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| MALDI-TOF× | Circular Dichroism× | |
|---|---|---|
| 분야 | 분광학 | 분광학 |
| 계열 | Process / pipeline | Process / pipeline |
| 기원 연도≠ | 1988 | 1969 |
| 창시자≠ | Michael Karas | Jean-Claude Fasman |
| 유형≠ | Ionization and mass analysis technique | Spectroscopic method |
| 원전≠ | Karas, M., & Hillenkamp, F. (1988). Laser desorption ionization of proteins with molecular masses exceeding 10,000 daltons. Analytical Chemistry, 60(20), 2299-2301. DOI ↗ | Greenfield, N. J., & Fasman, G. D. (1969). Computed circular dichroism spectra for protein secondary structures. Biochemistry, 8(10), 4108-4116. DOI ↗ |
| 별칭 | MALDI mass spectrometry, MALDI-TOF-MS, laser desorption mass spectrometry | CD spectroscopy, circular dichroism, CD analysis |
| 관련 | 3 | 3 |
| 요약≠ | Matrix-Assisted Laser Desorption/Ionization (MALDI) combined with Time-of-Flight (TOF) mass analysis, or MALDI-TOF, is a soft ionization mass spectrometry technique that gently ionizes intact biomolecules and volatile organic compounds, then measures their mass-to-charge ratio by measuring flight time through a field-free drift region. Introduced independently by Karas, Hillenkamp, and Tanaka in 1988, MALDI-TOF revolutionized proteomics, microbiology, and organic analysis by enabling mass determination of proteins and polymers exceeding 100 kDa. | Circular Dichroism (CD) spectroscopy measures the differential absorption of left- and right-circularly polarized light by optically active molecules, particularly proteins and nucleic acids. Introduced by Greenfield and Fasman in 1969, CD is a rapid, non-destructive technique for characterizing secondary structure (alpha-helix, beta-sheet), monitoring protein folding transitions, and assessing conformational changes in response to pH, temperature, or ligand binding. |
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