WO2017118390A1 - 利用变化电场磁场电磁场有选择地操控分子 - Google Patents

利用变化电场磁场电磁场有选择地操控分子 Download PDF

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WO2017118390A1
WO2017118390A1 PCT/CN2017/070191 CN2017070191W WO2017118390A1 WO 2017118390 A1 WO2017118390 A1 WO 2017118390A1 CN 2017070191 W CN2017070191 W CN 2017070191W WO 2017118390 A1 WO2017118390 A1 WO 2017118390A1
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field
molecule
electric field
selecting
manipulation
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PCT/CN2017/070191
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吴翔
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吴翔
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    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N13/00—Treatment of microorganisms or enzymes with electrical or wave energy, e.g. magnetism, sonic waves

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  • the present invention belongs to the fields of inorganic chemistry, organic chemistry, and biomolecules.
  • DNA, RNA that selectively manipulates a particular base sequence is selected in a biological sample.
  • Molecules include both molecules with unit sequence characteristics and molecules without unit sequence characteristics.
  • the prior art utilizes microwaves to alter the physicochemical properties of molecules.
  • the inventive method highlights the selection of molecules that manipulate sequences of a particular polar unit, or highlights the manipulation of molecules that manipulate a particular structure. When the effect is significant, only the molecules that manipulate the sequence of a particular polar unit are selected, or only the molecules that control a particular structure are selected.
  • All or part of the chain of the chain molecule is elastic.
  • the bases, base pairs, and amino acids in the chain have their own polarity and polarity. It can also be used as a combination of two or more polar parts, including non-polar conditions.
  • An applied electric field acts on a base, a base pair, or an amino acid, and each base, base pair, or amino acid is subjected to a different moment. It includes both polar and non-polar forms.
  • the polar portion is subjected to a moment by a uniform electric field or a non-uniform electric field.
  • the non-polar portion can also be subjected to a moment by arranging the electric field line distribution of the external electric field. Combining the moments of all bases, base pairs, or amino acids, acts on the entire DNA molecule (single or double stranded)
  • RNA molecules single or double stranded
  • protein molecules the moment of RNA molecules (single or double stranded) or protein molecules.
  • An applied electric field acts on a base, a base pair, or an amino acid, and each base, base pair, or amino acid is subjected to a force. It includes both polar and non-polar forms. The polar portion is subjected to a force by a non-uniform electric field. Pass The electric field line distribution of the external electric field is also arranged to force the non-polar portion.
  • the force that combines all bases, base pairs, or amino acids is the force that acts on the entire DNA molecule (single or double stranded), RNA molecules (single or double stranded), or protein molecules.
  • a base, a base pair, or an amino acid in a chain is called a unit. Also included are units of any chain molecule other than a base, a base pair, and an amino acid.
  • the moment of each element at any time includes the torque obtained from the applied electric field and the torque transmitted from the adjacent unit. Starting from any unit, select any direction, and change the applied electric field when the torque change is transmitted to the next unit. On the next unit, the moment is the sum of the two, that is, the moment applied by the external electric field and the moment transmitted by the adjacent unit. The moment that combines all the elements in a segment over a period of time is the moment that acts on the entire segment. A fragment is part of a chain molecule. Depending on the application, the moment acting on the segment can be regarded as the moment acting on the entire chain molecule, and the moment acting on the segment cannot be regarded as the moment acting on the entire chain molecule.
  • the force of each unit at any time includes the force from the applied electric field and the force transmitted from the adjacent unit. Start from any unit, select any direction, and change the force to the next unit. Change the applied electric field.
  • the force is the sum of the two, that is, the force applied by the external electric field and the force transmitted from the adjacent unit.
  • the force that combines all the elements in a segment over a period of time is the force acting on the entire segment.
  • a fragment is part of a chain molecule.
  • the force acting on the segment is considered to be the force acting on the entire chain molecule, and the force acting on the segment cannot be regarded as the force acting on the entire chain molecule.
  • the affected fragment is referred to as the target fragment, and the molecule in which the target fragment is located is referred to as the target molecule.
  • the electric field mode that completely conforms to the sequence of cells is the fundamental electric field mode.
  • a DNA strand which may be a small segment of a DNA molecule present, or a complete DNA molecule
  • the background electric field pattern enables the DNA strand (including the DNA strand) DNA molecules) are constrained in specific directions.
  • the specific direction is not unique.
  • the restriction of the DNA strand is limited by the degree of freedom.
  • the DNA strand is helical and curled, which means that a sufficiently strong background electric field mode can
  • the DNA strand rotates in the direction of its own curl.
  • the curly-shaped DNA strand (including the DNA molecule in which the DNA strand is located) can be restrained in a specific direction.
  • the electric field pattern that constrains the coiled chain molecules in a particular direction is a constrained electric field mode.
  • the curled shape of the DNA molecule is not well known in advance, so the easier mode of operation is the background electric field mode.
  • all chain molecules and fragments thereof have a corresponding background electric field mode and a constrained electric field mode.
  • the target molecule can be screened from a plurality of different sequences of chain molecules by a background electric field mode or a constrained electric field mode.
  • External electric fields show irregular changes to non-target molecules, resulting in irregular movements.
  • the external electric field exhibits congruent, complementary or sequence-like changes to the target molecule.
  • any electric field mode can be superimposed to control the molecular motion. Even the purpose of destroying the target molecule.
  • the DNA fragment is continuously rotated so that it cannot be stretched, that is, a specific gene is locked so that it cannot be copied and expressed.
  • the DNA molecule is suddenly given a sufficiently strong electric field to cause braking during sustained rotation, thereby causing physical fracture.
  • the rotational speed of the DNA molecules is brought to an extreme, thereby contributing to physical rupture.
  • the fragments in the DNA molecule are rotated to accumulate elastic potential energy until physical breakage.
  • the segment in the DNA molecule is rotated, and the natural frequency of the elastic is used to resonate the rotational driving torque with the natural frequency to accumulate the elastic potential energy until physical fracture.
  • DNA molecules move within the force field and accumulate in the local part of the nucleus. DNA molecules have a chance to penetrate the nucleus through the nucleus.
  • DN is normally replicated in living cells with a sequence characteristic. That is, the DNA polymerase performs base pairing one by one. DNA is shown to be single-stranded by the action of helicase. Applying equality and complementation to any link Or a similar field will affect DNA replication. The impact can be both to speed up replication and to slow down and hinder replication.
  • an electromagnetic field acts on a functional group that responds to the electromagnetic field.
  • the functional group belongs to a unit of a chain type molecule. The units are arranged to form a chain molecule.
  • Non-long-chain molecules have their own characteristics of electric field and magnetic field distribution, and the parts (functional groups) that respond to electromagnetic fields also have their own characteristics.
  • the simplest examples are: electric dipole molecules, electric quadrupole molecules, electric octapole molecules, etc., which exhibit different electric field distributions.
  • Magnetic dipole molecules, magnetic quadrupole molecules, magnetic octupole molecules, etc. they exhibit different magnetic field distributions.
  • Fluorescent dyes respond to electromagnetic waves only at functional functional groups. Therefore, the uniformity of the structure, complementarity or similar external field distribution also affects the corresponding molecules.
  • any external field mode can be superimposed to control the molecular motion. Even the purpose of destroying the target molecule.
  • the viral envelope includes a symmetric polyhedron, such as a hepatitis B virus that is a 20-symmetric polyhedron.
  • a symmetric polyhedron such as a hepatitis B virus that is a 20-symmetric polyhedron.
  • Applying a congruent, complementary or similar electric field to a specific polyhedron captures the target molecule. Then, the electric field is superimposed into the rotation mode, which drives the polyhedron to rotate together. And it does not drive other molecules to follow the rotation. If the rotation causes the virus shell to be destroyed, the virus structure is directly destroyed. If the rotation does not destroy, it also interferes with virus replication. Even if the field is static, it interferes with the assembly of the virus casing. Deliberately changing the symmetry of the external field, resulting in the failure of 20-sided polyhedrons to be assembled intact, is also a means of interfering with molecular synthesis.
  • the present invention also includes: treating a disease by a method of manipulating a specific molecule. For example, destroying the DNA, RNA, protein or viral envelope of the corresponding pathogen. It is used to treat hepatitis B, treat malaria, treat AIDS and treat cancer.
  • the content of the invention further includes: processing 0-infinite multiple units per second.
  • the scope of protection is not reduced due to specific molecular species or applications.
  • Processing 10 11 to 10 13 units per second, the corresponding frequency band is in the terahertz range. It is not only based on the propagation speed of elastic transfer manufacturing to determine the speed of the sequence. Also based on the working speed of the enzyme protein The order is fast and slow. Speed is usually not a value, but a range.
  • the invention includes playing differently or simultaneously playing sequences according to a plurality of speeds.
  • the content of the invention further includes: selecting a segment length of 0-infinite multiple units.
  • the scope of protection is not reduced due to specific molecular species or applications.
  • the present invention is distinguished from the prior art in that the law of the electric field, the magnetic field, and the electromagnetic field of the substance to be applied or the spatial distribution follows a specific pattern. These changes or spatial distributions are identical, complementary or similar to those of the polar units within the long-chain molecule, matching the structure of the non-long-chain molecules.
  • the method of the invention highlights the selection of molecules that manipulate sequences of a particular polar unit, or highlights the manipulation of molecules that manipulate a particular structure.
  • a significant embodiment of the invention is implemented when the effect is significant, i.e., only molecules that manipulate a particular sequence of polar units are selected, or only molecules that manipulate a particular structure are selected.
  • a set of doughs that are continuously affected by the electric field sequence, and the sequence corresponding to the yeast DNA is an electric field sequence. Named Group B.
  • a set of doughs that are continuously affected by the electric field sequence, with an optional non-yeast sequence as an electric field sequence Named Group C.
  • the electric field sequences of the 8 and C groups should be designed so that the two electric field sequences are input to the same power as the experimental object.
  • the subject can be observed at any time until the difference is seen.
  • Group C was compared with Group A, and the greater significance of the dough of Group C was that the electric field sequence produced a slight thermal effect. Accelerate fermentation.
  • Group B is compared with Group C, and the smaller meaning of the dough of Group B is that the electric field sequence of the yeast DNA sequence will affect Fermentation. Promote fermentation slowdown.
  • Group B is compared with Group A, and the smaller of the dough of Group B is that the electric field sequence of the yeast DNA sequence affects fermentation. Even slower than not doing any electric field effects.
  • a sample of the oil-water mixture is placed in a cup, and the mixture in the cup can be an emulsion to which a surfactant is added.
  • An external electric field is applied to the mixture, and the external electric field is characterized by: an electric field strength increases from the top of the cup toward the bottom of the cup; and a horizontal electric pole exhibits a symmetric electric quadrupole.
  • the oil-water mixture changes from a uniform distribution to an oily bottom, and the water quality rises.
  • an electric field is used.
  • the use of magnetic fields and electromagnetic fields is a simple replacement.
  • the matters not repeated in the examples are set forth in the distinguishing background and the summary of the invention. Because the background technology and the invention content are simple and easy to distinguish, the background technology and the invention content are specific implementation schemes.
  • the external electric field is static.
  • the use of dynamic electric fields in other situations is a simple replacement. Turning an electric field into a magnetic field and an electromagnetic field is a simple replacement.
  • the matters not repeated in the examples are set forth in the distinguishing background and the summary of the invention. Because the background technology and the inventive content are simple and easy to distinguish, the background technology and the invention are different embodiments.
  • the present invention has a significant role in the field of biology and in the medical field. It also brings new ideas to chemical synthesis and material screening.

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Abstract

一种选择操控分子的方法。利用外部电场、磁场或电磁场的分布或者变化给予分子力矩或力，或干涉分子的合成或分解。外场的变化与链型分子内部单元的序列全等、互补或相似，或者外场的分布与分子结构匹配。在此基础上叠加进任何外场模式来控制分子运动。

Description

说明书 发明名称:利用变化电场磁场电磁场有选择地操控分子 技术领域
[0001] 本发明属于无机化学、 有机化学、 生物分子领域。 例如， 在生物样本里有选择 地操控特定碱基序列的 DNA、 RNA。 有选择地操控肽链及蛋白质分子等等。 分 子既包括具有单元序列特点的分子， 也包括没有单元序列特点的分子。
背景技术
[0002] 已有技术利用微波改变分子的物理化学性质。 也有技术利用静电场、 稳恒磁场 和脉冲电场、 脉冲磁场改变分子的物理化学性质。
技术问题
[0003] 发明技术方法突出选择操控特定极性单元序列的分子， 或者突出选择操控特定 结构的分子。 当效果显著吋， 即只选择操控特定极性单元序列的分子， 或者只 选择操控特定结构的分子。
问题的解决方案
技术解决方案
[0004] 针对长链分子， 非长链分子分别探讨。
[0005] 1、 长链分子类：
[0006] 链型分子的全部或局部链条带有弹性。 比如 DNA链、 RNA链及肽链带有弹性
。 链上碱基、 碱基对和氨基酸都有各自的极性和极性大小。 包括非极性情况在 内也能当作两个及两个以上的极性部分拼接而成。
[0007] 外加电场作用于碱基、 碱基对或氨基酸， 每个碱基、 碱基对或氨基酸受到不同 的力矩。 包括极性、 非极性两种形式。 通过均匀电场或非均匀电场能使极性部 分受到力矩。 通过安排外电场的电场线分布也能使非极性部分受到力矩。 综合 所有碱基、 碱基对或氨基酸的力矩， 就是作用于整个 DNA分子 （单链或双链）
、 RNA分子 （单链或双链） 或蛋白质分子的力矩。
[0008] 外加电场作用于碱基、 碱基对或氨基酸， 每个碱基、 碱基对或氨基酸受到力的 作用。 包括极性、 非极性两种形式。 通过非均匀电场能使极性部分受到力。 通 过安排外电场的电场线分布也能使非极性部分受到力。 综合所有碱基、 碱基对 或氨基酸的力， 就是作用于整个 DNA分子 （单链或双链） 、 RNA分子 （单链或 双链） 或蛋白质分子的力。
[0009] 为了叙述方便， 把链上碱基、 碱基对或氨基酸叫做单元。 还包括除了碱基、 碱 基对和氨基酸以外的任何链型分子的单元。
[0010] 因为分子链有弹性， 所以每个单元的力矩变化都会向相邻单元传递。 传递带有 延吋。 每个单元在任何吋候的力矩包括从外加电场得到的力矩和相邻单元传递 来的力矩。 从任意一个单元幵始， 选择任意一个方向， 当力矩变化传递到下一 个单元吋改变外加电场。 在所述下一个单元上， 力矩是两者之合， 即外电场施 予的力矩和相邻单元传递来的力矩之合。 综合一个片段内所有单元在一段吋间 内的力矩， 就是作用于整个片段的力矩。 片段是链型分子的一部分。 根据应用 场合， 有吋把作用于片段的力矩能看作是作用于整个链型分子的力矩， 有吋不 能把作用于片段的力矩看作是作用于整个链型分子的力矩。
[0011] 因为分子链有弹性， 所以每个单元的力的变化都会向相邻单元传递。 传递带有 延吋。 每个单元在任何吋候的力包括从外加电场得到的力和相邻单元传递来的 力。 从任意一个单元幵始， 选择任意一个方向， 当力的变化传递到下一个单元 吋改变外加电场。 在所述下一个单元上， 力是两者之合， 即外电场施予的力和 相邻单元传递来的力之合。 综合一个片段内所有单元在一段吋间内的力， 就是 作用于整个片段的力。 片段是链型分子的一部分。 根据应用场合， 有吋把作用 于片段的力看作是作用于整个链型分子的力， 有吋不能把作用于片段的力看作 是作用于整个链型分子的力。
[0012] 对于一种特定序列的 DNA链、 RNA链及肽链而言， 只有外电场变化规律与序 列全等、 互补或相似， 才会体现出这一种链条受到变化的外电场影响。 为了叙 述方便， 把受影响的片段称作目标片段， 把目标片段所在的分子称作目标分子
[0013] 为了叙述方便， 约定完全顺应单元序列的电场模式为本底电场模式。 例如， 假 使某 DNA链 （可以是存在于中 DNA分子的一小段， 也可以是完整 DNA分子） 是 长直未卷曲的平坦梯子形状， 则本底电场模式能使该 DNA链 （包括 DNA链所在 DNA分子） 约束在特定方向。 特定方向并非唯一的。 DNA链被约束就是被限制 了自由度。
[0014] 然而， DNA链是螺旋形状和卷曲形状的， 这意味着足够强的本底电场模式能使
DNA链顺延自身卷曲方向旋转。
[0015] 显然， 使外电场随着 DNA链旋转的反方向旋转， 就能使卷曲形状的 DNA链 ( 包括 DNA链所在 DNA分子） 约束在特定方向。 为了叙述方便， 约定能使卷曲的 链型分子约束在特定方向的电场模式为约束电场模式。 DNA分子的卷曲形状并 不能很好地预先知道， 因此更容易操作的模式是本底电场模式。
[0016] 除例子所述 DNA分子和 DNA链以外， 所有链型分子及其片段都有对应本底电 场模式和约束电场模式。
[0017] 通过本底电场模式或者约束电场模式， 就能够从众多不同序列的链型分子中筛 选出目标分子。 外电场对于非目标分子而言， 体现出无规律的变化， 促成无规 律的运动。 外电场对于目标分子而言， 体现出全等、 互补或相似于序列的变化
， 并能约束目标分子的运动。
[0018] 通过以上两种电场模式筛选并抓住了目标分子， 就能叠加进任何电场模式来控 制分子运动。 甚至达到破坏目标分子的目的。
[0019] 例如， 使 DNA片段持续地旋转使其无法展幵， 即锁定了某一特定基因使其无法 复制和表达。
[0020] 又例如， 使 DNA分子在持续的旋转中突然给予足够强的电场促成制动， 从而促 成物理断裂。 或者， 使 DNA分子的旋转速度达到极限， 从而促成物理断裂。 或 者， 针对 DNA分子中的片段进行旋转， 积累弹性势能， 直至物理断裂。 或者， 针对 DNA分子中的片段进行旋转， 并利用弹性制造的固有频率， 使旋转的驱动 力矩与固有频率共振， 积累弹性势能， 直至物理断裂。
[0021] 又例如， 使 DNA分子在力场内移动， 聚集在细胞核的局部。 DNA分子有几率 通过核孔穿出细胞核。
[0022] 除了利用弹性操控链型分子外。 还有其它具有吋序的特征能被利用。 例如， D NA在活细胞内正常复制吋带有吋序特征。 即 DNA聚合酶一个接一个地进行碱基 配对。 DNA在解旋酶作用下展幵为单链。 针对任何一个环节， 施加全等、 互补 或者相似的外场， 都会影响 DNA复制。 影响既能够是加快复制， 又能够是减缓 、 阻碍复制。
[0023] 除了用电场工作外， 还能用磁场工作， 磁场作用于具有磁极排列的链型分子。
[0024] 除了用电场、 磁场工作外， 还能用电磁场工作。 例如， 电磁场作用于响应电磁 场的官能团。 所述官能团属于链型分子的单元。 单元排列组成链型分子。
[0025] 2、 非长链分子类：
[0026] 非长链分子对外显现的电场、 磁场分布有各自特征， 响应电磁场的部位 （官能 团） 也有各自特征。 最简单的例子有： 电偶极分子、 电四极分子、 电八极分子 等等， 它们对外显现的电场分布不一样。 磁偶极分子、 磁四极分子、 磁八极分 子等等， 它们对外显现的磁场分布不一样。 荧光染料只在功能官能团部位响应 电磁波。 因此， 结构全等、 互补或者相似的外场分布也区别影响对应分子。
[0027] 通过外场结构筛选并抓住了目标分子， 就能叠加进任何外场模式来控制分子运 动。 甚至达到破坏目标分子的目的。
[0028] 除了能够带动目标分子旋转， 也能够产生作用力导致目标分子位移。
[0029] 除了能够带动目标分子运动， 还能够干涉目标分子的合成或分解。
[0030] 例如， 病毒外壳包括对称多面体， 如乙肝病毒是 20面对称多面体。 针对具体一 种多面体， 施加全等、 互补或者相似的电场， 就抓住了目标分子。 再为电场叠 加进旋转的模式， 就带动了多面体一起旋转。 而且不会带动其它分子跟随旋转 。 若旋转致使病毒外壳被破坏， 则直接破坏病毒结构。 若旋转不致破坏， 也干 扰了病毒复制。 即使外场是静态的， 也干扰了病毒外壳的组装。 有意改变外场 的对称性， 致使 20面多面体总不能完好的拼装， 也是一种干扰分子合成的手段
[0031] 本发明的内容还包括： 利用操控特定分子的方法治疗疾病。 例如破坏对应病原 体的 DNA、 RNA、 蛋白质或病毒外壳。 用来治疗乙肝疾病、 治疗疟疾、 治疗艾 滋病和治疗癌症等等。
[0032] 本发明的内容还包括： 每秒处理 0-无穷多个单元。 不因具体的分子种类或应用 场合而缩小保护范围。 每秒处理 10 11到 10 13个单元， 对应频段在太赫兹范围。 不 仅仅依据弹性传递制造的传播速度来决定吋序快慢。 还依据酶蛋白工作速度决 定吋序快慢。 速度通常不是一个值， 而是一个范围。 发明包括依据多个速度不 同吋播放或同吋播放序列。
[0033] 本发明的内容还包括： 选用片段长度是 0-无穷多个单元。 不因具体的分子种类 或应用场合而缩小保护范围。
发明的有益效果
有益效果
[0034] 本发明区别于现有技术， 在于施予物质的电场、 磁场、 电磁场的变化规律或空 间分布遵循特定模式。 这些变化规律或空间分布与长链分子内部极性单元的序 列全等、 互补或者相似， 与非长链分子的结构匹配。 发明技术方法突出选择操 控特定极性单元序列的分子， 或者突出选择操控特定结构的分子。 当效果显著 吋， 即只选择操控特定极性单元序列的分子， 或者只选择操控特定结构的分子 实施该发明的最佳实施例
本发明的最佳实施方式
[0035] 1、 利用酵母菌在发面中的效果做对比， 验证本发明的作用。
[0036] 一组不做任何电场影响的发面团。 定名 A组。
[0037] 一组受电场序列持续影响的发面团， 以酵母 DNA对应的序列为电场序列。 定名 B组。
[0038] 一组受电场序列持续影响的发面团， 以任选非酵母菌的序列为电场序列。 定名 C组。
[0039] 特别地， 我们注意到应该设计好8、 C两组的电场序列， 使两种电场序列输入 给实验对象的功率一样。
[0040] 以上三组实验对象在现场的环境温度下同期进行发酵。 初期， 发面团都是等大 的。
[0041] 任何吋候能够观察实验对象， 直至看出差别。
[0042] C组与 A组对照， C组的面团更大的意义在于电场序列会产生轻微热作用。 促 成发酵加速。
[0043] B组与 C组对照， B组的面团更小的意义在于酵母 DNA序列的电场序列会影响 发酵。 促成发酵减速。
[0044] B组与 A组对照， B组的面团更小的意义在于酵母 DNA序列的电场序列会影响发 酵。 甚至比不做任何电场影响还慢。
[0045] 此对比实验中， 把 DNA单侧链条上的 C和 T编码为 0， G和 A编码为 1。 0信号和 1 信号代表电场方向互为相反。 这不是唯一的编码方法， 也不代表发明对编码方 法的限制。
[0046] 此对比实验中， 采用每秒处理 500-1500个碱基对的速率， 并且在速率范围内扫 频。 这个值不是最佳速率范围。 这个值不代表发明的限定范围。
[0047] 此对比实验中， 采用本底电场模式。
[0048] 此对比实验中， 采用 500个碱基对， 朝一个方向播放电场序列到数据末尾后立 即倒转序列方向播放， 或者从头顺序播放。 过程循环往复。 500个碱基对不是最 佳数值， 也不代表发明的限定范围。
[0049] 此对比实验中， 实验结果不排除 B组在电场刺激下加速发酵比 C组更快， 结果 B 组的面团比 C组的更大。 B组 C组有区别即验证发明的作用。 不论结论是抑制发 酵还是促进发酵。
[0050] 2、 油水混合物分离
[0051] 虽然选择操控极性的水分子比选择操控非极性的油分子更容易， 但是为了在实 施例中突出发明作用， 选择操控非极性的油分子。
[0052] 把油水混合物样品置于杯中， 杯中混合物能够是添加了表面活性剂的乳液。
[0053] 针对混合物施加外电场， 外电场的特征是： 从杯顶向杯底方向电场强度增加； 水平面方向呈现对称的电四极。
[0054] 油水混合物从均匀分布变为油质沉底， 水质上浮。
本发明的实施方式
[0055] 最佳实施方式 1项中， 使用的是电场。 在其它场合采用磁场、 电磁场属于简单 替换。 实施例中未重复的事项均在区别背景技术及发明内容中陈述。 因为区别 背景技术及发明内容简单易行， 故区别背景技术及发明内容就是具体实施方案 [0056] 最佳实施方式 2项中， 外电场是静态的。 在其它场合采用动态的电场属于简单 替换。 把电场变为磁场、 电磁场属于简单替换。 实施例中未重复的事项均在区 别背景技术及发明内容中陈述。 因为区别背景技术及发明内容简单易行， 故区 别背景技术及发明内容就是具体实施方案。
工业实用性
[0057] 能够预见， 本发明在生物学领域， 医疗领域具有明显的作用。 也给化工合成， 物质筛选带来崭新的思路。

Claims

权利要求书
一种选择操控分子的方法， 其特征是： 利用外部电场、 磁场或电磁场 的变化给予链型分子力矩或力， 或干涉链型分子的合成或分解， 外部 电场、 磁场或电磁场的变化与链型分子内部单元的序列全等、 互补或 相似， 所述单元具备电极或磁极， 或能够响应电磁波。
根据权利要求 1所述选择操控分子的方法， 其特征是： 夕卜部电场、 磁 场或电磁场的变化模式包含本底外场模式或者约束外场模式。
根据权利要求 2所述选择操控分子的方法， 其特征是： 在所述本底外 场模式或者约束外场模式基础上叠加进任何外场模式来控制分子运动
一种选择操控分子的方法， 其特征是： 利用外部电场、 磁场或电磁场 的分布给予分子力矩或力， 外部电场、 磁场或电磁场的分布与分子结 构匹配。
根据权利要求 4所述选择操控分子的方法， 其特征是： 在所述匹配的 外场基础上叠加进任何外场模式来控制分子运动。
根据权利要求 1-5之一所述选择操控分子的方法， 其特征是： 分子能 够是 DNA分子、 RNA分子、 肽链、 蛋白质或病毒外壳。
根据权利要求 1-5之一所述选择操控分子的方法， 其特征是： 破坏病 原体的 DNA、 RNA、 蛋白质或病毒外壳， 或者促进 DNA、 RNA或蛋 白质的合成及表达， 或者阻碍 DNA、 RNA或蛋白质的合成及表达。 根据权利要求 1-3之一所述选择操控分子的方法， 其特征是： 每秒处 理 0-无穷多个单元， 速度能够是一个值， 也能够是一个范围， 依据多 个速度不同吋播放或同吋播放序列。
根据权利要求 1-3之一所述选择操控分子的方法， 其特征是： 选用片 段长度是 0-无穷多个单元。
根据权利要求 8所述选择操控分子的方法， 其特征是： 每秒处理 10 11 到 10 13个单元， 对应频段在太赫兹范围。
PCT/CN2017/070191 2016-01-05 2017-01-04 利用变化电场磁场电磁场有选择地操控分子 WO2017118390A1 (zh)

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