Patent Grant
12241886
This application is a U.S. National Phase Application of PCT/CN2018/073716, filed Jan. 23, 2018, which claims priority to CN 201710060033.9, filed Jan. 24, 2017, the contents of which applications are incorporated herein by reference in their entireties for all purposes.
Incorporated herein by reference in its entirety is a Sequence Listing named “C127820052 SequenceListing”, which is being submitted to the USPTO via EFS-web on even date herewith as an ASCII text file 24.8 KB in size. This file, which was created on Jul. 21, 2019, constitutes both the paper and computer readable form of the Sequence Listing.
This invention belongs to the field of biotechnology, in particular to a transmembrane nanopore with nucleic acid unwinding function and its construction method and application.
Accurately detection of biological and chemical active substances is one of the targets of industry and scientific research through ages, which requires robust and stable sensors. Since the first application of α-hemolysin (α-HL) in the field of single molecule detection, nanopores, as a technical platform for single molecule detection, have been playing an increasingly important role.
Binding or “capturing” the interested analytes for detection via intermolecular affinity interactions (e.g. covalent binding or noncovalent attraction), for example, specifically distinguish and quantify the divalent metal ions such as nickel, copper, and zinc by inserting histidine into the (3-barrel district of α-HL; small organic molecules and even fractions of proteins can be detected by embedding specific ligands into inner nanopores through gene engineering, amino acid configurations can also be differentiated via combining copper ion with cysteine (117) of α-HL nanopore.
Besides α-HL, other researched protein nanopores contains alamethicin-used for detection of polyethylene glycol, Mycobacterium smegmatis recombinant protein MspA-widely used for high throughput nucleic acid sequencing at present, bacteriophage phi29 DNA packaged motor protein-allowing double strands to pass by, etc. The nanopore of these proteins, such as α-HL and MspA, requires other enzymes for assists to complete the detection of analytes, which limits its further application.
From the existing research reports, when the α-HL nanopore, which with the narrowest diameter of 1.5 nm in the transmembrane (3-barrel district and the length of 5.2 nm, was used for sequencing or sensing of other small molecules, the length at the narrowest part of nanopore was too long to make the nucleic acid chain ratchet through the nanopore, as a result, it was difficult to distinguish single base, and the sensing resolution of other small molecules was therefore reduced.
Though the length of the transmembrane section of MspA is shorter than α-HL, it is usually only functioned as a nanopore, being equal to an artificial carbon nanotubes in sensing molecular, and existing as an ion channel. For example, Ian M, Elizabeth, etc. coupled Hel308 helicase or Φ129DNA polymerase with MspA to distinguish single base in nucleic acid.
The electrical signal from phi29 DNA packaged motor protein is easily interfered, when it detects trace substances, attributing to its poor voltage-gated characteristics.
Those skilled in the art are using other materials, such as synthetic metal or silicon nanopore, for potential application of sequencing, however, these synthetic nanopores are not reliable enough to produce consistent repetitive structures and lack diversity in chemical modification. Therefore, searching for better nanopores or their substitutions is still a hotspot and difficulty in this field.
The technical problem to be solved in the invention is to overcome the deficiency of the existing protein nanopore with small channel size which needs to externally unwind active components when transferring double-stranded nucleic acid.
This invention provides a monomeric protein to solve the deficiency mentioned above. The monomeric protein, (1) being consisted of amino acids from 306 to 577 position of isolated bovine papillomavirus double-strand DNA helicase, and its sequence is shown in SEQ ID No. 3, Or (2) being a variant obtained by substitution and/or deletion and/or insertion of at least one amino acid in the amino acid sequence of the protein defined in (1).
Furthermore, the monomeric protein in this invention is a variant obtained by substituting and/or deleting and/or inserting 1 to 20 amino acids in the amino acid sequence of the protein defined in (1).
Optimally, it is a variant obtained by substituting and/or deleting and/or inserting 1 to 15 amino acids in the amino acid sequence of the protein defined in (1).
Further, the above-mentioned protein is a variant obtained by substituting and/or deleting and/or inserting no more than 10 amino acids in the amino acid sequence of the protein defined in (1), owning the same or similar function with the monomeric protein.
Preferably, a restricted variant with (1) obtained by substituting and/or missing and/or inserting 1 to 10 amino groups in the amino acid sequence of the protein shown in (1).
Preferably, a restricted variant with (1) obtained by substituting and/or missing and/or inserting 1 to 5 amino groups in the amino acid sequence of the protein shown in (1).
Preferably, a restricted variant with (1) obtained by substituting and/or missing and/or inserting 1 to 3 amino groups in the amino acid sequence of the protein shown in (1).
Further, the above protein variant is the protein variant obtained from K mutation to L at 421, or from H mutation to W at 323 of the protein with amino acid sequence SEQ ID No. 3.
Preferred: The above protein variant is a homologous variant, which has more than amino acid sequence homology of 75% with the sequence of SEQ ID No. 3 as defined in (1).
Preferred: The above protein variant is a homologous variant, which has more than amino acid sequence homology of 80% with the sequence of SEQ ID No. 3 as defined in (1).
More preferred: The above protein variant is a homologous variant, which has more than amino acid sequence homology of 90% with the sequence of SEQ ID No. 3 as defined in (1).
Re-optimization: The above protein variant is a homologous variant, which has more than amino acid sequence homology of 95% with the sequence of SEQ ID No. 3 as defined in (1).
Further optimization: The above protein variant is a homologous variant, which has more than amino acid sequence homology of 98% with the sequence of SEQ ID No. 3 as defined in (1).
Optimal: The above protein variant is a homologous variant, which has more than amino acid sequence homology of 99% with the sequence of SEQ ID No. 3 as defined in (1).
The present invention also provides genes encoding the above-mentioned proteins.
Further, the nucleotide sequence of the above genes is shown in SEQ ID No. 4.
At the same time, the invention also provides vectors containing the above genes.
Of course, the present invention also provides host cells containing the above vectors.
The invention also provides another protein, (1) being consisted of amino acids from 306 to 605 position of isolated bovine papillomavirus double-strand DNA helicase, its sequence is shown in SEQ ID No. 1; or (2): being a variant obtained by substitution and/or deletion and/or insertion of at least one amino acid in the amino acid sequence of the protein defined in (1).
Further, the monomer protein is a variant obtained by substituting and/or deleting and/or inserting of 1 to 20 amino acids in the amino acid sequence of the defined in (1).
Preferably, the monomer protein is a variant obtained by substituting and/or deleting and/or inserting 1 to 15 amino acids in the amino acid sequence of the protein defined in (1).
Further, the above proteins are protein with the same or similar function as that of the monomer protein obtained by substituting and/or deleting and/or inserting no more than 10 amino acids in the amino acid sequence of the protein defined in (1).
Preferably, the monomer protein is a variant obtained by substituting and/or deleting and/or inserting 1 to 10 amino acids in the amino acid sequence of the protein defined in (1).
Re-optimally, the monomer protein is a variant obtained by substituting and/or deleting and/or inserting 1 to 5 amino acids in the amino acid sequence of the protein defined in (1).
More optimally, the monomer protein is a variant obtained by substituting and/or deleting and/or inserting 1 to 3 amino acids in the amino acid sequence of the protein defined in (1).
Preferred: the above protein variant is a homologous variant, which has more than amino acid sequence homology of 75% with sequence of SEQ ID No. 1 as defined in (1).
Preferred: the above protein variant is a homologous variant, which has more than amino acid sequence homology of 80% with sequence of SEQ ID No. 1 as defined in (1).
More optimally, the above protein variant is a homologous variant, which has more than amino acid sequence homology of 90% with sequence of SEQ ID No. 1 as defined in (1).
Re-optimally, the above protein variant is a homologous variant, which has more than amino acid sequence homology of 95% with sequence of SEQ ID No. 1 as defined in (1).
Further preferably, the above protein variant is a homologous variant, which has more than amino acid sequence homology of 98% with sequence of SEQ ID No. 1 as defined in (1).
Most preferably, the above protein variant is a homologous variant, which has more than amino acid sequence homology of 99% with sequence of SEQ ID No. 1 as defined in (1).
Further, the above protein is the protein variant obtained from K mutation to L at 421, or from H mutation to W at 323 of the protein with amino acid sequence shown in SEQ ID No. 1.
Further, the amino acid sequences of the protein variants are shown in SEQ ID No. 6 and SEQ ID No. 7 respectively.
The present invention also provides genes encoding the above-mentioned protein.
Further, the nucleotide sequences of the above genes are shown in SEQ ID No. 2.
The invention also provides a coding gene of the protein variant. The nucleotide sequence is shown in SEQ ID No. 8 and SEQ ID No. 9 respectively.
At the same time, the invention also provides a vector containing the above genes.
Of course, the present invention also provides host cells containing the above vector.
In addition, the invention also provides a polymer protein. The polymer protein contains more than two of the above-mentioned protein as subunits.
Furthermore, the number of subunits constituting the multimeric protein is 4-8.
Preferably, the number of subunits constituting the multimeric protein is 6.
Wherein, the above-mentioned polymer proteins are homomultimer or heteropolymer.
The invention also provides a use of the above-mentioned protein or polymer protein in the preparation of nanopore or membrane containing conductive pores.
The invention also provides a membrane containing conductive pores, it comprises: (1) a membrane layer; and (2) a separated above-mentioned polymer protein, which is embedded in the membrane layer to form a pore which can be electrically conducted through the pore when a transmembrane potential is applied.
Wherein, the membrane layer in the nanopore comprises a lipid layer.
Wherein, the lipid layer in the nanopore contains amphiphilic lipids.
Wherein, the lipid layer in the nanopore can be a planar membrane layer or a liposome.
Further, when the nanopore is applied potential, the conductive pore membrane can translocate DNA or RNA through the pore.
Preferably, the monolayer described in the above-mentioned membrane layer is formed by PMOXA-PDMS-PMOXA, PMOXA is dimethyl-diazolin, and PDMS is polydimethylsiloxane.
In addition, the invention also provides a method for preparing a membrane containing conductive pores, which is characterized by the following steps:
(a) Preparing dried amphiphilic lipids;
And (b) resuspending the dried amphiphilic lipids in a solution comprising aqueous solvent, penetrating agent and several separated proteins mentioned above, the protein as subunits can be self-assembled into hexamer protein, which can insert into lipid bilayer membrane under certain conditions and sufficient time to form a membrane containing conductive pore. Preferably, the polymer protein is a hexamer.
Wherein, the amphiphilic lipids mentioned above are phospholipids.
Wherein, the phospholipids mentioned above is selected from one or more of the phospholipids listed below: phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine serine, phosphatidylinositol, phosphatidylglycerol, cardiolipid, 1,2-diphytyl-sn-glycerol-3-phosphatidylcholine, and 1,2-diphenyl-sn-glycerol-3-phosphatidylcholine.
The invention also provides a use of nanopore in the preparation of single-molecule sensor or kits.
The invention also provides a single molecule sensor or a reagent kit, which contains the nanopore as one of the components.
The invention also provides an application of bovine papillomavirus double-stranded DNA helicase protein or its homologous protein in preparation of nanopore or membrane containing conductive pore. The amino acid sequence of the bovine papillomavirus double-stranded DNA helicase protein is shown in SEQ ID No. 5. Further, the homologous proteins of the bovine papillomavirus double-stranded DNA helicase protein are selected from table 1 below.
The invention also provides a membrane containing conductive pores, includes: (1) a membrane layer;
And (2) a separated bovine papillomavirus double-stranded DNA helicase protein or its homologous protein, the multimeric protein is embedded in the membrane layer to form pore, which can be electrically conducted when a bias voltage is applied, the amino acid sequence of the double-stranded DNA helicase protein of bovine papillomavirus is shown in SEQ ID No. 5
The homologous protein of the bovine papillomavirus double-stranded DNA helicase protein is selected from table 1.
The key component protein in the mammalian pathogenic virus was modified firstly by protein engineering technology in this invention, so that it can be used to construct a novel protein nanopore for the sensing research of nucleic acid and other substances. The invention expresses and purifies the protein in vitro by prokaryotic expression system, and simultaneously embeds it on the artificial phospholipid bilayer membrane and the polymer membrane to become a protein nanopore. By studying its conductance distribution under various conductivity buffer systems, as well as the transport of single-stranded DNA and single-stranded RNA, and its helicase activity, a novel nanopore sensing system combining the characteristics of porin and the helicase activity of proteins was constructed firstly, and the untwisting and translocation of double-stranded DNA with a single arm was realized on the lipid bilayer.
The beneficial effects of the invention are as follows:
The present invention finds that the bovine papillomavirus double-stranded DNA helicase protein and its homologous protein can be used to prepare a membrane containing conductive pore, it provides a new effective choice for this field.
The present invention discovers the E1-1 (306-577) protein innovatively, which forms a polymer acting as a new and simple membranes containing conductive pore, and we verified it can be stable presence on phospholipid double-layered membranes and it has the characteristics of translocation nucleic acids.
The invention further discovers the new protein E1-2 (306-605), and successfully constructs a nanopore and helicase integrated sensing system based on it, which replaces the existing sensing method that needs to couple the helicase and the nanopore, and it can be used as a biosensor. Compared with the current phi29 and MspA, Hel308 and MspA, and the coupled sensing systems of phi29 and α-HL, the nanopore of the present invention can realize the single enzyme to complete the capture of analytes to be measured, through the pore, which greatly simplify the steps. In particular, the nanopore can simultaneously perform unwinding of double-stranded DNA and analysis of sensing, analysis of nucleic acid polymorphism, analysis of nucleic acid secondary structure, analysis of nucleic acid length, etc. In terms of medicinal use, its potential-driven solute translocation can also be applied to liposome drug delivery therapy (e.g. drug targeted delivery), which has great potential for application.
The invention further carries out mutation research on the molecular basis of the E1-2 protein, and obtains a mutant of the E1-2 protein. The pores formed by the mutant E1-1 (306-577) monomer or E1-2 (306-605) monomer on the artificial lipid membrane have many advantages over the wild type. Specifically, the pores constructed from the mutant monomers are more likely to capture nucleic acids and other small molecules with negatively charged than the wild type. In addition, the pores constructed from the mutant monomers exhibit an increase in current range, which makes the lumen of the pores narrower than that of the wild type, thereby making the pore detection current more extensive and sensitive.
The invention is described in conjunction with the drawings below.
The object of the invention is initiated by a hexamer cyclic helicase of bovine papillomavirus, which plays a role of assisting genomic DNA replication in bovine papillomavirus. Wild-type protein is an ATP-dependent helicase of bovine papillomavirus that exists for melting DNA of a double-helix during viral replication. It is reported that the protein binds to single-stranded DNA and attaches to the genomic DNA replication initiation site in a hexamer form at the initiation of viral genome replication. And under the condition of energy provided by atpase hydrolysis of ATP, it continues to melt along the single-stranded DNA from the replication fork in the 3′-5′ direction.
The full-length protein amino acid sequence (SEQ ID No. 5) of wild-type bovine papillomavirus double-strand DNA helicase E1, has 605 amino acids in total. The italicized and underlined part is E1-1 (306-577):
atnsqakhvkdcatmvrhylraetqalsmpayikarcklatgegswksil
tffnyqniehtitfinalklwlkgipkknclafigppntgksmlcnslih
flggsvlsfanhkshfwlasladtraaliddathacwryfdtylrnaldg
ypvsidrkhkaavqikappllvtsnidvqaedrylylhsrvqtfrfeqpc
tdesgeqpfnitdadwksffvrlwgrldl
ideeedseedgdsmrtftcsa
The invention discovers that the bovine papillomavirus double-stranded DNA helicase protein and its homologous protein can be used to prepare nanopores and membranes containing conductive pore. The prepared nanopore and the membrane containing conductive pore can be used for the preparation of a single molecule sensor or kit for characterizing a target sample. It provides a new and effective choice for the field.
The optional information of the bovine papillomavirus double-stranded DNA helicase protein is shown in table 2 below:
From the crystal structure and functional domain of the protein, we know that the conservative region of the protein is distributed in amino acids 1-121 and amino acids 166-575. In the two conservative regions, amino acids 407-557 are SF3 helicase functional domains, 413-457 amino acids belong to the AAA+ family of ATP hydrolases, and 142-308 amino acids are DNA binding domains. The amino acids 84-86 and 105-108 are respectively nucleic acid positioning signal regions; we identified some of the homologous proteins of these proteins, which have similar structures and same function (unwinding double-stranded DNA under the action of ATP hydrolysis energy). It is expected that these homologous proteins will also form stable pores on the artificial lipid membrane after adopting the described mutation and have the same on-membrane nucleic acid unwinding function as E1-1 (306-577), becoming a tool for the sensing of nucleic acid and small molecules.
According to the crystal structure analysis, the main helical functional domain of bovine papillomavirus double-stranded DNA helicase protein exists in the 308-577 amino acid segment. The invention constructs and purifies E1's truncated polypeptide E1-1 (306-577) in vitro. Using short-chained double-stranded DNA (dsDNA), the activity of ATP-dependent helicase in its hexamer is verified under specific conditions in vitro.
The invention further utilizes the truncated polypeptide E1-1 (306-577) to prepare nanopores. As mentioned in this invention, the hexameric pore completes the translocation of ssDNA, and the probability of translocation of single-stranded DNA (ssDNA) is slightly different.
The invention obtains another truncated body E1-2 (306-605) of E1 in further research. The protein can successfully form a stable nanopores on artificial lipid membrane under various conductive buffer conditions in vitro.
The invention also studies the following nucleic acid sensing using patch-clamp technology. Structural analysis shows that the inner diameter of the nanopore formed by E1-2 protein is about 1.3 nm, and the length of membrane region and the diameter of opening of the protein are about 3.2 nm and 15 nm respectively.
The experiment shown that under the buffer conditions of 1M, 0.3 mM KCl, and PBS, E1 (306-605) can self-assemble into a hexamer on an artificial lipid membrane and firmly form a pore on the membrane. After applying the transmembrane voltage on both sides of the membrane, generates a current passing through the pore. In the subsequent ssDNA transport experiment, it is found that short-chained ssDNA can trigger a series of current blocking phenomena, but using dsDNA to repeat the same experiment does not cause similar phenomena. The transmembrane current is stable, and these phenomena are consistent with the diameter of E1. The diameter of dsDNA is about 2 nm, while the inner diameter limit of E1 is about 1.3 nm, so when the dsDNA with flat end is driven by the transmembrane voltage, it is captured by E1. In most cases, either a continuously blocking with a blockage of more than 50% of the pore or the immediate opening of the pore after blocking occurs; When dsDNA with a single arm is captured by E1 driven by transmembrane voltage in PBS buffer or buffer with equal salt concentration as PBS, a specific concentration of ATP and Mg2+ are added. Combined with E1's own helicase activity and its characteristics as a biological nanopore, it is shown that the double chain unwinding on the artificial lipid membrane was completed in vitro using the pore formed by E1-2 (306-605).
The mutants of E1-1 (306-577) and E1-2 (306-605) also have the same or similar functions and are also within the scope of protection of the invention.
It was found in the study that the mutants of E1-1 (306-577) and E1-2 (306-605) exhibited improved properties for subsequent nanopore incorporation and capture of negatively charged nucleic acids and ssDNA translocation. Specifically, the mutants show surprisingly easier artificial liposome insertion characteristics, stable presence on lipid membranes, and non-specific current fluctuations are further reduced due to the improvement of signal-to-noise ratio of open current caused by the pore. The capture efficiency of ssDNA at the C end of the pore was further improved. In the process of nucleic acid translocation, the inherent force of the pore cavity on ssDNA is weakened, and the translocation current presents a more rapid and regular peak pattern. Another advantage of the mutant is that the mutation does not affect the characteristics of the pore itself as a DNA helicase.
Therefore, the invention provides a mutated E1-1 (306-577) monomer or a mutated E1-2 (306-605) monomer, which contains variants of the amino acid sequence shown in SEQ ID NO.1 or SEQ ID NO.3. Wherein the variant contains at least one of the following mutations (the number of bits of each of the following mutation sites is calculated from the first position of the total length of bovine papilloma virus double-stranded DNA helicase. The total length amino acid sequence of bovine papilloma virus double-stranded DNA helicase is shown in SEQID No. 5):
(a) The amino acid at 479 position is histidine (H), lysine (K), serine (S), asparagine (N), threonine (T);
(b) The amino acid at 489 position is histidine (H), lysine (K), asparagine (N), threonine (T) and serine (S);
(c) The amino acid at 530 position is histidine (H), lysine (K), serine (S), asparagine (N), threonine (T);
(d) The amino acid at 529 position is glutamine (Q) and lysine (K);
(e) The amino acid at 525 position is histidine (H), lysine (K), serine (S), leucine (L), threonine (T);
(f) The amino acid at 504 position is asparagine (N), lysine (K), arginine (R), serine (S), threonine (T), phenylalanine (f), tyrosine (Y), tryptophan (W);
(g) The amino acid at 328 position is glutamine (Q), lysine (K), arginine (R), phenylalanine (F), tyrosine (Y), tryptophan (W);
(h) The amino acid at 360 position is asparagine (N), lysine (K), arginine (R), phenylalanine (F), tyrosine (Y), tryptophan (W);
(i) The amino acid at 322 position is asparagine (N), leucine (L), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), glutamine (Q);
(j) The amino acid at 372 position is glutamine (Q), leucine (L), isoleucine (I), valine (V), proline (P), phenylalanine (F), tryptophan (W), asparagine (N);
(k) The amino acid at 342 position is asparagine (N), leucine (L), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), glutamine (Q);
(l) The amino acid at 334 position is asparagine (N), leucine (l), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), glutamine (Q);
(m) The amino acid at 392 position is asparagine (N), leucine (L), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), glutamine (Q);
(n) The amino acid at 408 position is asparagine (N), leucine (L), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), glutamine (Q);
(o) The amino acid at 396 position is leucine (L), isoleucine (I), valine (V), phenylalanine (F) and tryptophan (W). Alanine (A) and glycine (G);
(p) The amino acid at 570 position is valine (V), phenylalanine (F), tryptophan (W), alanine (A), glycine (G), leucine (L), isoleucine (I);
(q) The amino acid at 574 position is tryptophan (W), alanine (A), glycine (G), leucine (L), isoleucine (I), valine (V) and phenylalanine (F);
(r) The amino acid at 417 position is leucine (L), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), alanine (A) and glycine (G);
(s) The amino acid at 421 position is Valine (V), phenylalanine (F), tryptophan (W), alanine (A), glycine (G), leucine (L) and isoleucine (I);
(t) The amino acid at 383 position is valine (V), phenylalanine (F), tryptophan (W), alanine (A), glycine (G), leucine (L), isoleucine (I);
(u) The amino acid at 387 position is histidine (H), phenylalanine (F), tryptophan (W);
(v) The amino acid at 323 position is leucine (L), isoleucine (I), valine (v), phenylalanine (F), tryptophan (W), alanine (A), glycine (G).
(w) The amino acid at 324 position is leucine (L), isoleucine (I), proline (P) and valine (V);
(x) The amino acid at 565 position is threonine (T), serine (S) and tyrosine (Y);
(y) The amino acid at 426 position is leucine (L), isoleucine (I), valine (V), phenylalanine (F), tryptophan (W), alanine (A), glycine (G).
The invention provides a mutated E1-1 (306-577) monomer or a mutated E1-2 (306-605) monomer. The above-mentioned E1-1 (306-577) variants or E1-2 (306-605) variant monomers can be used to form the conductive membrane pore in this invention. Mutated E1-1 (306-577) monomer or E1-2 (306-605) monomer is a monomer whose sequence is different from that of wild E1-1 (306-577) monomer or E1-2 (306-605) monomer and retains the ability of forming pore. The methods used to confirm the capability of mutant monomers to form pores are consistent with methods mentioned in this invention.
The mutant E1-1 (306-577) monomer or E1-2 (306-605) monomer has multiple advantages over a wild type monomer in forming a pore on artificial lipid membrane. Specifically, the pore constructed by mutated monomer is more likely to capture nucleic acids and other negatively charged small molecules than wild type, in addition it shows an increase in current range, making the inner cavity of the pore narrower than that of wild type, so that the current detection in the pore is more extensive and sensitive.
In addition, when the mutated E1-1 (306-577) or E1-2 (306-605) monomers form a pore on an artificial lipid membrane, the transmembrane region of the pore is more likely to stably exist on the membrane and the signal-to-noise ratio of open current is higher than that of wild type. Surprisingly, when nucleic acid moves through some pores constructed by mutated E1-1 (306-577) or E1-2 (306-605) monomers, the current decreases even more. This makes it possible to use this pore to identify the relationship between nucleic acid sequence and the current descent platform when the nucleic acid moves through the pore, and further makes this mutant pore have the potential to apply to nucleic acid sequencing in the future. The improvements of nucleic acid reading properties of the mutants are realized through three main mechanisms, namely through changing:
Either or more of these three mechanisms may be the reason why the pore of the invention has nucleotide reading property in the future.
The site mutation of the protein in the invention is mainly based on the following reasons:
In wild type E1-1 (306-577) or E1-2 (306-605), the N terminal is open at the narrower end, the C terminal is open at the wider end, and the hexamer forms a standard mushroom structure. A large number of alkaline amino acids are distributed in the inner cavity of the forming pore, which binds with negative phosphate group of ssDNA. Therefore, When the wild type E1-1 (306-577) or E1-2 (306-605) monomer is inserted into the artificial lipid membrane to form an conducting pore through which ions can freely pass it was found that the pore would fall from the lipid membrane at a long period of applied transmembrane voltage. The recorded open current baseline fluctuated, and small non-specific peak current is appeared occasionally when no molecule to be measured passes through the pore.
We use mutated E1-1 (306-577) or E1-2 (306-605) monomer to improve the above defects. For example, some acidic amino acids at the wider C terminal like aspartic acid (D) at 479 and 489 are mutated to histidine (H) or lysine (K) to increase the capture efficiency of negatively charged nucleic acid at the C terminal of the pore. When mutated to asparagine (N), the density of negatively charged amino acids at C-terminal opening decreased, and the electrostatic antagonism to nucleic acids (mainly) or negatively charged substances to be measured is correspondingly reduced, which indirectly increases the capture rate of the pore.
Another example is that we mutate some acidic amino acids in the pore cavity such as aspartic acid (D) at 504, glutamate (E) at 328, to asparagine (N), lysine (K), arginine (R), Glutamine (Q), etc. Mutating acidic amino acids (D, E) to neutral amino acids, on the one hand, can significantly reduce the electrostatic antagonism during nucleic acid translocation, on the other hand, When the neutral amino acid is phenylalanine (F), tryptophan (W), or tyrosine (Y) with a large steric hindrance, due to the larger spatial position within the formed cavity, the diameter of the non-restricted site in the cavity is significantly reduced. At the same time, when the density of benzene ring inside the substituted cavity increases, π electrons accumulate to make amino acids align more closely and the internal contraction of the cavity is obvious. Of course, these two reductions are double-edged swords in detection. When the neutral amino acid is a hydroxyl group, such as serine (S) or threonine (T), because hydroxyl oxygen can bond with nucleotides by forming hydrogen, the nucleic acid is able to enter the cavity from the C terminal to translocate more slowly. This mechanism will have more beneficial value in the subsequent development of nucleic acid sequencing.
Mutating aspartic acid (D) at 322, 342, 334, glutamate (E) at 372, lysine (K) at 396, 383, histidine (H) at 323 and arginine (R) at 574 in the transmembrane region to neutral amino acid Leucine (L), Glycine (G), alanine (A), etc. enable transmembrane region of the pore more easily and stably embed in the hydrophobic layer of lipid bilayer composed of long fatty acid chains, thus greatly weaken the open current baseline fluctuations and low frequency noise caused by instability of pore inserting. The specific mutation site is shown in table 3 below.
The present invention is further elaborated by embodiments as follows.
The entire bovine papillomavirus genome is amplified using the above PCR primers (as described above), and then the vector pGEX-6p-1 and the resulting PCR product are digested with two restriction enzymes BamH I and Xho I. The vector carried the GST-tag affinity containing two restriction sites of BamH I and Xho I respectively. Finally, the double-digested target gene fragment and the plasmid vector are religated into a circular recombinant plasmid by T4 ligase.
The detection of recombinant plasmid is to preliminarily screen whether the recombinant plasmid is successfully transformed or not by using ampicillin resistance of the recombinant vector after the transformed plasmid into E. coli DH5a. After colony PCR, the nucleic acid gel electrophoresis is used to preliminarily verify whether the target fragment is ligated into the vector (as shown in
The specific expression and purification of E1 protein: recombinant plasmid pGEX-6p-1-N-GST is transformed into E. coli expression strain BL21 for protein expression. The above E. coli is cultured overnight in 11 mL LB medium containing 50 μg/mL ampicillin at 37° C. and 220 rpm. Then, 10 mL of culture solution is injected into 1 L of fresh LB medium containing 50 μg/ml ampicillin, and 0.5 mM (final concentration) IPTG (Isopropyl β-D-Thiogalactoside) is added to induct when the bacterial concentration reaches 0.6-0.8 units (OD600). After induction for 16 hours at 16° C., the bacteria are harvested by centrifugation at 4000 rpm for 20 minutes, and the suspension is resuspended in protein buffer 20 mM tris-HCl (pH 7.3), 200 mM NaCl. After the bacteria are broken by high pressure four times, the supernatant is harvested by centrifugation at 16000 rpm for 40 minutes. Then the supernatant is filtered through a 0.45 μm pore size filter and the target protein is purified by GST affinity chromatography. After the hybrid protein is eluted, the target protein is digested on the PSP enzyme column for 2 hours, and then the target protein is elute with protein buffer.
The purity of the target protein is high after purification by GST affinity chromatography. Finally, the molecular sieve is used to separate the polymer and the monomer, and the first peak protein is the pure E1. Simultaneously, from the analysis of the peak position of molecular sieve, the obtained E1 is in the form of hexamer, and the wild E1 form is very similar. The remaining protein samples are tested by polyacrylamide gel electrophoresis to meet the expected size.
The methods for gene cloning and expression purification of two mutants refers to wild type E1 (306-605), and the first appeared peak-tube after molecular sieve collection is the mutant E1. The remaining protein samples are tested by polyacrylamide gel electrophoresis compared with WT-E1 (306-605), since only one amino acid is mutated, the molecular weight of the mutant is very close to the WT-E1 (306-605) protein. Moreover, they are almost in a same position on the gel electrophoresis strip, as shown in
Fluorescently labeled truncated E1-2 (306-605) protein: The material used is a fluorine-labeled fluorescein isothiocyanate (FITC) conjugate kit (Sigma, St. Louis, Missouri). According to the kit description, the excess FITC is removed by column chromatography, and the FITC-linked E1 is eluted with protein buffer (20 mM tris-HCl (pH7.3), 200 mM NaCl). Verified FITC labels E1 (306-605) with SDS-PAGE (Figure omitted, the position of FITC labeled E1-2 on SDS-PAGE is slightly higher than that of unlabeled E1-2).
Preparation of vesicles (SUVs) containing truncated bodies E1-2 (306-605): In order to prepare vesicles of about 0.1 um in size containing E1 protein, 1 mg/mL of DOPC is add into a vial. The aqueous solution containing protein E1 (concentration about 0.5 mg/ml) is added after nitrogen blow dry the chloroform, then hydrates the lipid membrane to make suspension, and this suspension is further extruded by Mini squeezer (purchased from AVANTI Co. Ltd, America) through polycarbonate (PC) films (diameter of 100 nm) to produce protein-SUVs. The resulted SUVs can be stored at 4° C. for a short term and at −80° C. for a long term; Only the SUVs without labeled by fluorescence shows similar form to vesicles of the same size under optical microscope. (The resulted protein-SUVs by Mini squeezer have a good uniformity).
The procedure of preparing giant vesicles containing truncated E1-2 (306-605): meanwhile, giant vesicles labeled with fluorescence could also be prepared. Mixing 1 ml of DOPC (1 mg/ml) or 1 ml of DPHPC (1 mg/ml) and 1% of Texas Red (purchased from Thermofisher Co. Ltd, America) in a brown bottle; then drying chloroform by nitrogen, or volatilizing chloroform in rotary evaporator in this procedure; next, putting DOPC or DPHPC obtained from above step in vacuum drier overnight; In order to acquire hybrid giant unilamellar vesicles (GUVs) inserted E1 protein, adding 200-300 Mm of sucrose solution which containing E1 (concentration about 0.5 mg/ml) to hydrate the lipid molecular layer.
Those vesicles labeled with Texas Red can be observed in fluorescence microscope. To prepare fluorescence-labeled protein complexes embedded with vesicles, FITC-labeled E1-2 obtained from previous procedure can be used here. The result of observing GUVs in fluorescence microscope shows that the size of vesicles with larger diameter obtained by rotary evaporator is not as uniform as that of SUVs prepared by squeezer. Some vesicle protein complex with diameter over 50 μm are found in latter nanopore insertion with artificial membrane trail, and these vesicles easily ruptures bilayer lipid membrane (artificial lipid membrane is formed on the surface of 50 μm-diameter hole which made up of polyacetal resin, purchased from Warner Co. Ltd, America).
Conducting membrane fusion experiment on the mutant of truncated E1-2 with the same method, the result shows that, consistent with WT-E1 (306-605), this protein can also be steady inserted into the artificial lipid bilayer and PMOXA-PDMS-PMOXA triblock copolymer. The procedure of the experiment is similar to that of WT-E1 (306-605), when the GUVs inserted with mutant E1 is obtained, the protein embedding on the membrane is observed by Cryo-EM, and as shown in
The double-labeled vesicle-embedded protein complex (red as the Texas red labeled vesicles, and green as the FITC labeled E1-2 protein) is observed under fluorescence microscope, and it is found that some labeled E1-2 protein shows irregular positioning on vesicle membrane, part of the “transmembrane region” as expected is inserted into the phospholipid bilayer to form pores. This result also proves that in the conductance buffer, E1-2 can spontaneously aggregate on the artificial lipid membrane driven by voltage and can insert into the membrane in an expected direction to form a conductive pore.
Electrophysiological measurement: the instrument used in this embodiment is HEKA EPC-10 USB which integrates Amplifier and Digital-to-analog converter (DAC), and it has two electrodes named of pressure (voltage clamp) electrode and reference electrode, which are a pair of silver/silver chloride electrodes (Ag/AgCl). The instrument is used to measure the transmembrane current across both sides of the phospholipid bilayer. The sample frequency setup here is 2 kHz, and the frequency of low-pass filter is 1 kHz; the software Patch-master is used to collect the data, and Clampfit is utilized to analyze the collected data.
The fabrication of bilayer lipid membrane (BLM): The horizontal standard BLM fabricator and vertical standard BLM chamber (BCH-13A, purchased from Warner. Co. Ltd, America; Cups contain a 50 μm-diameter hole is custom made) are used to fabricate the BLM. A thin Teflon film with an aperture of 80-240 μm (TP-02 from Eastern Sci. LLC) and a Polyformaldehyde resin CUPS with an aperture of 50 μm are used as a partition to respectively separate BLM fabricator and BLM chamber into cis-compartment (working volume 250 μL) and trans-compartment (working volume 2.5 mL). After the aperture is pre-painted twice with 0.5 μL, 1 mg/ml of DOPC solution or DPHPC solution (the solvent is n-hexane) to ensure the complete coating of the entire edge of the aperture, the two compartments are filled with conducting buffers (5 mM Hepes/pH 7.5, with varying concentration of KCl solution, or PBS solution); Then, adding 25 mg/ml of DOPC solution or DPHPC solution (the solvent is n-hexane) near 50 μm aperture and it finds that the current falling from 10.2 nA to 0 pA.
The distribution of conductance of E1:
The vesicle-protein complex prepared previously forms a BLM embedded with E1-2 protein nanopore structure on the micropores of horizontal ptfe membrane (as described above) or vertical polyformaldehyde resin micropores.
The stock solution of vesicles/E1 complex prepared earlier is diluted by 10-20 times for the BLM experiments before use. For insertion of E1, around 2 μL of the diluted liposome solution is loaded into the cis-chamber; the other simple method is described below: a bubble containing some liposome at the pipette top is used to sweep the aperture gently in the cis-chamber, and the pore would form spontaneously. Conductance of E1 protein is measured in two methods: the first is under a constant transmembrane voltage (e.g. −70 mv), measuring current leap when multiple pores are embedded and dropped, and then counting data to calculate the distribution of conductance of pores. The second method is to apply a scanning voltage (e.g. −120 mv to 120 mv) to both sides of the membrane and calculate the pore conductance by calculating the rate of the current and voltage curve.
In this invention, large numbers of data are counted and the result demonstrates that, the single-pore conductance in 5 mM HEPES and 1 M KCl is around 1.34±0.07 nS (as shown in
The same trial on mutant E1 is conducted, and the result shows that under 0.5 M KCl, 10 Mm HEPES (pH 7.5), single-pore embedding causes about 75 pA of current ascending step when given a +100 mV bias voltage, as shown in
The study on the stability of the pore of E1-2: in this invention, the stability of pores of E1-2 and the mutant of E1 on phospholipids membrane and high voltage-gating phenomenon are studied under positive and negative voltage respectively. The results depicted: no gating phenomenon is found for E1 pore under positive 300 mV and negative 300 mV, and E1 pore could exist on the phospholipids membrane steadily when given a high voltage. At the same time, it is found that when there are too much glycerol in the conductance buffer (used to preserve E1 protein), the membrane embedded protein complex become abnormally unstable, and it is extremely easy for the protein to fall off from the membrane or the membrane to rupture directly.
In the stability experiment of E1 protein mutant (K421L, H323W) at high voltage, the scanning voltage of −300-300 mv is adopted. It finds that at a higher voltage (±300), the pore remained stable on the membrane, and the conductance distribution does not change significantly, showing that the mutant E1 (K421L, H323W) also has stable conductance characteristics as WT-E1 (306-605).
ssDNA used in this embodiment is 48 nt and purchased from Takara company, its detail sequence is depicted as below; The electrolyte is HEPES/1M KCl; In general, there are two methods to achieve nucleic acid transport under this condition.
Method 1: When E1 protein inserts into BLM, changing the voltage to 0 mV and adding the nucleic acids to be transported to the cis; Method 2: the nucleic acid to be transported is pre-mixed into the conductance buffer, and the cis and trans are mixed in the same amount. The translocation of DNA mainly depends on the applied transmembrane voltage. Without special instructions, method 1 is adopted for ssDNA translocation in this experiment, and the concentration of ssDNA in the translocation system is 100 nM/L.
In the case of the 48 nt ssDNA, the single-pore pore is embedded in the membrane, and the current blocking caused by translocation is about 65 picoamperes (transmembrane voltage is about 50 mv) (as shown in
Meanwhile, ssRNA translocation experiment is conducted like the ssDNA translocation experiment mentioned above. Noted that using DEPC solution and autoclave sterilization to prevent RNA degradation. The result shows that, similar to ssDNA translocation, ssRNA induced around 80% blockage, and under −50 mV the blocked current in PBS buffer system is about 8 pA, the dwell time is 1-2 ms.
As a comparison, the current trace in the system without nucleic acid but with only pores are static. One advantage of this pore is that the static current in the control group rarely interferes with the non-specific blocking. In the experiment, when nucleic acid premixed into the conductance buffer, amounts of translocation instantly found after the first insertion of the protein pore into the phospholipid membrane, and the blocking phenomenon becomes less and less. This result shows that when there is no stirring equipment in the sample tank, the occurrence of DNA translocation is delayed.
E1 protein mutant is translocated by ssDNA/ssRNA using the same conductance conditions and single stranded nucleic acid. Under the conductance condition of 1M KCl and 10 mM Hepes (pH7.5), applying the bias voltage of 120 mv, it finds that the blocking rate of ssDNA translocation is close to 78%, and the translocation time is close to 0.5 ms (as shown in
The double-stranded DNA (dsDNA) obtained from BamH1 enzyme is added to the cis-chamber, and the translocation buffer is 10 mM HEPES/1M KCl with ssDNA. The transfer signals are detected at 50 mv, 70 mv, 120 mv and 150 mv voltages respectively, and no dsDNA translocation is observed.
Q-PCR is used to make the standard curve of nucleic acid amplification: dsDNA is prepared from annealing two ssDNA (80nt) and identified with 2% agarose gel, and extracted from gel. The concentration of dsDNA extracted from gel is determined by Qubit®3.0 (Thermo fisher scientific Co. Ltd, America) (This method is better than ultraviolet spectrophotometer in accuracy and precision); The resulting dsDNA of known concentration is diluted into 10 of 10-time concentration gradients, and then using Q-PCR (Premix SYBR-Takara Co. Ltd, Japan) to make the standard curve for the ct value of dsDNA concentration, so as to obtain the standard correlation (as shown in
Quantitative analysis of ssDNA through pore by Q-PCR, as mentioned above, after E1 protein embedded into the membrane in cis-chamber, adding 50 nM 80 nt-DNA (the first method), or premixing 25 nM 48 nt-DNA into conductance buffers at both side chambers (the second method). As a negative control, 50 nM 80nt-DNA is added to cis-chamber without E1 protein, or the equivalent amount of 25 nM 80nt-DNA is added to both side chambers. Applying a voltage of −70 mV to both sides of the membrane and collecting two-chambers' conductance buffer for Q-PCR quantitative analysis after 10 min, 20 min, 40 min, 60 min and 90 min, respectively.
All nucleic acids involved in translocation experiments are described below: (purchased from Takara, Co. Ltd, Japan)
Labeled nucleic acid chain and labeled nucleic acid chain 1 are described as SEQ ID No. 20 and SEQ ID No. 21:
The sequences of dsDNA and dsDNA1 with dspacer (dspacer is a nucleotide having only a phosphate skeleton and no bases, therefor its spatial structure is smaller than normal nucleotides) are shown in SEQ ID No. 22 (three dspacer are inserted between the eleventh and twelfth bits) (the detail sequence is 5′-TTTTTTTTTTT XXXTTTTTTTTTTT-3′, and X represents dspacer) and SEQ ID No. 23:
The sequence of nucleic acid used in quantitative translocation analysis by Q-PCR are shown in SEQ ID No. 24 and SEQ ID No. 25:
The two primers (primer 1 and primer 2) used for quantitative translocation by Q-PCR are shown in SEQ ID no.26 and SEQ ID no.27, respectively:
The annealing procedure of dsDNA is performed at PCR equipment, the annealing temperature is 95° C., and the annealing time is set up to 2 min; then the process of cooling is set up to gradient (almost 1° C./min), which lasts 1 h and 20 min. Lastly, the nucleic acid product is determined by agarose gel (as shown in
In this invention, dsDNA is acquired from circular plasmid Hag-C1 digested by BamH1, and it is purified by QIAGEN DNA purification kit the product 3800 bp dsDNA was conducted by QIAGEN DNA purification kit (QIAGEN, Co. Ltd, Germany).
The invention using E1 (306-577) to verify the helical activity of ds DNA of the protein hexamer in vitro.
The buffer solution in helicase experiment is 20 mM HEPES (pH 7.5), 0.7 mg/ml BSA, 5% Glycerol, 5 mM MgCl2, 3 mM DTT; And the reaction is initiated by adding 2 mM ATP; the substrate dsDNA in this trial is 22 bp labeled with 5′-fluor and 3′-quencher at the terminals of DNA which could form hairpin spontaneously.
In vitro, dsDNA ends flat cannot be directly unwind by this helicase due to the lack of other protein components contained in the virus itself to assist in DNA replication.
Synthesized dsDNA with a single stranded arm is used in the unwinding experiment in vitro and unwinding experiment on membrane mentioned later. E1 protein unwinding starts with the single-arm nucleic acid strand entering the pore. In the process of unwinding, excitation wavelength is 643 nm and emission wavelength is 667 nm, Multifunctional fluorescence microplate reader (Bio-Tek, Co. Ltd, America) is used to continuously monitor the fluorescence of the substrate (5 nM nucleic acid substrate) in the reaction system to visually observe the unwinding process. When dsDNA is unwound, one of the ssDNA terminal forms spontaneously hairpin structure, and fluorescence tag could be quenched by quencher tag.
The result demonstrates that, E1-2 has helicase activity in vitro, double-stranded nucleic acids can be unwound in the presence of ATP, as shown in
After verifying the helicase activity of E1 in vitro, unwinding experiments on the artificial lipid membrane is planned: after insertion of E1 into the BLM, dsDNA could not be translocation through the E1 protein at the room temperature (21° C.) in the absence of ATP and Mg2+ because of the diameter of double-stranded DNA is larger than the diameter of E1 protein pore (as mentioned above).
However, by controlling the appropriate system environment, including the concentration of ATP, Mg2+ concentrations, and system temperature, dsDNA translocation through E1 is observed at the molecular level (as shown in
Because low salt concentration is needed in E1 helicase activity determination experiments, PBS is chosen to conduct the unwinding on the artificial lipid membrane; in this buffer solution, the conductance of E1-2 is about 0.2±0.02 nS.
The scheme of this experiment is described below: After BLM is formed in PBS conductance buffer, E1-2 steady inserts into BLM (as described above); then dsDNA (final concentration of 12.5 nM) is added into cis-chamber and heats up the conductance buffer with a heating plate to 37° C.; then ATP (final concentration of 5 mM) and Mg2+ (final concentration of 5 mM) are added into the conductance buffer.
The result displays that, with ATP hydrolysis, dsDNA is unwound as ssDNA by E1-2 embedded in the BLM and is translocated from cis- to trans-side. Under −40 mV, amounts of dsDNA unwinding phenomenon are observed and pores will keep blockage as the voltage is reversed to +40 mV. However, with voltage changing from +40 mV to −50 mV, the unwinding occurs again and it restarts from the blocked state (as shown in
dsDNA with Different Lengths Unwinding on Membrane:
Moreover, the invention explores the unwinding phenomenon of dsDNA with different lengths on the artificial lipid membrane.
Recombinant plasmid PET-28b+MspA is digested with XhoI and EcoO109I to five different lengths of fragments; Since both enzymes can digests linear double strands with sticky ends, dsDNA has an extended single arm (the length is 5 bp, for the reasons mentioned above), so dsDNA with 5 different lengths is used to explore the influence of different strand's lengths on unwinding on the membrane, and the experimental process is the same as above
The results show that, under the same other conditions, with the increase of strand's length, the unwinding time of E1-2 also increases proportionally. As shown in
dsDNA Unwinding on Membrane at Different Temperatures:
On the other hand, this invention attempts to observe the unwinding phenomenon of dsDNA on the membrane under same conditions except different temperatures. The experiments of 24 bp nucleic acid strand mentioned above are conducted at gradient temperatures, respectively, room temperature (21° C.), lower than 35° C., 35° C. −37° C., and higher than 37° C.,
The results show that the frequency of unwinding increases proportionally with the increase of temperature, but when the temperature is higher than 37° C., the unwinding begins to decrease, which is consistent with the characteristics of E1-2 as a viral helicase (as shown in
dsDNA Unwinding on Membrane at Different Transmembrane Voltages:
This invention also determines the time required for E1-2 unwinding the same dsDNA substrate at different transmembrane voltages, and the experimental process is the same as above mentioned.
The experimental results show that with nucleic acid substrate mixing into the cis-chamber, the unwinding time is extended accordingly when the absolute voltage value is gradually reduced at negative voltage, and a non-linear function is fitted with the voltage gradient and unwinding time. The resulting curve is oriented towards the axis, which shows and proves that in addition to the driving force of voltage, E1-2 is also actively unwinding, and the direction of the two forces is the same. As shown in
The Unwinding of Special Nucleic Acid Substrate on Membrane:
This invention also designs another special nucleic acid substrate with three dspacers (without bases) in one strand of dsDNA, which has single arm and consists of A and T. The unwinding experiment is conducted with this special nucleic acid substrate.
It founds that in normal unwinding signal, small steps with a size of 20-30 pA appears at specific locations. And the specific locations of small step signals are consistent with those of the dspacers in nucleic acid.
Verifying E1 Unwinding on Membrane (Depending on the Function of Mg2+ and ATP):
To verify the unwinding of E1-2 on membrane, excess EDTA which chelated with Mg2+ is applied to inactivate the helicase. The experimental process is the same as the above mentioned. In the process of unwinding, excess of EDTA chelator is added to the reaction system.
The results show that with the increase of EDTA, the unwinding activity is gradually inhibited, and the maximum inhibition efficiency reaches to more than 80%. When excess Mg2+ is added to the reaction system, it is clearly observed that the unwinding reappears, recovering to maximum efficiency by ½ or more.
At the same time, when ATPαS, another analog of ATP, is used to competitively replace ATP in the unwinding system, it is found that ATPαS could not hydrolyze to supply energy like ATP, the unwinding activity on membrane is significantly inhibited. Because this inhibition is not as reversible as EDTA chelating Mg2+, when excess ATPαS is added, the unwinding activity on membrane gradually disappears.
Studying the unwinding of E1 mutants on artificial lipid membranes with the same experimental methods and conditions, it is found that the translocation of mutant of E1 protein is initiated by 2 mM ATP. The unwinding signal similar to WT-E1 (306-605) is observed at a bias voltage of −100 mV, as shown in
The above results show that, for the first time, a cyclic hexameric helicase of bovine papilloma virus has been successfully engineered into a protein nanopore, which is embedded in lipid bilayer membrane and polymer membrane. The Nanopore can stably stay on lipid bilayer without gating at high voltage. And it still keeps the characteristics of a helicase on artificial lipid membranes, such as temperature specificity, and competitive inhibition by ATP analogues. This nanopore can passively translocate single-stranded RNA as well as single-stranded DNA on membrane. And dsDNA with a single arm can be unwound on membrane using energy supplied by ATP hydrolysis, with the unwinding time positively proportional to the length of substrate.
The above experiments show that this invention innovatively discovers two proteins E1-1 (306-577) and E1-2 (306-605), wherein the former can be used as a new simple membrane containing conductive pore, and it can insert into lipids bilayer stably and translocation nucleic acid, the latter further has dual effects of nanopore and helicase. This invention constructs a sensing system combining the characteristics of nanopore and helicase, which replaces the existing sensing method requiring helicase a coupling nanopore, and has a good application prospect.
Further, this invention also creatively studies the mutant of E1-2 protein, obtains mutants of E1-2. It is found that the nanopore constructed by mutated monomer is more likely to capture nucleic acids and other negatively charged small molecules than the wild type protein. In addition, the mutated protein shows an increase in current range, which makes the inner cavity of the pore narrower than that of the wild type, so that the current detection of the pore is more extensive and sensitive.
| Number | Date | Country | Kind |
|---|---|---|---|
| 201710060033.9 | Jan 2017 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2018/073716 | 1/23/2018 | WO |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2018/137592 | 8/2/2018 | WO | A |
| Number | Date | Country |
|---|---|---|
| 102902895 | Jan 2013 | CN |
| 104710519 | Jun 2015 | CN |
| 2768977 | Sep 2015 | EP |
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| Number | Date | Country | |
|---|---|---|---|
| 20190383790 A1 | Dec 2019 | US |
