We have previously shown that a Calixarene derivative was an excellent agent for protein immobilization on a solid phase. We further characterized the recognition mechanism between the ‘host’ Calixarene derivative and ‘guest’ molecules in this...

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https://www.riss.kr/link?id=A105874801
Hyun Jeong Kim (Hallym University) ; Sang Wook Oh (Chonbuk National University) ; Sung Joong Kim (Boditech Med Inc.) ; Afsaneh Amiri (Hallym University) ; Hong Tao Wang (Hallym University) ; 최의열 (한림대학교)
2012
English
KCI등재후보,SCOPUS,SCIE
학술저널
1-9(9쪽)
8
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
We have previously shown that a Calixarene derivative was an excellent agent for protein immobilization on a solid phase. We further characterized the recognition mechanism between the ‘host’ Calixarene derivative and ‘guest’ molecules in this...
We have previously shown that a Calixarene derivative was an excellent agent for protein immobilization on a solid phase. We further characterized the recognition mechanism between the ‘host’ Calixarene derivative and ‘guest’ molecules in this study. The rate of complex formation of Calixcrown with amino acids informed that Calixcrown had the strongest interaction with Arg among the tested amino acids. In order to confirm that Arg is an effective residue in immobilization of protein on Calixcrown-coated glass, several human recombinant superoxide dismutase tagged with different numbers of Arg or Lys were generated. The recombinant protein tagged with longer Arg was immobilized better than the ones tagged with shorter Arg or Lys. We also tested if Calixcrown can immobilize oligoDNA as efficiently as it does protein. Calixcrown most strongly captured homo-dGTP oligoDNA among the four homo-oligoDNAs. When Calixcrown chip was applied to detect single nucleotide polymorphism, it differentiated one base pair mismatch of the double helix oligoDNA. Thus, Calixarene derivative linker molecule can be used as an efficient immobilization agent for both protein and oligoDNA with the right orientation on a solid phase.
참고문헌 (Reference)
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7 Schug, K.A., "Noncovalent binding between guanidinium and anionic groups: focus on biological-and synthetic-based arginine/guanidinium interactions with phosphonate and sulfonate residues" 105 : 67-114, 2005
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학술지 이력
| 연월일 | 이력구분 | 이력상세 | 등재구분 |
|---|---|---|---|
| 학술지등록 | 한글명 : BioChip Journal외국어명 : BioChip Journal | ||
| 2023 | 평가 | 해외DB학술지평가 신청대상 (해외등재 학술지 평가) | |
| 2020-01-01 | 등재 | 등재학술지 유지 (해외등재 학술지 평가) | ![]() |
| 2013-10-01 | 등재 | 등재학술지 선정 (기타) | ![]() |
| 2011-01-01 | 등재 | 등재후보 1차 PASS (등재후보1차) | ![]() |
| 2009-01-01 | 등재 | SCIE 등재 (신규평가) | ![]() |
학술지 인용정보
| 기준연도 | WOS-KCI 통합IF(2년) | KCIF(2년) | KCIF(3년) |
|---|---|---|---|
| 2016 | 1.33 | 0.25 | 0.88 |
| KCIF(4년) | KCIF(5년) | 중심성지수(3년) | 즉시성지수 |
| 0.66 | 0.53 | 0.255 | 0.1 |