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04. Proteins:Determination
BIOMEDICAL IMPORTANCE
PROTEINS & PEPTIDES MUST BE PURIFIEDPRIOR TO ANALYSIS
Column Chromatography
- 藉由column中beads的物理化學性質,將通過的溶液篩出想要的東西
HPLC—High-Pressure Liquid Chromatography
- 第一代column chromatography的beads很大顆(0.1 mm),flow的效果較差。而總表面積小,限制了添加charged or ligand-like groups
- 進化的column的beads較細,但阻力變大,因此需要高壓。高壓會把原本由多醣體製成的beads壓碎,後來有silicon beads才克服
Size-Exclusion Chromatography
-
根據蛋白質的Stokes radii來做篩選
- Stokes radii為蛋白質的effective volume occupied,與mass及shape有關
- Size越小,越易先陷入beads的凹洞,因此越往下size越大
Ion-Exchange Chromatography
- Beads可做成陽離子及陰離子
Hydrophobic Interaction Chromatography
- Stationary phase用hydrophobic group做coating
Affinity Chromatography
- 用ligands
Protein Purity Is Assessed by Polyacrylamide Gel Electrophoresis (PAGE)
- SDS-PAGE
- SDS = sodium dodecyl sulfate,為陰離子清潔劑。每一個SDS結合兩個peptide bonds,使polypeptide展開或變性,因此可將蛋白質解開,之後再跑電泳
Isoelectric Focusing (IEF)
- 蛋白質因為電性移動到環境pH等於其isoelectric point (pI)之處
- IFE-SDS-PAGE:兩個向量(平面),一個根據電荷質量比做電泳,另一個則根據pI做電泳
SANGER WAS THE FIRST TO DETERMINE THE SEQUENCE OF A POLYPEPTIDE
- 胰島素
- 1-fluoro-2,4-dinitrobenzene為Sanger's reagent,會和α-amino groups反應,等於是把peptide的α端的胺基酸做標記,因而可知是哪一個胺基酸
THE EDMAN REACTION ENABLES PEPTIDES & PROTEINS TO BE SEQUENCED
- Phenyl isothiocyanate為Edman reagent,也可標記α端的胺基酸。與Sanger's reagent不同,此反應可逆,也就是試劑可反覆使用(同一試劑依序定序出胺基酸)
- 很費工夫,因為要先把蛋白切成許多peptides,然後要靠重疊的部份去判斷出整段的順序
MOLECULAR BIOLOGY REVOLUTIONIZED THE DETERMINATION OF PRIMARY STRUCTURE
- DNA sequencing比定序胺基酸更有效率
GENOMICS ENABLES PROTEINS TO BE IDENTIFIED FROM SMALL AMOUNTS OF SEQUENCE DATA
- Edman technique已被mass spectrometry (MS)取代做為辨認蛋白的工具
MASS SPECTROMETRY CAN DETECT COVALENT MODIFICATIONS
- 可辨視出posttranslational modification
MASS SPECTROMETERS COME IN VARIOUS CONFIGURATIONS
Peptides Can Be Volatilized for Analysis by Electrospray Ionization or Matrix-Assisted Laser Desorption
Tandem Mass Spectrometry
- 縮寫:MS-MS或MS2
- 篩檢新生兒代謝性疾病
PROTEOMICS & THE PROTEOME
The Goal of Proteomics Is to Identify the Entire Complement of Proteins Elaborated by a Cell Under Diverse Conditions
Simultaneous Determination of Hundreds of Proteins Is Technically Challenging
- 第一代proteomics用SDS-PAGE或two-dimensional電泳,再用Edman技術去辨視蛋白