首页> 外国专利> End of aids for general virology, based on profound science as protein foldings: safe vaccines, universal antimicrobial means, mad cow end

End of aids for general virology, based on profound science as protein foldings: safe vaccines, universal antimicrobial means, mad cow end

机译:以深入的科学作为蛋白质折叠的基础为普通病毒学提供辅助手段的方法:安全疫苗,通用抗菌手段,疯牛病

摘要

All AIDS principal mysteries are resolved. “One step” AIDS is successive contaminations.(with low [anti-env]). Strong sole lethal animal doses are confirming. Mobility macrophage (mφ) receptors contaminate at 1st stage with nonproductive entry with nonintegrated and heterogenous (due to nef) HIV DNA and proteins and preudoinfectious A particles. Such heterogeneity is obligatory for 2nd productive contamination with heterogenous anti-env, with integrated DNA and homologous proteins. Encephalites are due to moving into brain myp due to locally liberated cyto and chemokines Nongenetic factors are determining: at general persistent seronegativity (contact regularity) or absence of 2nd contamination due to different Fc receptor carbohydrates (babies before 3 months, chimpanzee). Minor genetic factors (as CCR5-2) only modify. AIDS in explaining all dangerous vaccinations. Carbohydrate origin of NK-cell mechanism. Artificial. virus culture contaminations. HIV signallings are resolved with general laws of functional recognitions and foldings with help of Universalest “Du-2T”-like peptides and 2 prolyl-isomerases (coupled trans-cis transitions). Chaperons protect proteins against intercarbohydrate aggregations. Prione “scarpie” state is artificial dissociation of their “Du-2T”. MHC and TRC allbtypes are due to their carbohydrates. Hearts of any cell functionning: “PKC” transporting vesicle cycle and independent direct DNA activation. Apoptosis: irreversibility of preparation of next signal with stock exhaustions. Ribosome cycles. Key proprotein primary structures confirm above data. Consequences of profoundest bases: mφ mobility stopping against encephalites; charged antibodies eliminate viruses, cancer cells and harmful antibody clones (anti-viral ,anti-auto); “Du-2T” eliminates viruses and “Mad Cow”; vaccines from homogenous viruses with one neutralizing epitope and correct virus titres; ribosomal protein synthesis; means against clinical death and coma; perfectest hypnotics.
机译:艾滋病的所有主要奥秘都得到解决。艾滋病的“一步”是连续的污染([抗env]低)。强大的唯一致命动物剂量正在证实。流动性巨噬细胞(mφ)受体在第一阶段受到污染,因为非生产性进入而与非整合性和异源性(由于nef感染)HIV DNA和蛋白质以及伪感染性A颗粒污染。这种异质性对于异源抗env,整合的DNA和同源蛋白的第二次生产性污染是必须的。脑炎是由于局部释放的细胞和趋化因子而转移到脑部息肉中的。非遗传因素正在确定:一般持续的血清阴性(接触规律)或由于不同的Fc受体碳水化合物(3个月前的婴儿,黑猩猩)而没有第二次污染。次要遗传因素(如CCR5-2)仅会改变。艾滋病解释所有危险的疫苗接种。 NK细胞机制的碳水化合物起源。人工的。病毒培养物污染。 HIV信号传导通过功能识别和折叠的通用法则得到解决,这是通用的“ Du-2T”样肽和2个脯氨酰异构酶(耦合的顺式-顺式转变)的帮助。分子伴侣保护蛋白质免受碳水化合物间的聚集。 Prione的“ scarpie”状态是其“ Du-2T”的人工离解。 MHC和TRC的allbtypes是由于它们的碳水化合物。任何细胞功能的心脏:“ PKC”转运囊泡周期和独立的直接DNA激活。凋亡:备料耗尽时下一信号的制备不可逆。核糖体周期。关键的前蛋白一级结构证实了以上数据。最深厚的基础的后果:mφ迁移阻止脑水;带电抗体消除病毒,癌细胞和有害抗体克隆(抗病毒,抗自体); “ Du-2T”消除病毒,“ Mad Cow”消除;具有一种中和表位和正确病毒滴度的均质病毒疫苗;核糖体蛋白合成;防止临床死亡和昏迷的手段;最完美的催眠药。

著录项

  • 公开/公告号US2005130125A1

    专利类型

  • 公开/公告日2005-06-16

    原文格式PDF

  • 申请/专利权人 YULY ZAGYANSKY;

    申请/专利号US20040505353

  • 发明设计人 YULY ZAGYANSKY;

    申请日2002-03-04

  • 分类号C12Q1/70;

  • 国家 US

  • 入库时间 2022-08-21 22:25:40

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