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Dive into the research topics where Naoko Makita is active.

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Featured researches published by Naoko Makita.


Biophysical Chemistry | 2002

Proton concentration (pH) switches the higher-order structure of DNA in the presence of spermine

Naoko Makita; Kenichi Yoshikawa

Single-chain observations on the conformational change of giant DNA (T4 DNA) molecules were performed using fluorescence microscopy at different values of pH in the presence of spermine. Individual DNA molecules undergo a large discrete change, or all-or-none transition, in conformation from a folded compact state to an unfolded coil state with an increase in pH. This abrupt unfolding of DNA with an increase in pH is attributed to a decrease in the concentration of the tetravalent form in spermine [SPM(4+)]. We propose a scheme for the folding transition of single DNAs, where the manner of spermine binding changes dramatically from weak loose binding in the elongated coil state to strong tight binding in the folded compact state. We discuss the hierarchical nature of the transition, i.e. cooperative continuous change on the ensemble vs. all-or-none switching on individual DNAs.


FEBS Letters | 1999

ATP/ADP switches the higher-order structure of DNA in the presence of spermidine

Naoko Makita; Kenichi Yoshikawa

In the living cellular environment, DNAs exist in a compact state in the presence of a polyamine, such as spermidine. We found that the hydrolysis of ATP into ADP induces the folding of elongated DNAs, by the single‐chain observation of individual T4 DNA molecules. This result is discussed in relation to the possible role of ATP as a regulatory factor in genetic activity, in addition to its well‐established role as an energy source.


Journal of Physical Chemistry B | 2011

Salt Has a Biphasic Effect on the Higher-Order Structure of a DNA−Protamine Complex

Naoko Makita; Yuko Yoshikawa; Yoshiko Takenaka; Takahiro Sakaue; Mari Suzuki; Chika Watanabe; Tamotsu Kanai; Toshio Kanbe; Tadayuki Imanaka; Kenichi Yoshikawa

We observed single DNA molecules by fluorescence microscopy to clarify the effect of protamine on their higher-order structure. With an increase in the protamine concentration, the conformation of DNA molecules changes from an elongated coil state to a compact state through an intermediate state. Furthermore, the long-axis length of DNA gradually decreases while maintaining a distribution profile with a single peak. Such behavior is markedly different from the conformational transition of DNA induced by small polyamines such as spermidine and spermine, where individual DNA molecules exhibit an all-or-none transition from a coil to a globule state and the size distribution is characterized by twin peaks around the transition region. Next, we examined the effect of salt on the conformation of the DNA-protamine complex. Interestingly, at a fixed concentration of protamine, DNA tends to shrink with an increase in the NaCl concentration up to 300 mM, and then swells with a further increase in the NaCl concentration, that is, biphasic behavior is generated depending on the salt concentration. For comparison, we examined the effect of salt on DNA compaction induced by the trivalent polyamine spermidine. We confirmed that salt always has an inhibitory effect on spermine-induced compaction. To clarify this biphasic effect of salt on protamine-induced DNA compaction, we performed a numerical simulation on a negatively charged semiflexible polyelectrolyte in the presence of polycations with relatively large numbers of positive charges by taking into account the effect of salt at different concentrations. The results showed that salt promotes compaction up to a certain concentration and then tends to unfold the polyelectrolyte chain, which reproduced the experimental observation in a semiquantitative manner. This biphasic effect is discussed in relation to the specific shielding effect that depends on the salt concentration.


Journal of Chemical Physics | 2008

Folding transition of a single semiflexible polyelectrolyte chain through toroidal bundling of loop structures

Takafumi Iwaki; Naoko Makita; Kenichi Yoshikawa

We consider how the DNA coil-globule transition progresses via the formation of a toroidal ring structure. We formulate a theoretical model of this transition as a phenomenon in which an unstable single loop generated as a result of thermal fluctuation is stabilized through association with other loops along a polyelectrolyte chain. An essential property of the chain under consideration is that it follows a wormlike chain model. A toroidal bundle of loop structures is characterized by a radius and a winding number. The statistical properties of such a chain are discussed in terms of the free energy as a function of the fraction of unfolded segments. We also present an actual experimental observation of the coil-globule transition of single giant DNA molecules, T4 DNA (165.5 kbp), with spermidine (3+), where intrachain phase segregation appears at a NaCl concentration of more than 10 mM. Both the theory and experiments lead to two important points. First, the transition from a partially folded state to a completely folded state has the characteristics of a continuous transition, while the transition from an unfolded state to a folded state has the characteristics of a first-order phase transition. Second, the appearance of a partially folded structure requires a folded structure to be less densely packed than in the fully folded compact state.


international symposium on micro-nanomechatronics and human science | 2009

Controlling the higher-order structure of DNA-protamine complex

Yuko Yoshikawa; Naoko Makita; Mari Suzuki; Eri Shindo; Chika Watanabe; Tamotsu Kanai; Tadayuki Imanaka; Toshio Kanbe; Kenichi Yoshikawa

We investigated the interaction of large DNA with protamine, a small basic protein, using fluorescence microscopy and electron microscopy. In most vertebrate sperm cells, a large DNA is packaged by protamine into a highly compact, biologically inactive form of chromatin. The manner of packaging plays a key role in spermatogenesis. We found that, with increase of protamine concentration, DNA molecules show the conformational change from an elongated coil state into a compact state through the occurrence of the intermediate state. We also show that the higher-order structure of DNA-protamine complex can be controlled by optical tweezers (Nd YAG laser, 1064 nm) without any structural modification of DNA such as an attachment of plastic beads. These results are discussed in relation to the biological meaning.


Physical Review Letters | 2010

DNA Compaction in a Crowded Environment with Negatively Charged Proteins

Maria K. Krotova; V. V. Vasilevskaya; Naoko Makita; Kenichi Yoshikawa; Alexei R. Khokhlov


Journal of Physical Chemistry Letters | 2010

Compaction of DNA Induced by Like-Charge Protein: Opposite Salt-Effect against the Polymer-Salt-Induced Condensation with Neutral Polymer

Kenichi Yoshikawa; Seiko Hirota; Naoko Makita; Yuko Yoshikawa


Macromolecules | 2006

Conformational change of giant DNA with added salt as revealed by single molecular observation

Naoko Makita; Magnus Ullner; Kenichi Yoshikawa


Biomacromolecules | 2003

NTP concentration switches transcriptional activity by changing the large-scale structure of DNA.

Tatsuo Akitaya; Kanta Tsumoto; Ayako Yamada; Naoko Makita; Koji Kubo; Kenichi Yoshikawa


生物物理 | 2014

3P126 転写調節タンパク質STPRは長鎖DNAを塩基配列非特異的に折り畳む(05B. 核酸:相互作用・複合体,ポスター,第52回日本生物物理学会年会(2014年度))

Tatsuo Akitaya; Naoko Makita; Naomi Tsumura; Hiroyuki Mayama; Norio Hazemoto; Toshio Kanbe; Hideaki Yamaguchi; Koji Kubo; Anatoly Zinchenko; Shizuaki Murata; Kenichi Yoshikawa; Tomoyasu Aizawa; Makoto Demura

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