Rima B K, Martin S J
J Gen Virol. 1979 Jul;44(1):135-44. doi: 10.1099/0022-1317-44-1-135.
Measles virus induces a large polypeptide (L; mol. wt. 180 K), a large glycopolypeptide (H; mol. wt. 80 K), a nucleocapsid associated polypeptide (P; mol. wt. 70 K), a nucleocapsid polypeptide (N; mol. wt. 60 K), a second glycopolypeptide (F0; mol. wt. 60 K), a matrix or membrane polypeptide (M; mol. wt. 37 K) and a small polypeptide (S; mol. wt. 15 K). The second glycopolypeptide (F0) appears to be cleaved in purified measles virus. Defective interfering particles accumulate during passage of measles virus leading to a decrease in the amounts of virus-specific protein synthesized in infected cells. Even in the best preparations of purified measles virus, host proteins are always detected and these become more predominant in preparations with low infectivity.
麻疹病毒可诱导产生一种大分子多肽（L；分子量180K）、一种大的糖多肽（H；分子量80K）、一种与核衣壳相关的多肽（P；分子量70K）、一种核衣壳多肽（N；分子量60K）、第二种糖多肽（F0；分子量60K）、一种基质或膜多肽（M；分子量37K）以及一种小分子多肽（S；分子量15K）。第二种糖多肽（F0）似乎在纯化的麻疹病毒中会被切割。在麻疹病毒传代过程中，缺陷干扰颗粒会积累，导致受感染细胞中合成的病毒特异性蛋白量减少。即使在纯化麻疹病毒的最佳制剂中，也总能检测到宿主蛋白，并且在低感染性的制剂中这些蛋白会变得更加占主导地位。
