 감염이 야기될 수 있다. 이러한 타액의 보호 작용은 mucin, fibronectins, proline-rich glycoproteins, histidine-rich proteins, $\alpha$-amylase, s-IgA 같은 특별한 타액 당단백질에 기인한다고 하는 것이 지난 30년 동안에 알려져 있다. 이러한 분자들의 구조, 구조와 기능사이의 관계, 타액 내 이러한 물질들의 농도에 관한 것들이 알려지고 있는 중이다. 이러한 타액 당단백질 특히 mucin, fibronectin, fucose-rich protein과 s-IgA의 구조와 기능에 대한 현재의 견해들을 이 논문에서 요약하고자 한다.

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굴젓갈 숙성중 글리코겐과 단백질의 분해 (Decomposition of Glycogen and Protein in Pickled Oyster during Fermentation with Salt)

  • 김장양;변재형;남택정
    • 한국수산과학회지
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    • 제14권2호
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    • pp.66-71
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    • 1981
  • 굴의 주요구성분인 글리코겐과 단백질의 굴젓갈 숙성중의 분해과정과 분해생성물 상호간의 관계를 알아보기 위하여, 글리코겐의 분해생성물인 유리환원당과 젓산의 생성 유리아미노산과 단백질 구성아미노산의 젓갈 숙성 전후의 구성변화 및 유리환원당과 유리아미노산간의 첫갈숙성조건에서의 반응성의 지표로서 유효성라이신의 양의변화 등을 분석 검토하였다. 글젓갈 숙성중 글리코겐과 단백질은 분해생성물인 유리환원당과 젓산, 그리고 유리아미노산에로 분해하여 갔으며, 유효성라이신의 양은 미미하게 감소하였다. 단백질을 구성하는 아미노산의 구성을 분석한 결과, 생굴 단백질 구성아미노산중에는 glutamic acid, aspartic acid, lysine, proline이 많았으며, tryptophan과 methionine, histidine 및 tyrosine은 적게 함유되어 있었다. 굴젓갈 단백질 구성아미노산중에는 생굴단백질 구성아미노산중 valine과 histdine isoleucine 및 lysine이 감소된 것이 주목을 끌었다. 유리아미노산의 구성을 보면 생굴중에는 proline, taurine, glycine, glutamic acid, alanine이 특히 함유되어 있었으며, 이들 아미노산의 전체 생굴 유리아미노산에 대한 비율은 약 $69\%$에 달하였다. 그리고 젓갈중에는 proline, glutamic acid, glycine, alanine, aspartic acid 및 lysine이 많이 함유되어 있었으며, 이들 유리아미노산은 전체 굴 젓갈 유리아미노산의 약 $65\%$에 달하였다. 굴젓갈 숙성중에 증가한 유리아미노산은lysine, arginine, aspartic acid, glutamic acid, cysteine, isoleucine, tyrosine등을, 그리고 감소한 아미노산은 taurine, proline, leucine등을 들 수 있었다.

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유자중(柚子中) Amino Acids에 관(關)한 연구(硏究) (Studies on Contents of Amino Acids in Citrus Junos Sieb)

  • 정지흔
    • Applied Biological Chemistry
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    • 제15권2호
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    • pp.175-180
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    • 1972
  • 유자(柚子)의 성분(成分)인 Amino acid의 함유량(含有量)을 구명(究明)하기 위하여 유자(柚子)와 하귤(夏橘)을 각각(各各) 비교(比較) 검토(檢討)하였든 바 다음과 같은 결과(結果)를 얻었기에 이에 보고(報告)하는 바이다. 1 유자(柚子)나 하귤중(夏橘中)에 총(總) Amino acid수(數)는 3종(種), 합(合)하여 20종(種)에 달(達)하였다. 2. 과피율(果皮率)에 유자(柚子)와 하귤(夏橘)의 Amino acid 함유량(含有量)은 전자(前者)에 Proline 16.48mg/100mg, 후자(後者)에는 Aspartic acid 32.68mg/100mg이 각각(各各) 최고(最高)이며 Histidine은 공(共)히 함유량(含有量)이 적었다. 3. 과육중(果肉中)에는 유자(柚子)의 경우 Aspartic acid 32.68mg/100mg, 하귤(夏橋)은 Proline 20.92mg/100mg로 가장 많았고, 전자(前者)에 Histidine 1.32 mg/100mg, 후자(後者)에는 Tyrosine 1.18mg/100mg로 비교적(比較的) 적었다. 4. 유자(柚子)나 하귤중(夏橘中)에는 Amino acid중 일반(一般)으로 Aspartic acid, Proline의 함유량(含有量)이 많다는 것을 알 수 있고 Histidine이 가장 적게 들어 있으며 과육중(果肉中)에는 과피(果皮)보다 각종(各種) Amino acid 함유량(含有量)이 많고 그 중에서도 Glutamic acid가 다른 Amino acid보다 많이 함유(含有)되어 있다.

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인간 타액내 항 린산칼슘 침전 단백질 (Protein Inhibition Precipitation of Calcium Phosphate in Human Saliva)

  • Song Han
    • Journal of Oral Medicine and Pain
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    • 제20권1호
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    • pp.7-18
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    • 1995
  • The Purpose of this article is to describe the biochemical properties and biological functions of several salivary proteins that possess the unusual properties of inhibiting spontaneous and secondary precipitation of calcium phosphate. This function is very important since human salivary secretion is supersaturated with respect to calcium phosphate. Biological function of statherin, proline rich protein (PRP) and histidine rich protein (HRP) is to inhibit precipitation of calcium phosphate in salivary glands, in the oral fluids, and onto tooth surfaces. The resulting supersaturated state of the salivary secretions contributes a protective and reparative environment which is important for the integrity of the tooth. Beneficial consequences of salivary supersaturation with respect to calcium phosphate are selectively expressed in the oral cavity- that is, protection is provided for the dental enamel-while undesirable consequences, for example, precipitation of calcium phosphates in the salivary glands and onto the teeth do not occur. Purification and structural characteristics of these proteins as well as clinical significance of functions of each protein will be discussed.

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