JPH06183400A - Protein crystal growing device - Google Patents
Protein crystal growing deviceInfo
- Publication number
- JPH06183400A JPH06183400A JP4337016A JP33701692A JPH06183400A JP H06183400 A JPH06183400 A JP H06183400A JP 4337016 A JP4337016 A JP 4337016A JP 33701692 A JP33701692 A JP 33701692A JP H06183400 A JPH06183400 A JP H06183400A
- Authority
- JP
- Japan
- Prior art keywords
- protein
- container
- protein solution
- crystal
- solution
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Crystals, And After-Treatments Of Crystals (AREA)
- Peptides Or Proteins (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はタンパク質結晶成長装置
に関し、特に無重力空間で利用可能な同装置に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a protein crystal growth apparatus, and more particularly to the apparatus that can be used in a weightless space.
【0002】[0002]
【従来の技術】従来のタンパク質結晶成長装置を図3に
よって説明する。図3において、01はタンパク質溶液
容器、02は析出剤溶液容器、03はバルブである。タ
ンパク質溶液容器01、析出剤溶液容器02は共に内径
10mm程度のものであり、中央のバルブ03を反時計
方向に90°回転させることにより左側の析出剤溶液容
器02の析出剤溶液と右側のタンパク質溶液容器01の
タンパク質溶液が接触し、タンパク質結晶が成長する方
式のものである。なお、図3中、Bはタンパク質溶液と
析出剤溶液との接触界面を示す。2. Description of the Related Art A conventional protein crystal growth apparatus will be described with reference to FIG. In FIG. 3, 01 is a protein solution container, 02 is a precipitant solution container, and 03 is a valve. Both the protein solution container 01 and the precipitant solution container 02 have an inner diameter of about 10 mm, and by rotating the central valve 03 counterclockwise by 90 °, the precipitant solution in the left precipitant solution container 02 and the right protein can be This is a system in which the protein solution in the solution container 01 contacts and the protein crystals grow. In FIG. 3, B indicates the contact interface between the protein solution and the precipitant solution.
【0003】[0003]
【発明が解決しようとする課題】従来のタンパク質結晶
成長装置では図3に示す左側の析出剤溶液と、右側のタ
ンパク質溶液との間で、液々界面での拡散を利用するも
のであるが、容器の容積が大きいためタンパク質試料を
大量に準備する必要があり、また形成される結晶の固定
が困難であり、しかもX線照射による構造解析のために
X線回折用キャピラリ(均一薄肉ガラスの内径1mm程
度の毛細管)に移し変える作業を要する等問題点があ
る。The conventional protein crystal growth apparatus utilizes diffusion at the liquid-liquid interface between the precipitant solution on the left side and the protein solution on the right side shown in FIG. Since the volume of the container is large, it is necessary to prepare a large amount of protein samples, and it is difficult to fix the crystals that are formed. In addition, for structural analysis by X-ray irradiation, an X-ray diffraction capillary (inner diameter of uniform thin glass) There is a problem in that it needs to be transferred to a capillary tube of about 1 mm).
【0004】このうち、結晶の固定が不充分であると、
結晶がタンパク質溶液の中を移動して、相互に接触する
可能性が増大する。結晶の接触は、単結晶性を損ねた
り、甚だしい場合には一旦成長した結晶を損傷する結果
を産むが、これらの悪い結果は、ことに無重力空間で成
長させたタンパク質結晶を地上に回収する際に問題とな
る。また、キャピラリに移し変える作業も、同様に、結
晶に歪みを与えて単結晶性を損ねたり、結晶を損傷した
りする危険を伴うという問題をもつ。本発明は上記技術
水準に鑑み、従来のタンパク質結晶成長装置の有する上
述したような問題点のないタンパク質結晶成長装置を提
供しようとするものである。Of these, if the fixation of crystals is insufficient,
Crystals move through the protein solution, increasing the likelihood of contacting each other. The contact of crystals results in the loss of single crystallinity and, in extreme cases, damage to crystals once grown, but these bad results are especially caused when the protein crystals grown in weightless space are collected on the ground. Will be a problem. Further, the work of transferring to a capillary also has a problem that strain is applied to the crystal to impair the single crystallinity, or the crystal is damaged. In view of the above-mentioned state of the art, the present invention aims to provide a protein crystal growth apparatus that does not have the above-mentioned problems that the conventional protein crystal growth apparatus has.
【0005】[0005]
【課題を解決するための手段】本発明はタンパク質溶液
と析出剤溶液とを接触させ、その界面での析出剤の拡散
によりタンパク質結晶を成長させる装置において、タン
パク質溶液を複数の均一薄肉なガラス毛細管より構成し
てなることを特徴とするタンパク質結晶成長装置であ
る。The present invention relates to a device for contacting a protein solution with a precipitant solution and growing a protein crystal by diffusing the precipitant at the interface, wherein the protein solution is provided with a plurality of uniformly thin glass capillaries. It is a protein crystal growth apparatus characterized by comprising the following.
【0006】[0006]
【作用】タンパク質結晶成長装置のタンパク溶液容器と
して、内径1mm程度の均一薄肉ガラス毛細管を採用す
ることにより、結晶形成後、結晶が大きな距離を移動す
る可能性がなくなり、更に、該容器を取り出すのみで、
そのままX線照射による構造解析が可能となる。また、
タンパク溶液容器を内径1mm程度の複数の均一薄肉ガ
ラス毛細管にしたため、必要なタンパク質溶液液量が少
くてよく、貴重なタンパク質試料に対応できる。更に、
この種の装置の原理である液々界面での拡散は均一薄肉
ガラス毛細管の小さな断面積ではなく、バルブ内の広い
断面積で行なわれるため、拡散の界面面積は減少するこ
とはないが、一方で結晶成長が実際に起こる部分の断面
積ははるかに減少するために、内部で熱対流が抑えら
れ、拡散律速の条件下で良質の結晶が成長し、かつ温度
制御に対する応答性がよい。なお、本発明で使用する析
出剤溶液としては塩溶液、水溶性高分子溶液、水溶性有
機溶媒溶液が一般的に使用される。[Function] By adopting a uniform thin-walled glass capillary tube having an inner diameter of about 1 mm as a protein solution container of a protein crystal growth apparatus, there is no possibility that the crystal will move a large distance after the crystal is formed, and only the container is taken out. so,
The structure analysis by X-ray irradiation can be performed as it is. Also,
Since the protein solution container is made of a plurality of uniform thin glass capillaries having an inner diameter of about 1 mm, the required amount of the solution of the protein solution is small, and it can be used for a valuable protein sample. Furthermore,
Diffusion at the liquid-liquid interface, which is the principle of this type of device, is performed not by a small cross-sectional area of a uniform thin glass capillary tube but by a wide cross-sectional area in the bulb, so that the diffusion interface area does not decrease. Since the cross-sectional area of the part where the crystal growth actually occurs is much reduced, the thermal convection is suppressed inside, a good quality crystal grows under the diffusion-controlled condition, and the response to the temperature control is good. A salt solution, a water-soluble polymer solution, and a water-soluble organic solvent solution are generally used as the precipitant solution used in the present invention.
【0007】[0007]
【実施例】以下、本発明のタンパク質結晶成長装置の一
実施例を図1、図2によって説明する。図1はその縦断
側面図、図2は図1の一部拡大図である。図1、図2に
おいて、1はタンパク質溶液容器、2は析出剤溶液容
器、3はバルブ、4は各容器保持部を示す。EXAMPLE An example of the protein crystal growth apparatus of the present invention will be described below with reference to FIGS. 1 is a vertical sectional side view thereof, and FIG. 2 is a partially enlarged view of FIG. In FIGS. 1 and 2, 1 is a protein solution container, 2 is a precipitant solution container, 3 is a valve, and 4 is a container holder.
【0008】本発明の実施例装置により拡散した析出剤
溶液の析出剤分子は拡散とタンパク質溶液容器1の毛細
管力によりタンパク質溶液容器1に導入され、該容器1
内でタンパク質結晶を析出する。かくして、本発明実施
例装置によればタンパク質溶液容器1を取出すことによ
り、直ちにX線照射によるタンパク質結晶の構造解析を
行なうことができる。The precipitant molecules of the precipitant solution diffused by the apparatus of the present invention are introduced into the protein solution container 1 by diffusion and the capillary force of the protein solution container 1, and the container 1
Protein crystals are precipitated in the. Thus, according to the apparatus of the present invention, by taking out the protein solution container 1, it is possible to immediately perform the structural analysis of the protein crystal by X-ray irradiation.
【0009】更に本発明の実施例装置においては、バル
ブ3を図1に示すように設置しておくと、タンパク質溶
液はバルブ3内に充填されているので、バルブ3を90
°回転させると析出剤溶液とタンパク質溶液とはバルブ
3内のAで接触し界面を生ずる。これに対し、図3に示
した従来の装置のバルブ03の位置ではバルブ03の回
転により両溶液の接触界面は図3のバルブ03のBの位
置である。勿論、本発明の実施例装置においても、バル
ブ3の向きを180°反対にしておけばバルブ3に析出
剤溶液が充填され、接触界面は図3と同様にBになり、
タンパク質試料が貴重で多量に準備できない事態にも対
応することができる。Further, in the apparatus of the embodiment of the present invention, when the valve 3 is installed as shown in FIG. 1, since the protein solution is filled in the valve 3, the valve 3 is set to 90 °.
When rotated by °, the precipitant solution and the protein solution come into contact with each other at A in the valve 3 to form an interface. On the other hand, at the position of the valve 03 in the conventional apparatus shown in FIG. 3, the contact interface between both solutions is at the position B of the valve 03 in FIG. 3 due to the rotation of the valve 03. Of course, also in the apparatus of the embodiment of the present invention, if the direction of the valve 3 is reversed by 180 °, the valve 3 is filled with the depositing agent solution, and the contact interface becomes B as in FIG.
It is possible to deal with the situation where a large amount of protein samples are rarely prepared.
【0010】[0010]
【発明の効果】本発明によれば、タンパク質溶液が少量
でよく、タンパク質溶液容器が毛細管であるため、析出
したタンパク質結晶の固定が可能である。また、タンパ
ク質溶液容器を均一の薄肉ガラス毛細管としたので、タ
ンパク質溶液容器を保持部より取出すだけで、そのまま
X線回折用キャピラリとして流用することができる効果
も奏する。EFFECTS OF THE INVENTION According to the present invention, a small amount of protein solution is sufficient, and the protein solution container is a capillary tube, so that the precipitated protein crystals can be fixed. Further, since the protein solution container is a uniform thin glass capillary tube, it is possible to use the protein solution container as it is as an X-ray diffraction capillary simply by taking it out from the holding portion.
【図1】本発明の一実施例のタンパク質結晶成長装置の
縦断側面図。FIG. 1 is a vertical side view of a protein crystal growth apparatus according to an embodiment of the present invention.
【図2】図1の一部拡大図。FIG. 2 is a partially enlarged view of FIG.
【図3】従来のタンパク質結晶成長装置の一態様の縦断
側面図。FIG. 3 is a vertical sectional side view of one embodiment of a conventional protein crystal growth apparatus.
───────────────────────────────────────────────────── フロントページの続き (72)発明者 加藤 真樹 兵庫県神戸市兵庫区和田崎町1丁目1番1 号 三菱重工業株式会社神戸造船所内 (72)発明者 深山 春生 兵庫県神戸市兵庫区和田崎町1丁目1番1 号 三菱重工業株式会社神戸造船所内 ─────────────────────────────────────────────────── ─── Continued Front Page (72) Inventor Maki Kato 1-1-1, Wadasaki-cho, Hyogo-ku, Kobe-shi, Hyogo Mitsubishi Heavy Industries, Ltd. Kobe Shipyard (72) Inventor Haruyama Miyama, Hyogo-ku, Kobe-shi, Hyogo 1-1-1 Tasakicho Mitsubishi Heavy Industries Ltd. Kobe Shipyard
Claims (1)
せ、その界面での析出剤の拡散によりタンパク質結晶を
成長させる装置において、タンパク質溶液容器を複数の
均一薄肉なガラス毛細管より構成してなることを特徴と
するタンパク質結晶成長装置。1. A device for growing a protein crystal by contacting a protein solution with a precipitant solution and diffusing the precipitant at the interface, wherein the protein solution container comprises a plurality of uniformly thin glass capillaries. A protein crystal growth apparatus characterized by:
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33701692A JP3357906B2 (en) | 1992-12-17 | 1992-12-17 | Protein crystal growth equipment |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33701692A JP3357906B2 (en) | 1992-12-17 | 1992-12-17 | Protein crystal growth equipment |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH06183400A true JPH06183400A (en) | 1994-07-05 |
JP3357906B2 JP3357906B2 (en) | 2002-12-16 |
Family
ID=18304676
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP33701692A Expired - Lifetime JP3357906B2 (en) | 1992-12-17 | 1992-12-17 | Protein crystal growth equipment |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3357906B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011011947A (en) * | 2009-07-02 | 2011-01-20 | Japan Atomic Energy Agency | Method and apparatus for growing large-scale crystal of biomolecule |
-
1992
- 1992-12-17 JP JP33701692A patent/JP3357906B2/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011011947A (en) * | 2009-07-02 | 2011-01-20 | Japan Atomic Energy Agency | Method and apparatus for growing large-scale crystal of biomolecule |
Also Published As
Publication number | Publication date |
---|---|
JP3357906B2 (en) | 2002-12-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EXPY | Cancellation because of completion of term |